Melanocytic nevi and melanoma: unraveling a complex relationship
暂无分享,去创建一个
[1] R. Botella-Estrada,et al. Study of the Immunophenotype of the Inflammatory Cells in Melanomas With Regression and Halo Nevi , 2015, The American Journal of dermatopathology.
[2] Simon Tavaré,et al. Autophagy mediates the mitotic senescence transition. , 2009, Genes & development.
[3] O. C. Stegmaier. Natural regression of the melanocytic nevus. , 1959, The Journal of investigative dermatology.
[4] C. Gross,et al. County‐level association of melanoma and papillary thyroid cancer: evidence of shared environmental risk? , 2015, Pigment cell & melanoma research.
[5] J. Larkin,et al. Combination dabrafenib and trametinib in the management of advanced melanoma with BRAFV600 mutations , 2016, Expert opinion on pharmacotherapy.
[6] K. Duffy,et al. The dysplastic nevus: from historical perspective to management in the modern era: part I. Historical, histologic, and clinical aspects. , 2012, Journal of the American Academy of Dermatology.
[7] Jing Chen,et al. Tyrosine Phosphorylation Inhibits PKM2 to Promote the Warburg Effect and Tumor Growth , 2009, Science Signaling.
[8] C. Johannessen,et al. A negative feedback signaling network underlies oncogene-induced senescence. , 2006, Cancer cell.
[9] D. Schadendorf,et al. Highly Recurrent TERT Promoter Mutations in Human Melanoma , 2022 .
[10] D. Peeper,et al. Oncogene-Induced Senescence Relayed by an Interleukin-Dependent Inflammatory Network , 2008, Cell.
[11] Abraham J. Khorasani,et al. Loss of 5-Hydroxymethylcytosine Is an Epigenetic Hallmark of Melanoma , 2012, Cell.
[12] L. Hayflick,et al. The serial cultivation of human diploid cell strains. , 1961, Experimental cell research.
[13] Masaaki Komatsu,et al. Autophagy: Renovation of Cells and Tissues , 2011, Cell.
[14] R. Banks. Oncogene‐induced cellular senescence elicits an anti‐Warburg effect , 2013, Proteomics.
[15] Lyndon Su,et al. Expression of gamma-H2AX in melanocytic lesions. , 2008, Human pathology.
[16] E. Medrano,et al. Dynamic assembly of chromatin complexes during cellular senescence: implications for the growth arrest of human melanocytic nevi , 2007, Aging cell.
[17] P. Puigserver,et al. PGC1α expression defines a subset of human melanoma tumors with increased mitochondrial capacity and resistance to oxidative stress. , 2013, Cancer cell.
[18] A. Benner,et al. PTEN/MMAC1 expression in melanoma resection specimens , 2002, British Journal of Cancer.
[19] K. Flaherty,et al. Marked, homogeneous, and early [18F]fluorodeoxyglucose-positron emission tomography responses to vemurafenib in BRAF-mutant advanced melanoma. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] F. Silvestris,et al. miRNAs in melanoma: a defined role in tumor progression and metastasis , 2016, Expert review of clinical immunology.
[21] R. Parwaresch,et al. Enhanced expression of Ki-67, topoisomerase IIalpha, PCNA, p53 and p21WAF1/Cip1 reflecting proliferation and repair activity in UV-irradiated melanocytic nevi. , 1998, Human pathology.
[22] M. Karin,et al. Immunity, inflammation, and cancer: an eternal fight between good and evil. , 2015, The Journal of clinical investigation.
[23] R. Sager. Senescence as a mode of tumor suppression. , 1991, Environmental health perspectives.
[24] B. Dumitriu,et al. Telomere dynamics in mice and humans. , 2013, Seminars in hematology.
[25] S. Dry,et al. Changes in size of melanocytic nevi during pregnancy. , 1997, Journal of the American Academy of Dermatology.
[26] M. Martinka,et al. eIF4E is an adverse prognostic marker of melanoma patient survival by increasing melanoma cell invasion. , 2015, The Journal of investigative dermatology.
[27] P. Ms,et al. PROTECTION AGAINST RUBELLA , 1965 .
[28] B. Bastian,et al. From melanocytes to melanomas , 2016, Nature Reviews Cancer.
[29] N. Hayward,et al. Cutaneous melanoma susceptibility and progression genes. , 2005, Cancer letters.
[30] B. Vogelstein,et al. Variation in cancer risk among tissues can be explained by the number of stem cell divisions , 2015, Science.
[31] H. Kluger,et al. Genetic inactivation or pharmacological inhibition of Pdk1 delays development and inhibits metastasis of BrafV600E::Pten−/− melanoma , 2013, Oncogene.
[32] Blake Ferguson,et al. A blueprint for staging of murine melanocytic lesions based on the Cdk4 R24C/R24C ::Tyr‐ NRAS Q 61K model , 2012, Experimental dermatology.
[33] Steven J. M. Jones,et al. Genomic Classification of Cutaneous Melanoma , 2015, Cell.
[34] Xu Dong Zhang,et al. ER stress‐induced autophagy in melanoma , 2015, Clinical and experimental pharmacology & physiology.
[35] M. Bosenberg,et al. DNMT3b Modulates Melanoma Growth by Controlling Levels of mTORC2 Component RICTOR. , 2016, Cell reports.
[36] P. Tschandl,et al. Impact of oncogenic BRAF mutations and p16 expression on the growth rate of early melanomas and naevi in vivo , 2016, The British journal of dermatology.
[37] J. Utikal,et al. Extra c-myc oncogene copies in high risk cutaneous malignant melanoma and melanoma metastases , 2001, British Journal of Cancer.
[38] Carlos Cordon-Cardo,et al. Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas , 2007, Nature.
[39] O. Larsson,et al. Expression of Insulin-Like Growth Factor-1 Receptor (IGF-1R) and p27Kip1 in Melanocyte Tumors: A Potential Regulatory Role of IGF-1 Pathway in Distribution of p27Kip1 between Different Cyclins , 2000, Growth factors.
[40] P. Meltzer,et al. High frequency of BRAF mutations in nevi , 2003, Nature Genetics.
[41] D. Wong,et al. p16INK4a expression is frequently decreased and associated with 9p21 loss of heterozygosity in sporadic melanoma , 1998, Journal of cutaneous pathology.
[42] Simon Tavaré,et al. Spatial Coupling of mTOR and Autophagy Augments Secretory Phenotypes , 2011, Science.
[43] M. Martinka,et al. Prognostic significance of activated Akt expression in melanoma: a clinicopathologic study of 292 cases. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[44] Y. H. Yang,et al. Reduced p16 and Increased Cyclin D1 and pRb Expression Are Correlated With Progression in Cutaneous Melanocytic Tumors , 2009, International journal of surgical pathology.
[45] B. Bastian. Understanding the progression of melanocytic neoplasia using genomic analysis: from fields to cancer , 2003, Oncogene.
[46] M. Landthaler,et al. The absence of BRAF, FGFR3, and PIK3CA mutations differentiates lentigo simplex from melanocytic nevus and solar lentigo. , 2009, The Journal of investigative dermatology.
[47] P. Boyle,et al. Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. , 2005, European journal of cancer.
[48] Ru Wei,et al. The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth , 2008, Nature.
[49] Benjamin G. Bitler,et al. Suppression of nucleotide metabolism underlies the establishment and maintenance of oncogene-induced senescence. , 2013, Cell reports.
[50] T. Spector,et al. Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi , 2009, Nature Genetics.
[51] W. Mooi,et al. Oncogene-induced Cellular Senescence , 2010, Advances in anatomic pathology.
[52] R. MacKie,et al. The number and distribution of benign pigmented moles (melanocytic naevi) in a healthy British population , 1985, The British journal of dermatology.
[53] P. Nowell,et al. Characteristics of cultured human melanocytes isolated from different stages of tumor progression. , 1985, Cancer research.
[54] A. Brożyna,et al. The role of melanogenesis in regulation of melanoma behavior: melanogenesis leads to stimulation of HIF-1α expression and HIF-dependent attendant pathways. , 2014, Archives of biochemistry and biophysics.
[55] S. Lowe,et al. p53-dependent chemokine production by senescent tumor cells supports NKG2D-dependent tumor elimination by natural killer cells , 2013, The Journal of experimental medicine.
[56] N. Ibrahim,et al. Melanocytic nevus-like hyperplasia and melanoma in transgenic BRAFV600E mice , 2009, Oncogene.
[57] S. Lowe,et al. Rb-Mediated Heterochromatin Formation and Silencing of E2F Target Genes during Cellular Senescence , 2003, Cell.
[58] R. Barr. Deep penetrating nevus. , 1997, Dermatology online journal.
[59] R. Scolyer,et al. BRAF Inhibition Decreases Cellular Glucose Uptake in Melanoma in Association with Reduction in Cell Volume , 2015, Molecular Cancer Therapeutics.
[60] J. Schaffer. Update on melanocytic nevi in children. , 2015, Clinics in dermatology.
[61] H. Chu,et al. DNA-methylation profiling distinguishes malignant melanomas from benign nevi , 2011, Pigment cell & melanoma research.
[62] A. Alimonti,et al. Tumour-infiltrating Gr-1+ myeloid cells antagonize senescence in cancer , 2014, Nature.
[63] W. Black. Residual dysplastic and other nevi in superficial spreading melanoma. Clinical correlations and association with sun damage , 1988, Cancer.
[64] Stephen B Gruber,et al. BRAF and NRAS mutations in melanoma and melanocytic nevi , 2006, Melanoma research.
[65] J. Grichnik,et al. Early melanoma detection: nonuniform dermoscopic features and growth. , 2003, Journal of the American Academy of Dermatology.
[66] S. Florell,et al. A Decade of Melanomas: Identification of Factors Associated with Delayed Detection in an Academic Group Practice , 2011, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].
[67] B. Higgins,et al. BRAFV600E Negatively Regulates the AKT Pathway in Melanoma Cell Lines , 2012, PloS one.
[68] M. N. Epstein,et al. A study of tumor progression: the precursor lesions of superficial spreading and nodular melanoma. , 1984, Human pathology.
[69] C. Lian,et al. TET2 Negatively Regulates Nestin Expression in Human Melanoma. , 2016, The American journal of pathology.
[70] A. Morris,et al. Cancer etiology. Variation in cancer risk among tissues can be explained by the number of stem cell divisions , 2015, BDJ.
[71] W. Stolz,et al. Ultrastructural discrimination between malignant melanomas and benign nevocytic nevi using high-resolution image and multivariate analyses. , 1991, The Journal of investigative dermatology.
[72] J. Wilmott,et al. Concordant BRAFV600E mutation status in primary melanomas and associated naevi: implications for mutation testing of primary melanomas , 2014, Pathology.
[73] Hong Wu,et al. mTOR is activated in the majority of malignant melanomas. , 2008, The Journal of investigative dermatology.
[74] K. Brown,et al. PDK1 and SGK3 Contribute to the Growth of BRAF-Mutant Melanomas and Are Potential Therapeutic Targets. , 2015, Cancer research.
[75] J. Radhi. Malignant Melanoma Arising from Nevi, p53, p16, and Bcl-2: Expression in Benign versus Malignant Components , 1999, Journal of cutaneous medicine and surgery.
[76] H. Simon,et al. Down-Regulation of Autophagy-Related Protein 5 (ATG5) Contributes to the Pathogenesis of Early-Stage Cutaneous Melanoma , 2013, Science Translational Medicine.
[77] M. Held,et al. A role for the JARID1B stem cell marker for continuous melanoma growth , 2010, Pigment cell & melanoma research.
[78] H. Kerl,et al. Proliferation antigens in cutaneous melanocytic tumors--an immunohistochemical study comparing the transferrin receptor and the Ki 67 antigen. , 1989, Dermatologica.
[79] Hyun-Jeong Leea,et al. Melanocytic nevus with pregnancy-related changes in size accompanied by apoptosis of nevus cells: A case report , 2000 .
[80] M. Mytilinaiou,et al. Heparan sulfate proteoglycans and heparin regulate melanoma cell functions. , 2014, Biochimica et biophysica acta.
[81] W. Black. Residual dysplastic and other nevi in superficial spreading melanoma. Clinical correlations and association with sun damage. , 1989, Cancer.
[82] Tammie C. Ferringer. Update on immunohistochemistry in melanocytic lesions. , 2012, Dermatologic clinics.
[83] P. Carli,et al. Eruptive melanocytic nevi in patients with renal allografts: report of 10 cases with dermoscopic findings. , 2003, Journal of the American Academy of Dermatology.
[84] M. Hussein,et al. Immunohistological characterisation of tumour infiltrating lymphocytes in melanocytic skin lesions , 2006, Journal of Clinical Pathology.
[85] J. Campisi,et al. The senescence-associated secretory phenotype: the dark side of tumor suppression. , 2010, Annual review of pathology.
[86] G. Mcneer. MALIGNANT MELANOMA. , 1965, Surgery, gynecology & obstetrics.
[87] M. Mihm,et al. BAP1 and BRAFV600E expression in benign and malignant melanocytic proliferations. , 2015, Human pathology.
[88] Kelly J. Morris,et al. A complex secretory program orchestrated by the inflammasome controls paracrine senescence , 2013, Nature Cell Biology.
[89] L. Chin,et al. p16(Ink4a) in melanocyte senescence and differentiation. , 2002, Journal of the National Cancer Institute.
[90] D. Massi,et al. Beclin 1 and LC3 autophagic gene expression in cutaneous melanocytic lesions. , 2010, Human pathology.
[91] Peter Kraft,et al. Identification of Novel Genetic Markers of Breast Cancer Survival , 2015, Journal of the National Cancer Institute.
[92] Jianxin Shi,et al. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma , 2014, Nature Genetics.
[93] J. Reis-Filho,et al. Oncogenic Braf induces melanocyte senescence and melanoma in mice. , 2009, Cancer cell.
[94] D. Lange,et al. JARID1B expression in human melanoma and benign melanocytic skin lesions , 2013, Melanoma research.
[95] V. Klump,et al. Autophagy in cutaneous malignant melanoma , 2010, Journal of cutaneous pathology.
[96] S. Leow,et al. Telomerase regulates MYC-driven oncogenesis independent of its reverse transcriptase activity. , 2015, The Journal of clinical investigation.
[97] R. Marais,et al. Cellular senescence in naevi and immortalisation in melanoma: a role for p16? , 2006, British Journal of Cancer.
[98] J. Bruijn,et al. The extracellular matrix in pigmented skin lesions: an immunohistochemical study , 1994, Histopathology.
[99] D. Bennett,et al. Isolation, Culture, and Transfection of Melanocytes , 2014, Current protocols in cell biology.
[100] J. Arrese,et al. Ipilimumab induces simultaneous regression of melanocytic naevi and melanoma metastases , 2013, Clinical and experimental dermatology.
[101] Blake Ferguson,et al. Three‐dimensional modelling for estimation of nevus count and probability of nevus–melanoma progression in a murine model , 2014, Pigment cell & melanoma research.
[102] H. Simon,et al. Autophagy suppresses melanoma tumorigenesis by inducing senescence , 2014, Autophagy.
[103] H. Rui,et al. Suppression of Type I Interferon Signaling Overcomes Oncogene-Induced Senescence and Mediates Melanoma Development and Progression. , 2016, Cell reports.
[104] L. Thomas,et al. Melanoma patients under vemurafenib: prospective follow-up of melanocytic lesions by digital dermoscopy. , 2014, The Journal of investigative dermatology.
[105] P. Tschandl,et al. NRAS and BRAF Mutations in Melanoma-Associated Nevi and Uninvolved Nevi , 2013, PloS one.
[106] L. Cannon-Albright,et al. Longitudinal assessment of the nevus phenotype in a melanoma kindred. , 2004, The Journal of investigative dermatology.
[107] Lukas D. Osborne,et al. HIF1α and HIF2α independently activate SRC to promote melanoma metastases. , 2013, The Journal of clinical investigation.
[108] J. Cheng,et al. Deregulated Akt3 Activity Promotes Development of Malignant Melanoma , 2004, Cancer Research.
[109] A. García‐Díez,et al. Implication of MT1‐MMP in the maturation steps of benign melanocytic nevi , 2006, Journal of cutaneous pathology.
[110] A. Hauschild,et al. Telomerase activity in melanocytic lesions: A potential marker of tumor biology. , 2000, The American journal of pathology.
[111] James M. Roberts,et al. Cooperative Regulation of the Cell Division Cycle by the Protein Kinases RAF and AKT , 2004, Molecular and Cellular Biology.
[112] B. Bastian. Hypothesis: a role for telomere crisis in spontaneous regression of melanoma. , 2003, Archives of dermatology.
[113] R. Fisher,et al. High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[114] A. Sivachenko,et al. A Landscape of Driver Mutations in Melanoma , 2012, Cell.
[115] R. Camp,et al. Punctate LC3B Expression Is a Common Feature of Solid Tumors and Associated with Proliferation, Metastasis, and Poor Outcome , 2011, Clinical Cancer Research.
[116] T. Luedde,et al. Senescence surveillance of pre-malignant hepatocytes limits liver cancer development , 2011, Nature.
[117] M. Skolnick,et al. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus , 1994, Nature Genetics.
[118] K. Hou‐Jensen,et al. The presence of dysplastic nevus remnants in malignant melanomas. A population-based study of 551 malignant melanomas. , 1991, The American Journal of dermatopathology.
[119] G. Barsh,et al. Frequent somatic mutations of GNAQ in uveal melanoma and blue naevi , 2010 .
[120] S. Haferkamp,et al. Oncogene-induced senescence does not require the p16(INK4a) or p14ARF melanoma tumor suppressors. , 2009, The Journal of investigative dermatology.
[121] B. Bastian. The molecular pathology of melanoma: an integrated taxonomy of melanocytic neoplasia. , 2014, Annual review of pathology.
[122] S. Sánchez-Sosa,et al. Immunophenotypic characterization of lymphoid cell infiltrates in vitiligo , 2013, Clinical and experimental immunology.
[123] M. Hande,et al. Oncogene-induced telomere dysfunction enforces cellular senescence in human cancer precursor lesions , 2012, The EMBO journal.
[124] J. Campisi. Aging, cellular senescence, and cancer. , 2013, Annual review of physiology.
[125] T. Steiniche,et al. In‐situ hybridization‐based quantification of hTR: a possible biomarker in malignant melanoma , 2015, Histopathology.
[126] I. Yeh,et al. Clonal BRAF mutations in melanocytic nevi and initiating role of BRAF in melanocytic neoplasia. , 2013, Journal of the National Cancer Institute.
[127] R. M. Mackie,et al. Point mutations in the N‐ras oncogene in malignant melanoma and congenital naevi , 1994, The British journal of dermatology.
[128] J. Shay,et al. BRAFE600-associated senescence-like cell cycle arrest of human naevi , 2005, Nature.
[129] J. Taube,et al. Diagnostic utility of 5‐hydroxymethylcytosine immunohistochemistry in melanocytic proliferations , 2015, Journal of cutaneous pathology.
[130] M. Nasr,et al. Comparison of pHH3, Ki-67, and Survivin Immunoreactivity in Benign and Malignant Melanocytic Lesions , 2008, The American Journal of dermatopathology.
[131] M. Bosenberg,et al. Epigenetic silencing of novel tumor suppressors in malignant melanoma. , 2006, Cancer research.
[132] D. Peeper,et al. The essence of senescence. , 2010, Genes & development.
[133] D. Jiménez-Gallo,et al. Eruptive melanocytic nevi in a patient undergoing treatment with sunitinib. , 2013, JAMA dermatology.
[134] M. Fukayama,et al. Clonality in nevocellular nevus and melanoma: an expression-based clonality analysis at the X-linked genes by polymerase chain reaction. , 1997, The Journal of investigative dermatology.
[135] K. Hemminki,et al. TERT promoter mutations in cancer development. , 2014, Current opinion in genetics & development.
[136] M. Schultzberg,et al. Interleukin (IL)-1 alpha- and -1 beta-, IL-6-, and tumor necrosis factor-alpha-like immunoreactivities in human common and dysplastic nevocellular nevi and malignant melanoma. , 1995, The American Journal of dermatopathology.
[137] B. Bastian. The longer your telomeres, the larger your nevus? , 2003, The American Journal of dermatopathology.
[138] R. Scolyer,et al. Activation of the extracellular signal regulated kinase (ERK) pathway in human melanoma , 2005, Journal of Clinical Pathology.
[139] R. Marais,et al. G12DNRAS and kinase‐dead BRAF cooperate to drive naevogenesis and melanomagenesis , 2014, Pigment cell & melanoma research.
[140] S. Mannava,et al. Depletion of deoxyribonucleotide pools is an endogenous source of DNA damage in cells undergoing oncogene-induced senescence. , 2013, The American journal of pathology.
[141] Rajiv Kumar,et al. RICTOR involvement in the PI3K/AKT pathway regulation in melanocytes and melanoma , 2015, Oncotarget.
[142] Matthew J. Davis,et al. Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma , 2012, Nature Genetics.
[143] Rugang Zhang,et al. Activation of the PIK3CA/AKT pathway suppresses senescence induced by an activated RAS oncogene to promote tumorigenesis. , 2011, Molecular cell.
[144] S. Ryeom,et al. Detection of Oncogene-Induced Senescence In Vivo. , 2017, Methods in molecular biology.
[145] P. Nelson,et al. MTOR regulates the pro-tumorigenic senescence-associated secretory phenotype by promoting IL1A translation , 2015, Nature Cell Biology.
[146] E. Hersh,et al. Active immunotherapy with B.C.G. for recurrent malignant melanoma. , 1973, Lancet.
[147] L. Hayflick. THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS. , 1965, Experimental cell research.
[148] Jun S. Song,et al. Oncogenic BRAF regulates oxidative metabolism via PGC1α and MITF. , 2013, Cancer cell.
[149] M. Stratton,et al. High burden and pervasive positive selection of somatic mutations in normal human skin , 2015, Science.
[150] Pietro Rubegni,et al. Melanocytic skin lesions and pregnancy: digital dermoscopy analysis , 2007, Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging.
[151] K. Duffy,et al. The dysplastic nevus: from historical perspective to management in the modern era: part II. Molecular aspects and clinical management. , 2012, Journal of the American Academy of Dermatology.
[152] M. Schultzberg,et al. Interleukin (IL)-1α- and -1β-, IL-6-, and Tumor Necrosis Factor-α-like Immunoreactivities in Human Common and Dysplastic Nevocellular Nevi and Malignant Melanoma , 1995 .
[153] S. Haferkamp,et al. IGFBP7 Is Not Required for B-RAF-Induced Melanocyte Senescence , 2010, Cell.
[154] T. Giordano,et al. C-MYC overexpression is required for continuous suppression of oncogene-induced senescence in melanoma cells , 2008, Oncogene.
[155] T. Papp,et al. Mutational analysis of the BRAF gene in human congenital and dysplastic melanocytic naevi , 2005, Melanoma research.
[156] Sameer Gupta,et al. Genetics of melanocytic nevi , 2015, Pigment cell & melanoma research.
[157] Jashin J. Wu,et al. Melanoma in patients with chronic lymphocytic leukemia and non-Hodgkin lymphoma. , 2015, Journal of the American Academy of Dermatology.
[158] Jeffrey E. Lee,et al. Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 , 2011, Nature Genetics.
[159] J. Sedivy,et al. Expression of catalytically active telomerase does not prevent premature senescence caused by overexpression of oncogenic Ha-Ras in normal human fibroblasts. , 1999, Cancer research.
[160] R. Sager,et al. Suppression of tumor growth by senescence in virally transformed human fibroblasts. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[161] R. Sturm,et al. BRAFV600E mutation status of involuting and stable nevi in dabrafenib therapy with or without trametinib. , 2014, JAMA dermatology.
[162] T. Brenn,et al. Differential expression of microRNAs during melanoma progression: miR-200c, miR-205 and miR-211 are downregulated in melanoma and act as tumour suppressors , 2012, British Journal of Cancer.
[163] S. Florell,et al. Comparative Analysis of Total Body and Dermatoscopic Photographic Monitoring of Nevi in Similar Patient Populations at Risk for Cutaneous Melanoma , 2010, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].
[164] Z. Kefalopoulou,et al. Epigenetic Modifications in Cutaneous Malignant Melanoma: EZH2, H3K4me2, and H3K27me3 Immunohistochemical Expression is Enhanced at the Invasion Front of the Tumor , 2015, The American Journal of dermatopathology.
[165] B. Garcia,et al. The histone variant macroH2A suppresses melanoma progression through regulation of CDK8 , 2010, Nature.
[166] G. Wahl,et al. DNA damage triggers a prolonged p53-dependent G1 arrest and long-term induction of Cip1 in normal human fibroblasts. , 1994, Genes & development.
[167] Y. Maida,et al. Telomerase reverse transcriptase moonlights: Therapeutic targets beyond telomerase , 2015, Cancer science.
[168] D. DiMaio,et al. Senescence‐associated β‐galactosidase is lysosomal β‐galactosidase , 2006 .
[169] J. S. Pedersen,et al. The lncRNA MIR31HG regulates p16INK4A expression to modulate senescence , 2015, Nature Communications.
[170] C. Garbe,et al. Increase of melanocytic nevus counts in children during 5 years of follow-up and analysis of associated factors. , 1996, Archives of dermatology.
[171] R. Dummer,et al. The Genetic Evolution of Melanoma from Precursor Lesions. , 2015, The New England journal of medicine.
[172] W. Goggins,et al. The transformation rate of moles (melanocytic nevi) into cutaneous melanoma: a population-based estimate. , 2003, Archives of dermatology.
[173] J. Weber,et al. ARF tumor suppression in the nucleolus. , 2014, Biochimica et biophysica acta.
[174] Dimitris Kletsas,et al. Oncogene-induced senescence is part of the tumorigenesis barrier imposed by DNA damage checkpoints , 2006, Nature.
[175] S. Lowe,et al. Premature senescence involving p53 and p16 is activated in response to constitutive MEK/MAPK mitogenic signaling. , 1998, Genes & development.
[176] Michael R. Green,et al. Role for IGFBP7 in Senescence Induction by BRAF , 2010, Cell.
[177] Y. Moroi,et al. Expression of c-Kit, p-ERK and cyclin D1 in malignant melanoma: an immunohistochemical study and analysis of prognostic value. , 2011, Journal of dermatological science.
[178] R. Bergman,et al. Apoptosis, Fas and Fas‐ligand expression in melanocytic tumors , 1999, Journal of cutaneous pathology.
[179] F. Haluska,et al. Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma. , 2004, The Journal of investigative dermatology.
[180] T. Spector,et al. Nevus Size and Number Are Associated with Telomere Length and Represent Potential Markers of a Decreased Senescence In vivo , 2007, Cancer Epidemiology Biomarkers & Prevention.
[181] S. Keyse,et al. The regulation of oncogenic Ras/ERK signalling by dual-specificity mitogen activated protein kinase phosphatases (MKPs) , 2016, Seminars in cell & developmental biology.
[182] J. A. Bishop,et al. Genotype/phenotype and penetrance studies in melanoma families with germline CDKN2A mutations. , 2000, The Journal of investigative dermatology.
[183] M. Tronnier,et al. One single erythemagenic UV irradiation is more effective in increasing the proliferative activity of melanocytes in melanocytic naevi compared with fractionally applied high doses , 1997, The British journal of dermatology.
[184] C. Dang,et al. MYC, Metabolism, and Cancer. , 2015, Cancer discovery.
[185] R. Kitsis,et al. MacroH2A1 and ATM Play Opposing Roles in Paracrine Senescence and the Senescence-Associated Secretory Phenotype. , 2015, Molecular cell.
[186] M. Herlyn,et al. Targeting ER stress-induced autophagy overcomes BRAF inhibitor resistance in melanoma. , 2014, The Journal of clinical investigation.
[187] P. Sorensen,et al. IGFBP7 Binds to the IGF-1 Receptor and Blocks Its Activation by Insulin-Like Growth Factors , 2012, Science Signaling.
[188] Thomas M. Keane,et al. POT1 loss-of-function variants predispose to familial melanoma , 2014, Nature Genetics.
[189] D. Schadendorf,et al. TERT Promoter Mutations in Familial and Sporadic Melanoma , 2013, Science.
[190] G. Robertson,et al. Akt3 and mutant V600E B-Raf cooperate to promote early melanoma development. , 2008, Cancer research.
[191] C. Harley,et al. Telomeres shorten during ageing of human fibroblasts , 1990, Nature.
[192] A. Emley,et al. RAS and RAF mutations in banal melanocytic aggregates contiguous with primary cutaneous melanoma: clues to melanomagenesis , 2009, The British journal of dermatology.
[193] R. DePinho,et al. BRafV600E cooperates with Pten silencing to elicit metastatic melanoma , 2009, Nature Genetics.
[194] R. Stern,et al. Incidence of skin cancer in 5356 patients following organ transplantation , 2000, The British journal of dermatology.
[195] G. Mollica,et al. Are Melanocytic Nevi Influenced by Pregnancy? A Dermoscopic Evaluation , 2006, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].
[196] J. Slingerland,et al. Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma. , 1995, Oncogene.
[197] P. Dhawan,et al. Constitutive activation of Akt/protein kinase B in melanoma leads to up-regulation of nuclear factor-kappaB and tumor progression. , 2002, Cancer research.
[198] S. Menzies,et al. Variables predicting change in benign melanocytic nevi undergoing short-term dermoscopic imaging. , 2011, Archives of dermatology.
[199] C. Grin,et al. The immune response in halo nevi. , 1997, Journal of the American Academy of Dermatology.
[200] A. Elefanty,et al. Human acquired naevi are clonal , 1998, Melanoma research.
[201] A. Zwinderman,et al. Vitiligo-like depigmentation in patients with stage III-IV melanoma receiving immunotherapy and its association with survival: a systematic review and meta-analysis. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[202] C. Harley,et al. Extension of life-span by introduction of telomerase into normal human cells. , 1998, Science.
[203] J. Campisi,et al. Replicative Senescence: An Old Lives' Tale? , 1996, Cell.
[204] G. Annessi,et al. Correlation between clinical atypia and histologic dysplasia in acquired melanocytic nevi. , 2001, Journal of the American Academy of Dermatology.
[205] C. Garbe,et al. Acquired melanocytic nevi as risk factor for melanoma development. A comprehensive review of epidemiological data. , 2003, Pigment cell research.
[206] The developing story of Sprouty and cancer , 2014, Cancer and Metastasis Reviews.
[207] S. Mocellin,et al. Interferon alpha for the adjuvant treatment of cutaneous melanoma. , 2013, The Cochrane database of systematic reviews.
[208] C. Lengner,et al. DNA-damage-induced type I interferon promotes senescence and inhibits stem cell function. , 2015, Cell reports.
[209] M. Saroufim,et al. Predictors of BRAF Mutation in Melanocytic Nevi: Analysis Across Regions With Different UV Radiation Exposure , 2013, The American Journal of dermatopathology.
[210] S. Gruber,et al. Anti-oncogenic role of the endoplasmic reticulum differentially activated by mutations in the MAPK pathway , 2006, Nature Cell Biology.
[211] P. Uribe,et al. Lack of association between BRAF mutation and MAPK ERK activation in melanocytic nevi. , 2006, The Journal of investigative dermatology.
[212] P. Soares,et al. Overexpression of pyruvate dehydrogenase kinase supports dichloroacetate as a candidate for cutaneous melanoma therapy , 2015, Expert opinion on therapeutic targets.
[213] S. J. Lee,et al. Melanocytic nevus with pregnancy-related changes in size accompanied by apoptosis of nevus cells: a case report. , 2000, Journal of the American Academy of Dermatology.
[214] P. Mischel,et al. mTORC2 in the center of cancer metabolic reprogramming , 2014, Trends in Endocrinology & Metabolism.
[215] D. English,et al. Ultraviolet Radiation at Places of Residence and the Development of Melanocytic Nevi in Children (Australia) , 2006, Cancer Causes & Control.
[216] Thomas M. Keane,et al. Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. , 2015, Journal of the National Cancer Institute.
[217] D. Peeper,et al. BRAFE600 in benign and malignant human tumours , 2008, Oncogene.
[218] S. Arron,et al. Melanoma risk and survival among organ transplant recipients , 2015, The Journal of investigative dermatology.
[219] H. Kittler,et al. Frequency and characteristics of enlarging common melanocytic nevi. , 2000, Archives of Dermatology.
[220] P. A. Pérez-Mancera,et al. Inside and out: the activities of senescence in cancer , 2014, Nature Reviews Cancer.
[221] D. Sabatini,et al. mTOR Signaling in Growth Control and Disease , 2012, Cell.
[222] F. Trautinger,et al. Prevalence of actinic keratosis among dermatology outpatients in Austria , 2014, The British journal of dermatology.
[223] P. Guldberg,et al. Molecular drivers of cellular metabolic reprogramming in melanoma. , 2015, Trends in molecular medicine.
[224] Sikandar G. Khan,et al. High frequency of PTEN mutations in nevi and melanomas from xeroderma pigmentosum patients , 2014, Pigment cell & melanoma research.
[225] S. Tahan,et al. Melanocytic nevi in pregnancy: histologic features and Ki‐67 proliferation index , 2009, Journal of cutaneous pathology.
[226] Peter D. Adams,et al. Lysosome-mediated processing of chromatin in senescence , 2013, The Journal of cell biology.
[227] J. Fridlyand,et al. Distinct sets of genetic alterations in melanoma. , 2005, The New England journal of medicine.
[228] Dritan Liko,et al. mTOR in health and in sickness , 2015, Journal of Molecular Medicine.
[229] A. Perkins,et al. Assessment of clonality in melanocytic nevi , 2001, Journal of cutaneous pathology.
[230] S. Puig,et al. Nevus-associated melanomas: clinicopathologic features. , 2014, American journal of clinical pathology.
[231] D. Sabatini,et al. Cancer cell metabolism: one hallmark, many faces. , 2012, Cancer discovery.
[232] A. Enk,et al. RASSF10 promoter hypermethylation is frequent in malignant melanoma of the skin but uncommon in nevus cell nevi. , 2012, The Journal of investigative dermatology.
[233] P. Ascierto,et al. Melanoma: From Incurable Beast to a Curable Bet. The Success of Immunotherapy , 2015, Front. Oncol..
[234] J. Cerhan,et al. Increased incidence of malignant melanoma and other rare cutaneous cancers in the setting of chronic lymphocytic leukemia , 2015, International journal of dermatology.
[235] J. Bouwes Bavinck,et al. Melanoma in Organ Transplant Recipients: Clinicopathological Features and Outcome in 100 Cases , 2008, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[236] P. Vogt,et al. Attenuation of TORC1 signaling delays replicative and oncogenic RAS-induced senescence , 2012, Cell cycle.
[237] M. Skolnick,et al. Inheritance of nevus number and size in melanoma and dysplastic nevus syndrome kindreds. , 1991, Journal of the National Cancer Institute.
[238] E. Yang,et al. The intersection between DNA damage response and cell death pathways. , 2012, Experimental oncology.
[239] N. Carter,et al. A DNA damage checkpoint response in telomere-initiated senescence , 2003, Nature.
[240] S. Haferkamp,et al. Absence of distinguishing senescence traits in human melanocytic nevi. , 2012, The Journal of investigative dermatology.
[241] M. Mihm,et al. Recurrent nevus phenomenon: a clinicopathologic study of 357 cases and histologic comparison with melanoma with regression , 2009, Modern Pathology.
[242] R. Curran,et al. The ultrastructure of benign pigmented naevi and melanocarcinomas in man , 1976, The Journal of pathology.
[243] L. Zon,et al. BRAF Mutations Are Sufficient to Promote Nevi Formation and Cooperate with p53 in the Genesis of Melanoma , 2005, Current Biology.
[244] David T. W. Jones,et al. Signatures of mutational processes in human cancer , 2013, Nature.
[245] Alexander Roesch,et al. A Temporarily Distinct Subpopulation of Slow-Cycling Melanoma Cells Is Required for Continuous Tumor Growth , 2010, Cell.
[246] J. Kirkwood,et al. Association of TERT promoter mutations with telomerase expression in melanoma , 2016, Pigment cell & melanoma research.
[247] E. Simpson,et al. p53: Protection against Tumor Growth beyond Effects on Cell Cycle and Apoptosis. , 2015, Cancer research.
[248] P. Helmbold,et al. Claudin11 Promoter Hypermethylation Is Frequent in Malignant Melanoma of the Skin, but Uncommon in Nevus Cell Nevi , 2015, Cancers.
[249] D. DiMaio,et al. Senescence-associated beta-galactosidase is lysosomal beta-galactosidase. , 2006, Aging cell.
[250] P. Romero,et al. C O M M E N T a R Y Open Access , 2022 .
[251] S. Pathak,et al. Spontaneous regression of cutaneous melanoma in sinclair swine is associated with defective telomerase activity and extensive telomere erosion. , 2000, International journal of oncology.
[252] D. Morton,et al. Immunological factors which influence response to immunotherapy in malignant melanoma. , 1970, Surgery.
[253] R. Sears,et al. Diminished WNT → β-catenin → c-MYC signaling is a barrier for malignant progression of BRAFV600E-induced lung tumors , 2014, Genes & development.
[254] H. Horlings,et al. Abrogation of BRAFV600E-induced senescence by PI3K pathway activation contributes to melanomagenesis. , 2012, Genes & development.
[255] D. Rimm,et al. β-catenin signaling controls metastasis in Braf-activated Pten-deficient melanomas. , 2011, Cancer cell.
[256] G. Feldman,et al. The macrophage: Switches from a passenger to a driver during anticancer therapy , 2015, Oncoimmunology.
[257] P. Puigserver,et al. Cyclin D1-CDK4 Controls Glucose Metabolism Independently of Cell Cycle Progression , 2014, Nature.
[258] W. Clark,et al. Growth and phenotypic characteristics of human nevus cells in culture. , 1988, The Journal of investigative dermatology.
[259] J. Malvehy,et al. Mutational status of naevus‐associated melanomas , 2015, The British journal of dermatology.
[260] J. J. van den Oord,et al. Analysis of N- and K-ras mutations in the distinctive tumor progression phases of melanoma. , 2001, The Journal of investigative dermatology.
[261] W. Goggins,et al. Cutaneous melanomas associated with nevi. , 2003, Archives of dermatology.
[262] N. Hayward,et al. Nuclear PTEN expression and clinicopathologic features in a population‐based series of primary cutaneous melanoma , 2002, International journal of cancer.
[263] M. Mihm,et al. Histologic regression in malignant melanoma: an interobserver concordance study , 1993, Journal of cutaneous pathology.
[264] K. Drzewiecki,et al. Spontaneous regression of metastases from melanoma: review of the literature , 2009, Melanoma research.
[265] J. Metcalf,et al. Blue nevus and "malignant blue nevus:" A concise review. , 2016, Seminars in diagnostic pathology.
[266] C. Abbadie,et al. The unfolded protein response and cellular senescence. A review in the theme: cellular mechanisms of endoplasmic reticulum stress signaling in health and disease. , 2015, American journal of physiology. Cell physiology.
[267] J. Goeman,et al. Promoter CpG island hypermethylation in dysplastic nevus and melanoma: CLDN11 as an epigenetic biomarker for malignancy. , 2014, The Journal of investigative dermatology.
[268] M. Esteller,et al. Aberrant epigenetic landscape in cancer: how cellular identity goes awry. , 2010, Developmental cell.
[269] R. Mohney,et al. Oncogene-induced senescence results in marked metabolic and bioenergetic alterations , 2012, Cell cycle.
[270] P. Aronson,et al. Sorafenib induced eruptive melanocytic lesions. , 2013, Dermatology online journal.
[271] Aaron Bensimon,et al. Oncogene-induced senescence is a DNA damage response triggered by DNA hyper-replication , 2006, Nature.
[272] D. Elder,et al. TIA-1 Positive Tumor-Infiltrating Lymphocytes in Nevi and Melanomas , 2000, Modern Pathology.
[273] A. Lund,et al. Emerging roles of lncRNAs in senescence , 2016, The FEBS journal.
[274] R. Sagebiel,et al. Melanocytic nevi in histologic association with primary cutaneous melanoma of superficial spreading and nodular types: effect of tumor thickness. , 1993, The Journal of investigative dermatology.
[275] W. Stolz,et al. Increase in telomerase activity during progression of melanocytic cells from melanocytic naevi to malignant melanomas , 1999, Archives of Dermatological Research.
[276] Clara Correia-Melo,et al. Telomeres are favoured targets of a persistent DNA damage response in ageing and stress-induced senescence , 2012, Nature Communications.
[277] Y. Collan,et al. Loss of expression of the p16INK4/CDKN2 gene in cutaneous malignant melanoma correlates with tumor cell proliferation and invasive stage , 1997, International journal of cancer.
[278] Raymond L. Barnhill,et al. Pathology of melanocytic nevi and melanoma , 2014 .
[279] H. Kutzner,et al. Frequent Mitotic Activity in Banal Melanocytic Nevi Uncovered by Immunohistochemical Analysis , 2010, The American Journal of dermatopathology.
[280] N. Bardeesy,et al. mTORC1 activation blocks BrafV600E-induced growth arrest but is insufficient for melanoma formation. , 2015, Cancer cell.
[281] M. Mihm,et al. Dysplastic melanocytic nevi in histologic association with 234 primary cutaneous melanomas. , 1983, Journal of the American Academy of Dermatology.
[282] R. Taub,et al. B.C.G. in malignant melanoma. , 1973, The Lancet.
[283] S. Lowe,et al. Oncogenic ras Provokes Premature Cell Senescence Associated with Accumulation of p53 and p16INK4a , 1997, Cell.
[284] M. Skolnick,et al. Histopathologic characteristics of dysplastic nevi. Limited association of conventional histologic criteria with melanoma risk group. , 1990, Journal of the American Academy of Dermatology.
[285] K. Isselbacher,et al. Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[286] Dimitris Kletsas,et al. Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions , 2005, Nature.
[287] Y. Shyr,et al. Expression of activated Akt in benign nevi, Spitz nevi and melanomas , 2007, Journal of cutaneous pathology.
[288] T. Shlomi,et al. A key role for mitochondrial gatekeeper pyruvate dehydrogenase in oncogene-induced senescence , 2013, Nature.
[289] K. Brown,et al. Germline TERT promoter mutations are rare in familial melanoma , 2015, Familial Cancer.
[290] C. Eng,et al. Epigenetic PTEN silencing in malignant melanomas without PTEN mutation. , 2000, The American journal of pathology.
[291] Michael P Schön,et al. Association of Patient Risk Factors and Frequency of Nevus-Associated Cutaneous Melanomas. , 2016, JAMA dermatology.
[292] F. D. D. Fagagna,et al. Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation , 2012, Nature Cell Biology.
[293] L. Zender,et al. mTOR regulates MAPKAPK2 translation to control the senescence-associated secretory phenotype , 2015, Nature Cell Biology.
[294] M. Fimiani,et al. Quantitative in situ evaluation of telomeres in fluorescence in situ hybridization‐processed sections of cutaneous melanocytic lesions and correlation with telomerase activity , 2002, The British journal of dermatology.
[295] B. Kerem,et al. Nucleotide Deficiency Promotes Genomic Instability in Early Stages of Cancer Development , 2011, Cell.
[296] M. Mihm,et al. PTEN expression in normal skin, acquired melanocytic nevi, and cutaneous melanoma. , 2003, Journal of the American Academy of Dermatology.
[297] M. Saroufim,et al. BRAF Analysis on a Spectrum of Melanocytic Neoplasms: An Epidemiological Study Across Differing UV Regions , 2014, The American Journal of dermatopathology.
[298] H. Soyer,et al. BRAF wild-type melanoma in situ arising in a BRAF V600E mutant dysplastic nevus. , 2015, JAMA dermatology.
[299] Sebastian Moran,et al. Epigenetic mechanisms involved in melanoma pathogenesis and chemoresistance. , 2015, Annals of translational medicine.
[300] R. Newbold,et al. Fibroblast immortality is a prerequisite for transformation by EJ c-Ha-ras oncogene , 1983, Nature.
[301] D. Rimm,et al. Frequent nuclear/cytoplasmic localization of beta-catenin without exon 3 mutations in malignant melanoma. , 1999, The American journal of pathology.
[302] William M. Lin,et al. Outcome of patients with de novo versus nevus-associated melanoma. , 2015, Journal of the American Academy of Dermatology.
[303] R. Brodell,et al. The natural history of halo nevi: a retrospective case series. , 2012, Journal of the American Academy of Dermatology.
[304] M. Arumí-Uría,et al. Grading of Atypia in Nevi: Correlation with Melanoma Risk , 2003, Modern Pathology.
[305] I. Zalaudek,et al. Spitz nevus, Spitz tumor, and spitzoid melanoma: a comprehensive clinicopathologic overview. , 2013, Dermatologia clinica.
[306] A. Mantovani,et al. Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft. , 2007, The Journal of investigative dermatology.
[307] E. Papakonstanti,et al. Focus on PTEN Regulation , 2015, Front. Oncol..
[308] J. Shay,et al. Progressive increase in telomerase activity from benign melanocytic conditions to malignant melanoma. , 1999, Neoplasia.
[309] N. Hayward,et al. Genetics of familial melanoma: 20 years after CDKN2A , 2015, Pigment cell & melanoma research.
[310] Douglas Hanahan,et al. Accessories to the Crime: Functions of Cells Recruited to the Tumor Microenvironment Prospects and Obstacles for Therapeutic Targeting of Function-enabling Stromal Cell Types , 2022 .
[311] S. Florell,et al. Proliferation, apoptosis, and survivin expression in a spectrum of melanocytic nevi , 2005, Journal of cutaneous pathology.
[312] K. Flaherty,et al. Promoter Methylation of PTEN Is a Significant Prognostic Factor in Melanoma Survival. , 2016, The Journal of investigative dermatology.
[313] C. Burd,et al. The Molecular Balancing Act of p16INK4a in Cancer and Aging , 2013, Molecular Cancer Research.
[314] H. Kerl,et al. Melanoma ex naevo: a study of the associated naevus , 2003, Melanoma research.
[315] M. Bosenberg,et al. Melanoma metastasis: new concepts and evolving paradigms , 2014, Oncogene.
[316] R. Scolyer,et al. Expression of glucose‐regulated stress protein GRP78 is related to progression of melanoma , 2009, Histopathology.
[317] D. Pinkel,et al. Mutations and copy number increase of HRAS in Spitz nevi with distinctive histopathological features. , 2000, The American journal of pathology.
[318] M. Tetzlaff,et al. Loss of microRNA-205 expression is associated with melanoma progression , 2012, Laboratory Investigation.
[319] C. Shea,et al. The recurrent nevus phenomenon: a history of challenge, controversy, and discovery. , 2011, Archives of pathology & laboratory medicine.
[320] M. Bergo,et al. Oncogene-induced senescence underlies the mutual exclusive nature of oncogenic KRAS and BRAF , 2016, Oncogene.
[321] Bonnie L. Balzer,et al. Nevic Mitoses: A Review of 1041 Cases , 2013, The American Journal of dermatopathology.
[322] L. Cantley,et al. Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation , 2009, Science.
[323] J. Magaud,et al. Association of increased autophagic inclusions labeled for β-galactosidase with fibroblastic aging , 2003, Experimental Gerontology.
[324] M. Askarian-Amiri,et al. Epigenetic regulation in human melanoma: past and future , 2015, Epigenetics.
[325] Brian Keith,et al. HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression , 2011, Nature Reviews Cancer.
[326] N. Dhomen,et al. Ultraviolet radiation accelerates BRAF-driven melanomagenesis by targeting TP53 , 2014, Nature.
[327] R. Newbold,et al. Induction of immortality is an early event in malignant transformation of mammalian cells by carcinogens , 1982, Nature.
[328] Amy Y. M. Au,et al. p53 status determines the role of autophagy in pancreatic tumour development , 2013, Nature.
[329] W. Clark,et al. Biology of tumor progression in human melanocytes. , 1987, Laboratory investigation; a journal of technical methods and pathology.
[330] Michael R. Green,et al. Oncogenic BRAF Induces Senescence and Apoptosis through Pathways Mediated by the Secreted Protein IGFBP7 , 2008, Cell.
[331] A. Nicholson,et al. Mutations of the BRAF gene in human cancer , 2002, Nature.