Mutant p53: one name, many proteins.
暂无分享,去创建一个
[1] W. Deppert,et al. The complex interactions of p53 with target DNA: we learn as we go. , 2003, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[2] E. Feinstein,et al. Small-molecule RETRA suppresses mutant p53-bearing cancer cells through a p73-dependent salvage pathway , 2008, Proceedings of the National Academy of Sciences.
[3] L. Strong,et al. Gain of Function of a p53 Hot Spot Mutation in a Mouse Model of Li-Fraumeni Syndrome , 2004, Cell.
[4] P. Schirmacher,et al. Protumorigenic overexpression of stathmin/Op18 by gain‐of‐function mutation in p53 in human hepatocarcinogenesis , 2007, Hepatology.
[5] J. Fraumeni,et al. Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome. , 1969, Journal of the National Cancer Institute.
[6] Joost Schymkowitz,et al. Gain of function of mutant p53 by coaggregation with multiple tumor suppressors. , 2011, Nature chemical biology.
[7] S. Sykes,et al. The p53 family and programmed cell death , 2008, Oncogene.
[8] L. Strong,et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. , 1990, Science.
[9] J. Momand,et al. Heat Shock Protein 84 Forms a Complex with Mutant p53 Protein Predominantly within a Cytoplasmic Compartment of the Cell* , 1996, The Journal of Biological Chemistry.
[10] Xinbin Chen,et al. Identification of a Novel p53 Functional Domain That Is Necessary for Mediating Apoptosis* , 1998, The Journal of Biological Chemistry.
[11] M. Olivier,et al. Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database , 2007, Human mutation.
[12] David Lane,et al. p53 Research: the past thirty years and the next thirty years. , 2010, Cold Spring Harbor perspectives in biology.
[13] A. Levine,et al. Several hydrophobic amino acids in the p53 amino-terminal domain are required for transcriptional activation, binding to mdm-2 and the adenovirus 5 E1B 55-kD protein. , 1994, Genes & development.
[14] C. Stratakis,et al. An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[15] V. Rotter,et al. Integrity of the N‐terminal transcription domain of p53 is required for mutant p53 interference with drug‐induced apoptosis , 2001, The EMBO journal.
[16] T. Iwakuma,et al. The inherent instability of mutant p53 is alleviated by Mdm2 or p16INK4a loss. , 2008, Genes & development.
[17] E. Sugikawa,et al. Mutant p53 mediated induction of cell cycle arrest and apoptosis at G1 phase by 9-hydroxyellipticine. , 1999, Anticancer research.
[18] E. Franco,et al. Persistent human papillomavirus infection and cervical neoplasia. , 2002, The Lancet. Oncology.
[19] J. Bourdon,et al. p53 family members in cancer diagnosis and treatment. , 2010, Seminars in cancer biology.
[20] J. Shay,et al. A transcriptionally active DNA-binding site for human p53 protein complexes , 1992, Molecular and cellular biology.
[21] Galina Selivanova,et al. Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound , 2002, Nature Medicine.
[22] M. Hsiao,et al. Gain-of-function mutations of the p53 gene induce lymphohematopoietic metastatic potential and tissue invasiveness. , 1994, The American journal of pathology.
[23] Hongjuan Zhao,et al. TP53 mutation status and gene expression profiles are powerful prognostic markers of breast cancer , 2007, Breast Cancer Research.
[24] F. Talos,et al. Functional Inactivation of Endogenous MDM2 and CHIP by HSP90 Causes Aberrant Stabilization of Mutant p53 in Human Cancer Cells , 2011, Molecular Cancer Research.
[25] P. Gruss,et al. Participation of p53 cellular tumour antigen in transformation of normal embryonic cells , 1984, Nature.
[26] J. Norman,et al. Mutant p53 Drives Invasion by Promoting Integrin Recycling , 2009, Cell.
[27] Jiandong Chen,et al. Inhibition of MDM2 by hsp90 Contributes to Mutant p53 Stabilization* , 2001, The Journal of Biological Chemistry.
[28] T. Soussi,et al. p53 mutation heterogeneity in cancer. , 2005, Biochemical and biophysical research communications.
[29] S. Berger,et al. Two tandem and independent sub-activation domains in the amino terminus of p53 require the adaptor complex for activity , 1997, Oncogene.
[30] E. Silbergeld,et al. P53 mutations associated with breast, colorectal, liver, lung, and ovarian cancers. , 1996, Environmental health perspectives.
[31] A. El‐Naggar,et al. Multiple stress signals activate mutant p53 in vivo. , 2011, Cancer research.
[32] B. Strauss,et al. The region 3' to the major transcriptional start site of the MDR1 downstream promoter mediates activation by a subset of mutant P53 proteins. , 1995, Biochemical and biophysical research communications.
[33] E. Appella,et al. Detection of a transformation-related antigen in chemically induced sarcomas and other transformed cells of the mouse. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[34] N. Basset-Seguin,et al. TP53 tumor suppressor gene and skin carcinogenesis. , 1994, The Journal of investigative dermatology.
[35] V. Rotter,et al. Cooperation between gene encoding p53 tumour antigen and ras in cellular transformation , 1984, Nature.
[36] C. Prives,et al. Blinded by the Light: The Growing Complexity of p53 , 2009, Cell.
[37] K. Kinzler,et al. Definition of a consensus binding site for p53 , 1992, Nature Genetics.
[38] G. Wahl,et al. Inactivation of p53 in breast cancers correlates with stem cell transcriptional signatures , 2010, Proceedings of the National Academy of Sciences.
[39] S. Deb,et al. Transcriptional activation of the human epidermal growth factor receptor promoter by human p53 , 1996, Molecular and cellular biology.
[40] M. Tada,et al. Mutant p53 R248Q but not R248W enhances in vitro invasiveness of human lung cancer NCI-H1299 cells. , 2010, Biomedical research.
[41] V. Rotter,et al. Understanding wild-type and mutant p53 activities in human cancer: new landmarks on the way to targeted therapies , 2011, Cancer Gene Therapy.
[42] Thierry Soussi,et al. TP53 tumor suppressor gene: A model for investigating human mutagenesis , 1992, Genes, chromosomes & cancer.
[43] W. Hahn,et al. Chemosensitivity linked to p73 function. , 2003, Cancer cell.
[44] H. Werner,et al. Wild-type and mutant p53 differentially regulate transcription of the insulin-like growth factor I receptor gene. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[45] G. Blandino,et al. Mutant p53 gain of function: reduction of tumor malignancy of human cancer cell lines through abrogation of mutant p53 expression , 2006, Oncogene.
[46] B. Gusterson,et al. A common polymorphism acts as an intragenic modifier of mutant p53 behaviour , 2000, Nature Genetics.
[47] Erwin G. Van Meir,et al. Tumor suppressor p53 inhibits transcriptional activation of invasion gene thromboxane synthase mediated by the proto-oncogenic factor ets-1 , 2003, Oncogene.
[48] Y. Sung,et al. Transactivation Ability of p53 Transcriptional Activation Domain Is Directly Related to the Binding Affinity to TATA-binding Protein (*) , 1995, The Journal of Biological Chemistry.
[49] A. Torgeman,et al. Sp1-p53 heterocomplex mediates activation of HTLV-I long terminal repeat by 12-O-tetradecanoylphorbol-13-acetate that is antagonized by protein kinase C. , 2001, Virology.
[50] M. Kapoor,et al. High metastatic potential in mice inheriting a targeted p53 missense mutation. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[51] Daxi Sun,et al. Mutant p53 Cooperates with ETS and Selectively Up-regulates Human MDR1 Not MRP1* , 2001, The Journal of Biological Chemistry.
[52] G. Wahl,et al. Keeping p53 in check: essential and synergistic functions of Mdm2 and Mdm4 , 2006, Cell Death and Differentiation.
[53] K. Aldape,et al. An oncogenic form of p53 confers a dominant, gain-of-function phenotype that disrupts spindle checkpoint control. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[54] I. Simon,et al. Modulation of the vitamin D3 response by cancer-associated mutant p53. , 2010, Cancer cell.
[55] Y. Zhang,et al. Reactivation of p53 by inhibiting Mdm2 E3 ligase: a novel antitumor approach. , 2011, Current cancer drug targets.
[56] D. Medina,et al. Expression of a p53 mutant in the epidermis of transgenic mice accelerates chemical carcinogenesis , 1998, Oncogene.
[57] C. Prives,et al. p73 Function Is Inhibited by Tumor-Derived p53 Mutants in Mammalian Cells , 1999, Molecular and Cellular Biology.
[58] A. Yang,et al. Tumor predisposition in mice mutant for p63 and p73: evidence for broader tumor suppressor functions for the p53 family. , 2005, Cancer cell.
[59] A. Børresen-Dale,et al. A comparison between p53 accumulation determined by immunohistochemistry and TP53 mutations as prognostic variables in tumours from breast cancer patients , 2008, Acta oncologica.
[60] C. Prives,et al. Are interactions with p63 and p73 involved in mutant p53 gain of oncogenic function? , 2007, Oncogene.
[61] V. Rotter,et al. Conditional RNA interference in vivo to study mutant p53 oncogenic gain of function on tumor malignancy , 2008, Cell cycle.
[62] A. Levine,et al. Identification of a novel p53 functional domain that is necessary for efficient growth suppression. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[63] Antonio Rosato,et al. A Pin1/mutant p53 axis promotes aggressiveness in breast cancer. , 2011, Cancer cell.
[64] A. Levine,et al. The first 30 years of p53: growing ever more complex , 2009, Nature Reviews Cancer.
[65] D. Hanahan,et al. Hallmarks of Cancer: The Next Generation , 2011, Cell.
[66] G. Blandino,et al. Mutant p53: an oncogenic transcription factor , 2007, Oncogene.
[67] R. Poon,et al. How Many Mutant p53 Molecules Are Needed To Inactivate a Tetramer? , 2004, Molecular and Cellular Biology.
[68] A. Fersht,et al. Four domains of p300 each bind tightly to a sequence spanning both transactivation subdomains of p53 , 2007, Proceedings of the National Academy of Sciences.
[69] R. Altman,et al. Wild Type and Mutant p53 Differentially Regulate the Gene Expression of Human Collagenase-3 (hMMP-13)* , 2000, The Journal of Biological Chemistry.
[70] V. Rotter,et al. Mutant p53 enhances nuclear factor kappaB activation by tumor necrosis factor alpha in cancer cells. , 2007, Cancer research.
[71] U. Moll,et al. SAHA shows preferential cytotoxicity in mutant p53 cancer cells by destabilizing mutant p53 through inhibition of the HDAC6-Hsp90 chaperone axis , 2011, Cell Death and Differentiation.
[72] W. McGuire,et al. Prognostic significance of p53 gene alterations in node-negative breast cancer , 2004, Breast Cancer Research and Treatment.
[73] J. Marine,et al. Mdm2-mediated ubiquitylation: p53 and beyond , 2010, Cell Death and Differentiation.
[74] W. Deppert,et al. Transcriptional activities of mutant p53: When mutations are more than a loss , 2004, Journal of cellular biochemistry.
[75] C. Prives,et al. Transcriptional regulation by p53: one protein, many possibilities , 2006, Cell Death and Differentiation.
[76] M. Oren,et al. Specific loss of apoptotic but not cell‐cycle arrest function in a human tumor derived p53 mutant. , 1996, The EMBO journal.
[77] A. El‐Naggar,et al. Restoring expression of wild-type p53 suppresses tumor growth but does not cause tumor regression in mice with a p53 missense mutation. , 2011, The Journal of clinical investigation.
[78] Varda Rotter,et al. When mutants gain new powers: news from the mutant p53 field , 2009, Nature Reviews Cancer.
[79] Carlos Cordon-Cardo,et al. Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas , 2007, Nature.
[80] R. Weinberg. Tumor suppressor genes , 1993, Neuron.
[81] T. Davison,et al. p73 and p63 Are Homotetramers Capable of Weak Heterotypic Interactions with Each Other but Not with p53* , 1999, The Journal of Biological Chemistry.
[82] T. Soussi,et al. Change of Conformation of the DNA-binding Domain of p53 Is the Only Key Element for Binding of and Interference with p73* , 2003, The Journal of Biological Chemistry.
[83] V. Rotter,et al. Inactivation of p53 gene expression by an insertion of Moloney murine leukemia virus-like DNA sequences , 1984, Molecular and cellular biology.
[84] Antonio Rosato,et al. A Mutant-p53/Smad Complex Opposes p63 to Empower TGFβ-Induced Metastasis , 2009, Cell.
[85] V. Rotter,et al. Transactivation of the EGR1 Gene Contributes to Mutant p53 Gain of Function , 2004, Cancer Research.
[86] Lawrence A. Donehower,et al. 20 years studying p53 functions in genetically engineered mice , 2009, Nature Reviews Cancer.
[87] Sook Y. Lee,et al. Activation of the insulin-like growth factor II transcription by aflatoxin B1 induced p53 mutant 249 is caused by activation of transcription complexes; implications for a gain-of-function during the formation of hepatocellular carcinoma , 2000, Oncogene.
[88] A. Levine,et al. The Spectrum of Mutations at the p53 Locus , 1995, Annals of the New York Academy of Sciences.
[89] Wafik S El-Deiry,et al. Current strategies to target p53 in cancer. , 2010, Biochemical pharmacology.
[90] V. Rotter,et al. p53 Regulates the Ras circuit to inhibit the expression of a cancer-related gene signature by various molecular pathways. , 2010, Cancer research.
[91] L. Wiesmüller,et al. Specific interaction of mutant p53 with regions of matrix attachment region DNA elements (MARs) with a high potential for base-unpairing. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[92] W. Deppert,et al. Modulation of gene expression in U251 glioblastoma cells by binding of mutant p53 R273H to intronic and intergenic sequences , 2009, Nucleic acids research.
[93] B. Vogelstein,et al. Mutant p53 DNA clones from human colon carcinomas cooperate with ras in transforming primary rat cells: a comparison of the "hot spot" mutant phenotypes. , 1990, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[94] T. Jacks,et al. Mutant p53 Gain of Function in Two Mouse Models of Li-Fraumeni Syndrome , 2004, Cell.
[95] A. Levine. The common mechanisms of transformation by the small DNA tumor viruses: The inactivation of tumor suppressor gene products: p53. , 2009, Virology.
[96] G. Blandino,et al. Promyelocytic leukemia protein is required for gain of function by mutant p53. , 2009, Cancer research.
[97] A. Albor,et al. Induction of gene amplification as a gain-of-function phenotype of mutant p53 proteins. , 2002, Cancer research.
[98] M. Hollstein,et al. Clinical implications of the p53 tumor-suppressor gene. , 1993, The New England journal of medicine.
[99] W. Deppert,et al. Specific binding of MAR/SAR DNA-elements by mutant p53. , 1996, Oncogene.
[100] K. Wiman,et al. Pharmacological reactivation of mutant p53: from protein structure to the cancer patient , 2010, Oncogene.
[101] A. Fersht,et al. A peptide that binds and stabilizes p53 core domain: Chaperone strategy for rescue of oncogenic mutants , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[102] G. Bossi,et al. Mutant p53-induced Up-regulation of Mitogen-activated Protein Kinase Kinase 3 Contributes to Gain of Function* , 2010, The Journal of Biological Chemistry.
[103] V. Rotter,et al. Mutant p53 gain-of-function in cancer. , 2010, Cold Spring Harbor perspectives in biology.
[104] M. Minden,et al. HMG-CoA reductase inhibitors and the malignant cell: the statin family of drugs as triggers of tumor-specific apoptosis , 2002, Leukemia.
[105] D. Lane,et al. T antigen is bound to a host protein in SY40-transformed cells , 1979, Nature.
[106] W. Deppert,et al. Wild-type p53 in cancer cells: when a guardian turns into a blackguard. , 2009, Biochemical pharmacology.
[107] W. Kaelin,et al. Role of the newer p53 family proteins in malignancy , 2001, Apoptosis.
[108] J. Manfredi. The Mdm2-p53 relationship evolves: Mdm2 swings both ways as an oncogene and a tumor suppressor. , 2010, Genes & development.
[109] Ting Wang,et al. A global suppressor motif for p53 cancer mutants. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[110] X. Wang,et al. TP53 and liver carcinogenesis , 2003, Human mutation.
[111] R. Bristow,et al. Resistance to DNA-damaging agents is discordant from experimental metastatic capacity in MEF ras-transformants-expressing gain of function MTp53 , 2003, Oncogene.
[112] B. Groner,et al. Restoration of the growth suppression function of mutant p53 by a synthetic peptide derived from the p53 C-terminal domain , 1997, Nature Medicine.
[113] U. Preuss,et al. Tumor‐derived p53 mutant C174Y is a gain‐of‐function mutant which activates the fos promoter and enhances colony formation , 2000, International journal of cancer.
[114] A. Inga,et al. Functional mutants of the sequence-specific transcription factor p53 and implications for master genes of diversity , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[115] E. Domany,et al. The execution of the transcriptional axis mutant p53, E2F1 and ID4 promotes tumor neo-angiogenesis , 2009, Nature Structural &Molecular Biology.
[116] W. Deppert,et al. Identification of genomic DNA sequences bound by mutant p53 protein (Gly245→Ser) in vivo , 2000, Oncogene.
[117] W. Blattner,et al. Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndrome , 1990, Nature.
[118] Wensheng Yan,et al. Identification of GRO1 as a Critical Determinant for Mutant p53 Gain of Function* , 2009, Journal of Biological Chemistry.
[119] A. Levine,et al. Structure of the MDM2 Oncoprotein Bound to the p53 Tumor Suppressor Transactivation Domain , 1996, Science.
[120] A. Levine,et al. The p53 proto-oncogene can act as a suppressor of transformation , 1989, Cell.
[121] P. Graves,et al. p53 mutants induce transcription of NF-κB2 in H1299 cells through CBP and STAT binding on the NF-κB2 promoter and gain of function activity. , 2012, Archives of biochemistry and biophysics.
[122] C. Prives,et al. A Subset of Tumor-Derived Mutant Forms of p53 Down-Regulate p63 and p73 through a Direct Interaction with the p53 Core Domain , 2001, Molecular and Cellular Biology.
[123] A. Levine,et al. Mutant p53 Disrupts Mammary Tissue Architecture via the Mevalonate Pathway , 2012, Cell.
[124] S. Thorgeirsson,et al. Wild-type p53 controls cell motility and invasion by dual regulation of MET expression , 2011, Proceedings of the National Academy of Sciences.
[125] J. Fraumeni,et al. Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome? , 1969, Annals of internal medicine.
[126] R. Mantovani,et al. Direct p53 Transcriptional Repression: In Vivo Analysis of CCAAT-Containing G2/M Promoters , 2005, Molecular and Cellular Biology.
[127] V. Rotter,et al. Structural basis of restoring sequence-specific DNA binding and transactivation to mutant p53 by suppressor mutations. , 2009, Journal of molecular biology.
[128] Tomas Lindahl,et al. Repair and genetic consequences of endogenous DNA base damage in mammalian cells. , 2004, Annual review of genetics.
[129] E. Conseiller,et al. Definition of a p53 transactivation function-deficient mutant and characterization of two independent p53 transactivation subdomains , 1999, Oncogene.
[130] L. Attardi,et al. In vivo analysis of p53 tumor suppressor function using genetically engineered mouse models. , 2010, Carcinogenesis.
[131] M. Eisenstein,et al. The disruption of the protein complex mutantp53/p73 increases selectively the response of tumor cells to anticancer drugs , 2008, Cell cycle.
[132] M. Hollstein,et al. p53 gain-of-function cancer mutants induce genetic instability by inactivating ATM , 2007, Nature Cell Biology.
[133] K. Jeang,et al. Expression of mitotic spindle checkpoint protein hsMAD1 correlates with cellular proliferation and is activated by a gain-of-function p53 mutant. , 2002, Cancer research.
[134] V. Rotter,et al. Mutant p53 facilitates somatic cell reprogramming and augments the malignant potential of reprogrammed cells , 2010, The Journal of experimental medicine.
[135] Giulia Piaggio,et al. Gain of function of mutant p53: the mutant p53/NF-Y protein complex reveals an aberrant transcriptional mechanism of cell cycle regulation. , 2006, Cancer cell.
[136] C. Prives,et al. Mutant p53 gain of function: the NF-Y connection. , 2006, Cancer Cell.
[137] K. Khanna,et al. Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11 , 2012, Oncogene.
[138] Shiyun Ling,et al. TopBP1 Mediates Mutant p53 Gain of Function through NF-Y and p63/p73 , 2011, Molecular and Cellular Biology.
[139] C. Prives,et al. Unleashing the power of p53: lessons from mice and men. , 2006, Genes & development.
[140] L. Castagnoli,et al. Physical Interaction with Yes-associated Protein Enhances p73 Transcriptional Activity* , 2001, The Journal of Biological Chemistry.
[141] Toshihide Tsuda,et al. The TP53 gene, tobacco exposure, and lung cancer , 2003, Human mutation.
[142] M. Hollstein,et al. Knock-in mice with a chimeric human/murine p53 gene develop normally and show wild-type p53 responses to DNA damaging agents: a new biomedical research tool , 2001, Oncogene.
[143] Kevin M. Ryan,et al. p53 and metabolism , 2009, Nature Reviews Cancer.
[144] Upregulation of the mitochondrial transport protein, Tim50, by mutant p53 contributes to cell growth and chemoresistance. , 2011, Archives of biochemistry and biophysics.
[145] C. Prives,et al. The C-terminus of p53: the more you learn the less you know , 2001, Nature Structural Biology.
[146] V. Rotter,et al. Reconstitution of p53 expression in a nonproducer Ab-MuLV-transformed cell line by transfection of a functional p53 gene , 1984, Cell.
[147] M. Oren,et al. Physical Interaction with Human Tumor-derived p53 Mutants Inhibits p63 Activities* , 2002, The Journal of Biological Chemistry.
[148] A. Levine,et al. Mutant p53 gain of function: differential effects of different p53 mutants on resistance of cultured cells to chemotherapy , 1999, Oncogene.
[149] L. Donehower,et al. Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours , 1992, Nature.
[150] V. Rotter,et al. Oncogenic mutations of the p53 tumor suppressor: the demons of the guardian of the genome. , 2000, Cancer research.
[151] A. Jochemsen,et al. MDMX: a novel p53‐binding protein with some functional properties of MDM2. , 1996, The EMBO journal.
[152] I. Pastan,et al. Modulation of activity of the promoter of the human MDR1 gene by Ras and p53. , 1992, Science.
[153] M. Subler,et al. Modulation of cellular and viral promoters by mutant human p53 proteins found in tumor cells , 1992, Journal of virology.
[154] A. Chicas,et al. Mutant p53 forms a complex with Sp1 on HIV-LTR DNA. , 2000, Biochemical and biophysical research communications.
[155] W. Deppert,et al. Mutant p53 proteins bind DNA in a DNA structure-selective mode , 2005, Nucleic acids research.
[156] C. Prives,et al. The p53 pathway , 1999, The Journal of pathology.
[157] A. Børresen-Dale,et al. TP53 mutations in human cancers: functional selection and impact on cancer prognosis and outcomes , 2007, Oncogene.
[158] D. Ledbetter,et al. Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas. , 1989, Science.
[159] V. Rotter. p53, a transformation-related cellular-encoded protein, can be used as a biochemical marker for the detection of primary mouse tumor cells. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[160] E. White,et al. Does control of mutant p53 by Mdm2 complicate cancer therapy? , 2008, Genes & development.
[161] A. Chicas,et al. p53 represses Sp1 DNA binding and HIV-LTR directed transcription. , 1997, Cellular and molecular biology.
[162] J. Bergh,et al. The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer. , 2006, Clinical cancer research : an official journal of the American Association for Cancer Research.
[163] G. Evan,et al. Temporal dissection of p53 function in vitro and in vivo , 2005, Nature Genetics.
[164] T. Jacks,et al. The role of p53 in tumour suppression: lessons from mouse models , 1999, Cellular and Molecular Life Sciences CMLS.
[165] M. Scian,et al. Tumor-Derived p53 Mutants Induce NF-κB2 Gene Expression , 2005, Molecular and Cellular Biology.
[166] S. Kato,et al. Understanding the function–structure and function–mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[167] G. Evan,et al. The pathological response to DNA damage does not contribute to p53-mediated tumour suppression , 2006, Nature.
[168] V. Rotter,et al. ChIP-on-chip analysis of in vivo mutant p53 binding to selected gene promoters. , 2011, Omics : a journal of integrative biology.
[169] J. Cleveland,et al. Activation of c-myc Gene Expression by Tumor-Derived p53 Mutants Requires a Discrete C-Terminal Domain , 1998, Molecular and Cellular Biology.
[170] E. Kim,et al. Interactions of mutant p53 with DNA: guilt by association , 2007, Oncogene.
[171] Galina Selivanova,et al. Characterization of the p53-rescue drug CP-31398 in vitro and in living cells , 2002, Oncogene.
[172] S. Lindquist,et al. Heat Shock Factor 1 Is a Powerful Multifaceted Modifier of Carcinogenesis , 2007, Cell.
[173] Wensheng Yan,et al. Characterization of Functional Domains Necessary for Mutant p53 Gain of Function*♦ , 2010, The Journal of Biological Chemistry.
[174] V. Rotter,et al. Transcription regulation by mutant p53 , 2007, Oncogene.
[175] A. Levine,et al. Characterization of a 54K Dalton cellular SV40 tumor antigen present in SV40-transformed cells and uninfected embryonal carcinoma cells , 1979, Cell.
[176] Gang Li,et al. Cancer chemoresistance: The relationship between p53 and multidrug transporters , 2002, International journal of cancer.
[177] D. Ginsberg,et al. p53 and E2f: partners in life and death , 2009, Nature Reviews Cancer.
[178] J. Bartek,et al. Genetic and immunochemical analysis of mutant p53 in human breast cancer cell lines. , 1990, Oncogene.
[179] C. Bonaïti‐pellié,et al. Molecular basis of the Li–Fraumeni syndrome: an update from the French LFS families , 2008, Journal of Medical Genetics.
[180] M Bycroft,et al. Hot-spot mutants of p53 core domain evince characteristic local structural changes. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[181] A. Bernstein,et al. Inactivation of the p53 oncogene by internal deletion or retroviral integration in erythroleukemic cell lines induced by Friend leukemia virus. , 1988, Oncogene.
[182] Frank M Boeckler,et al. Targeted rescue of a destabilized mutant of p53 by an in silico screened drug , 2008, Proceedings of the National Academy of Sciences.
[183] S. Soddu,et al. Gal‐3 is stimulated by gain‐of‐function p53 mutations and modulates chemoresistance in anaplastic thyroid carcinomas , 2009, The Journal of pathology.
[184] P. Jeffrey,et al. Crystal structure of a p53 tumor suppressor-DNA complex: understanding tumorigenic mutations. , 1994, Science.
[185] Eduardo Sontag,et al. Transcriptional control of human p53-regulated genes , 2008, Nature Reviews Molecular Cell Biology.
[186] Anindita Das,et al. Tumor-derived p53 mutants induce oncogenesis by transactivating growth-promoting genes , 2004, Oncogene.
[187] Xin Lu,et al. Live or let die: the cell's response to p53 , 2002, Nature Reviews Cancer.
[188] A. Levine,et al. Two critical hydrophobic amino acids in the N-terminal domain of the p53 protein are required for the gain of function phenotypes of human p53 mutants. , 1995, Oncogene.
[189] A. Levine,et al. Gain of function mutations in p53 , 1993, Nature Genetics.
[190] C. Prives,et al. Human tumor-derived p53 proteins exhibit binding site selectivity and temperature sensitivity for transactivation in a yeast-based assay , 1998, Oncogene.
[191] A. Multani,et al. Chromosome stability, in the absence of apoptosis, is critical for suppression of tumorigenesis in Trp53 mutant mice , 2004, Nature Genetics.
[192] B. Vogelstein,et al. p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis. , 1990, Cancer research.
[193] L. Vassilev,et al. Small-molecule inhibitors of the p53-MDM2 interaction. , 2011, Current topics in microbiology and immunology.
[194] M. Oren,et al. Wild-type p53 can inhibit oncogene-mediated focus formation. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[195] A. Levine,et al. Mutation is required to activate the p53 gene for cooperation with the ras oncogene and transformation , 1989, Journal of virology.
[196] G. Wahl,et al. A mouse p53 mutant lacking the proline-rich domain rescues Mdm4 deficiency and provides insight into the Mdm2-Mdm4-p53 regulatory network. , 2006, Cancer cell.
[197] Michael A. Dyer,et al. MDMX: from bench to bedside , 2007, Journal of Cell Science.
[198] C. Coffill,et al. The role of mutant p53 in human cancer , 2011, The Journal of pathology.
[199] A. Levine,et al. Novel gain of function activity of p53 mutants: activation of the dUTPase gene expression leading to resistance to 5-fluorouracil , 2002, Oncogene.
[200] D. Bell,et al. Noncanonical DNA Motifs as Transactivation Targets by Wild Type and Mutant p53 , 2008, PLoS genetics.
[201] D. Lane,et al. Reactivation of p53: from peptides to small molecules. , 2011, Trends in pharmacological sciences.
[202] B. Foster,et al. Pharmacological rescue of mutant p53 conformation and function. , 1999, Science.
[203] A. Levine,et al. Surfing the p53 network , 2000, Nature.