p16(MTS-1/CDKN2/INK4a) in cancer progression.

Since its discovery as an inhibitor of cyclin-dependent kinases 4 and 6, the tumor suppressor p16 has continued to gain widespread importance in cancer. The high frequency of deletions of p16 in tumor cell lines first suggested an important role for p16 in carcinogenesis. This initial genetic evidence was subsequently strengthened by numerous studies documenting p16 inactivation in kindreds with familial melanoma. Moreover, a high frequency of p16 gene alterations was found in primary tumors, while recent studies have identified p16 promoter methylation as a major mechanism of tumor-suppressor-gene silencing. Additional insight into p16's role in cancer has come from the genetic analysis of precancerous lesions and various tissue culture models. It is now believed that loss of p16 is an early and often critical event in tumor progression. Consequently, p16 is a major tumor-suppressor gene whose frequent loss occurs early in many human cancers.

[1]  Santoro,et al.  p16 (INK4a, MTS‐1) gene polymorphism and methylation status in human pituitary tumours , 1999, Clinical endocrinology.

[2]  M. Serrano,et al.  A p16INK4a-insensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma , 1995, Science.

[3]  J. Herman,et al.  Gene promoter hypermethylation in tumors and serum of head and neck cancer patients. , 2000, Cancer research.

[4]  K. Post,et al.  Frequent loss of the P16INK4a gene product in human pituitary tumors. , 1996, Cancer research.

[5]  M. Haas,et al.  Independent induction of senescence by p16INK4a and p21CIP1 in spontaneously immortalized human fibroblasts. , 1998, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[6]  M. Williamson,et al.  p16 (CDKN2) is a major deletion target at 9p21 in bladder cancer. , 1995, Human molecular genetics.

[7]  G. Basso,et al.  Analysis of cyclin‐dependent kinase inhibitor genes (CDKN2A, CDKN2B, and CDKN2C) in childhood rhabdomyosarcoma , 1996, Genes, chromosomes & cancer.

[8]  J. A. Bishop,et al.  Genetic heterogeneity in familial malignant melanoma. , 1994, Human molecular genetics.

[9]  C. Weghorst,et al.  Frequent Mutation of p16 in Squamous Cell Carcinoma of the Head and Neck , 1998, The Laryngoscope.

[10]  J. Moul,et al.  Mutations of the p16 gene product are rare in prostate cancer , 1997, The Prostate.

[11]  T. Kumanishi,et al.  Primary Malignant Lymphoma of the Brain: Demonstration of Frequent p16 and p15 Gene Deletions , 1996, Japanese journal of cancer research : Gann.

[12]  M. Newton,et al.  Overcoming cellular senescence in human cancer pathogenesis. , 1998, Genes & development.

[13]  M. Beckmann,et al.  CDKN2A gene inactivation in epithelial sporadic ovarian cancer , 1999, British Journal of Cancer.

[14]  O. Olopade,et al.  Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia. , 1994, Cancer research.

[15]  C. Sherr The Pezcoller lecture: cancer cell cycles revisited. , 2000, Cancer research.

[16]  J. Jen,et al.  Cyclin D1 amplification is independent of p16 inactivation in head and neck squamous cell carcinoma , 1999, Oncogene.

[17]  Å. Borg,et al.  High Frequency of Multiple Melanomas and Breast and Pancreas Carcinomas in CDKN2A Mutation-Positive Melanoma Families , 2000 .

[18]  Ashutosh Kumar Singh,et al.  Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene, CDK4I, in melanoma. , 1994, Cancer research.

[19]  R. Dahse,et al.  Tumor suppressor gene p16 (CDKN2A) mutation status and promoter inactivation in head and neck cancer. , 1999, International journal of molecular medicine.

[20]  Y. Hayashi,et al.  Homozygous deletions of p16/MTS1 and p15/MTS2 genes are frequent in t(1;19)-negative but not in t(1;19)-positive B precursor acute lymphoblastic leukemia in childhood. , 1996, Leukemia.

[21]  F. Sigaux,et al.  Candidate tumor-suppressor genes MTS1 (p16INK4A) and MTS2 (p15INK4B) display frequent homozygous deletions in primary cells from T- but not from B-cell lineage acute lymphoblastic leukemias. , 1994, Blood.

[22]  M. Newton,et al.  p16/pRb pathway alterations are required for bypassing senescence in human prostate epithelial cells. , 1999, Cancer research.

[23]  D. Sidransky,et al.  p16INK4A adenovirus-mediated gene therapy for human head and neck squamous cell cancer. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.

[24]  T. Shuin,et al.  Infrequent somatic mutations of the p16 and p15 genes in human bladder cancer: p16 mutations occur only in low-grade and superficial bladder cancers. , 1995, Oncology research.

[25]  H. Watanabe,et al.  Genetic progression and divergence in pancreatic carcinoma. , 2000, The American journal of pathology.

[26]  T. Manshouri,et al.  p16INK4A and p15INK4B gene deletions in primary leukemias. , 1995, Blood.

[27]  R. Maestro,et al.  p16/CDKN2 and CDK4 gene mutations in sporadic melanoma development and progression , 1997, International journal of cancer.

[28]  The genetics of hereditary melanoma and nevi , 1999, Cancer.

[29]  K. Ichimura,et al.  Deregulation of the p14ARF/MDM2/p53 pathway is a prerequisite for human astrocytic gliomas with G1-S transition control gene abnormalities. , 2000, Cancer research.

[30]  Gordon B Mills,et al.  Expression of p16 induces transcriptional downregulation of the RB gene , 1998, Oncogene.

[31]  A. Hagemeijer,et al.  Analysis of the P53, RB/D13S25, and P16 tumor suppressor genes in marginal zone B-cell lymphoma: An interphase fluorescence in situ hybridization study. , 2000, Cancer genetics and cytogenetics.

[32]  G. Yang,et al.  Mechanisms of inactivation of p14ARF, p15INK4b, and p16INK4a genes in human esophageal squamous cell carcinoma. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.

[33]  W. Cavenee,et al.  Functional analysis of wild-type and malignant glioma derived CDKN2Aβ alleles: Evidence for an RB-independent growth suppressive pathway , 1997, Oncogene.

[34]  C. D. Edwards,et al.  Multiple mechanisms of p16INK4A inactivation in non-small cell lung cancer cell lines. , 1995, Cancer research.

[35]  H. Koeffler,et al.  Alterations of the p15, p16,and p18 genes in osteosarcoma. , 1996, Cancer genetics and cytogenetics.

[36]  H. Matsuda,et al.  Inversely correlated expression of p16 and Rb protein in non‐small cell lung cancers: An immunohistochemical study , 1996, International journal of cancer.

[37]  M. Roussel,et al.  Cooperative Signals Governing ARF-Mdm2 Interaction and Nucleolar Localization of the Complex , 2000, Molecular and Cellular Biology.

[38]  J. Decaprio,et al.  Loss of p19ARF Eliminates the Requirement for the pRB-Binding Motif in Simian Virus 40 Large T Antigen-Mediated Transformation , 2000, Molecular and Cellular Biology.

[39]  D. Miller,et al.  Incidence of p14ARF gene deletion in high-grade adult and pediatric astrocytomas. , 2000, Human pathology.

[40]  Peter A. Jones,et al.  Early acquisition of homozygous deletions of p16/p19 during squamous cell carcinogenesis and genetic mosaicism in bladder cancer , 1998, Oncogene.

[41]  G. Enders,et al.  p16INK4a can initiate an autonomous senescence program , 2000, Oncogene.

[42]  J. Cairns,et al.  A comparison between microsatellite and quantitative PCR analyses to detect frequent p16 copy number changes in primary bladder tumors. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.

[43]  J. Benítez,et al.  Loss of p16/INK4A protein expression in non-Hodgkin's lymphomas is a frequent finding associated with tumor progression. , 1998, The American journal of pathology.

[44]  J. Bartek,et al.  High frequency of p16 (CDKN2/MTS-1/INK4A) inactivation in head and neck squamous cell carcinoma. , 1996, Cancer research.

[45]  M. Link,et al.  Frequent and selective methylation of p15 and deletion of both p15 and p16 in T-cell acute lymphoblastic leukemia. , 1997, Cancer research.

[46]  R. deVere White,et al.  Frequent alteration of CDKN2 (p16(INK4A)/MTS1) expression in human primary prostate carcinomas. , 1997, Clinical cancer research : an official journal of the American Association for Cancer Research.

[47]  K. Kinzler,et al.  Deletion of p16 and p15 genes in brain tumors. , 1994, Cancer research.

[48]  I. Jacobs,et al.  No evidence exists for methylation inactivation of the p16 tumor suppressor gene in ovarian carcinogenesis. , 1998, Gynecologic oncology.

[49]  J. D. Weber,et al.  The ARF/p53 pathway. , 2000, Current opinion in genetics & development.

[50]  Richard A. Ashmun,et al.  Tumor Suppression at the Mouse INK4a Locus Mediated by the Alternative Reading Frame Product p19 ARF , 1997, Cell.

[51]  K. Goi,et al.  p16/MTS1/INK4A gene is frequently inactivated by hypermethylation in childhood acute lymphoblastic leukemia with 11q23 translocation , 1999, Leukemia.

[52]  W. Hahn,et al.  Human Keratinocytes That Express hTERT and Also Bypass a p16INK4a-Enforced Mechanism That Limits Life Span Become Immortal yet Retain Normal Growth and Differentiation Characteristics , 2000, Molecular and Cellular Biology.

[53]  J. Herman,et al.  Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[54]  O. Olopade,et al.  Detection of CDKN2 deletions in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization. , 1995, Cancer research.

[55]  D. Grandér,et al.  Involvement of the Ink4 proteins p16 and p15 in T-lymphocyte senescence , 1998, Oncogene.

[56]  N. Dyson,et al.  Requirements for cell cycle arrest by p16INK4a. , 2000, Molecular cell.

[57]  W. Clark,et al.  Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity. , 1994, American journal of human genetics.

[58]  O. Olopade,et al.  Codeletion of CDKN2 and MTAP genes in a subset of non‐Hodgkin's lymphoma may be associated with histologic transformation from low‐grade to diffuse large‐cell lymphoma , 1998, Genes, chromosomes & cancer.

[59]  A M Goldstein,et al.  Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations. , 1995, The New England journal of medicine.

[60]  R. DePinho,et al.  The INK4A/ARF locus and its two gene products. , 1999, Current opinion in genetics & development.

[61]  L. Chin,et al.  Role of the INK4a Locus in Tumor Suppression and Cell Mortality , 1996, Cell.

[62]  C. Weghorst,et al.  p16 mutation frequency and clinical correlation in head and neck cancer. , 1999, Acta oto-laryngologica.

[63]  Y. Bignon,et al.  p16 involvement in primary bladder tumors: analysis of deletions and mutations. , 1999, International journal of oncology.

[64]  D. Wong,et al.  p16INK4a promoter is hypermethylated at a high frequency in esophageal adenocarcinomas. , 1997, Cancer research.

[65]  M. Toyota,et al.  Distinct methylation pattern and microsatellite instability in sporadic gastric cancer , 1999, International journal of cancer.

[66]  M. Nagai,et al.  High prevalence of p16 genetic alterations in head and neck tumours , 1999, British Journal of Cancer.

[67]  C. Bréchot,et al.  Alterations of cyclin-dependent kinase 4 inhibitor (p16INK4A/MTS1) gene structure and expression in acute lymphoblastic leukemias. , 1995, Leukemia.

[68]  N. Gruis,et al.  Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16‐Leiden) , 2000, International journal of cancer.

[69]  A. El‐Naggar,et al.  Methylation, a major mechanism of p16/CDKN2 gene inactivation in head and neck squamous carcinoma. , 1997, The American journal of pathology.

[70]  H. Koeffler,et al.  Deletions of the cyclin-dependent kinase inhibitor genes p16INK4A and p15INK4B in non-Hodgkin's lymphomas. , 1995, Blood.

[71]  D. Carson,et al.  Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers , 1994, Nature.

[72]  J. Minna,et al.  Correlation of abnormal RB, p16ink4a, and p53 expression with 3p loss of heterozygosity, other genetic abnormalities, and clinical features in 103 primary non-small cell lung cancers. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.

[73]  G. Peters,et al.  The p16INK4a/CDKN2A tumor suppressor and its relatives. , 1998, Biochimica et biophysica acta.

[74]  B. Peters,et al.  Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds. , 1995, Oncogene.

[75]  C. Reznikoff,et al.  Elevated p16 at senescence and loss of p16 at immortalization in human papillomavirus 16 E6, but not E7, transformed human uroepithelial cells. , 1996, Cancer research.

[76]  J. Herman,et al.  Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers. , 1995, Cancer research.

[77]  O. Olopade,et al.  Preferential loss of expression of p16(INK4a) rather than p19(ARF) in breast cancer. , 1996, Clinical cancer research : an official journal of the American Association for Cancer Research.

[78]  A. Brenner,et al.  Chromosome 9p allelic loss and p16/CDKN2 in breast cancer and evidence of p16 inactivation in immortal breast epithelial cells. , 1995, Cancer research.

[79]  A. Okamoto,et al.  Mutations and altered expression of p16INK4 in human cancer. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[80]  M. Hollstein,et al.  Low frequency of p16/CDKN2 gene mutations in esophageal carcinomas , 1996, International journal of cancer.

[81]  J. Schalken,et al.  p16 mutations/deletions are not frequent events in prostate cancer. , 1996, British Journal of Cancer.

[82]  Manuel Serrano,et al.  Crystal structure of the complex of the cyclin D-dependent kinase Cdk6 bound to the cell-cycle inhibitor p19INK4d , 1998, Nature.

[83]  R. Reddel,et al.  p16(INK4a) and the control of cellular proliferative life span. , 1999, Carcinogenesis.

[84]  G. Chenevix-Trench,et al.  Rare mutations and no hypermethylation at the CDKN2A locus in epithelial ovarian tumours , 1997, International journal of cancer.

[85]  D. Sidransky,et al.  Rates of p16 (MTS1) mutations in primary tumors with 9p loss. , 1994, Science.

[86]  W. Baek,et al.  Lack of mutation at p16INK4A gene but expression of aberrant p16INK4A RNA transcripts in human ovarian carcinoma. , 2000, Cancer letters.

[87]  Zhiming He,et al.  LMP1 of Epstein–Barr virus suppresses cellular senescence associated with the inhibition of p16INK4a expression , 2000, Oncogene.

[88]  G. Hannon,et al.  Deletion of the p16 and p15 genes in human bladder tumors. , 1995, Journal of the National Cancer Institute.

[89]  J. Herman,et al.  Inactivation of the INK4A/ARF locus frequently coexists with TP53 mutations in non-small cell lung cancer , 1999, Oncogene.

[90]  S. Groshen,et al.  High frequency of simultaneous loss of p16 and p16β gene expression in squamous cell carcinoma of the esophagus but not in adenocarcinoma of the esophagus or stomach , 1997, Oncogene.

[91]  François G. Meyer,et al.  Deletions of the INK4A gene in superficial bladder tumors. Association with recurrence. , 1999, The American journal of pathology.

[92]  M. Ogawa,et al.  Somatic mutations of the MTS (multiple tumor suppressor) 1/CDK4l (cyclin-dependent kinase-4 inhibitor) gene in human primary non-small cell lung carcinomas. , 1994, Biochemical and biophysical research communications.

[93]  M. González,et al.  Deletions and rearrangements of cyclin-dependent kinase 4 inhibitor gene p16 are associated with poor prognosis in B cell non-Hodgkin’s lymphomas , 1997, Leukemia.

[94]  R. Weinberg,et al.  Growth suppression by p16ink4 requires functional retinoblastoma protein. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[95]  W. Farrell,et al.  Hypermethylation of the p16/CDKN2A/MTS1 gene and loss of protein expression is associated with nonfunctional pituitary adenomas but not somatotrophinomas , 1999, Genes, chromosomes & cancer.

[96]  M. Noguchi,et al.  DNA methylation and expression of p16INK4A gene in pulmonary adenocarcinoma and anthracosis in background lung , 1999, International journal of cancer.

[97]  D. Sidransky,et al.  Analysis of p16 (CDKN2/MTS-1/INK4A) alterations in primary sporadic uveal melanoma. , 1999, Investigative ophthalmology & visual science.

[98]  B. Wiedenmann,et al.  A Novel Function for the Tumor Suppressor p16INK4a , 2000, The Journal of Cell Biology.

[99]  B. Quesnel,et al.  Analysis of p16 gene deletion and point mutation in breast carcinoma. , 1995, British Journal of Cancer.

[100]  T. Taki,et al.  Hypermethylation of p16 and p15 genes and RB protein expression in acute leukemia. , 2000, Leukemia research.

[101]  G. Hannon,et al.  A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4 , 1993, Nature.

[102]  J. Slater,et al.  Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis , 1997, Leukemia.

[103]  S. Baylin,et al.  Aberrant methylation in gastric cancer associated with the CpG island methylator phenotype. , 1999, Cancer research.

[104]  D. Beach,et al.  p16INK4A and p19ARF act in overlapping pathways in cellular immortalization , 2000, Nature Cell Biology.

[105]  M. Steiner,et al.  Adenoviral vector containing wild-type p16 suppresses prostate cancer growth and prolongs survival by inducing cell senescence , 2000, Cancer Gene Therapy.

[106]  K. Hoang-Xuan,et al.  Frequent loss of heterozygosity on chromosome 9, and low incidence of mutations of cyclin-dependent kinase inhibitors p15 (MTS2) and p16 (MTS1) genes in gliomas. , 1995, Oncogene.

[107]  Y. Matsumura,et al.  Mutations of p16 and p15 tumor suppressor genes and replication errors contribute independently to the pathogenesis of sporadic malignant melanoma , 1998, Archives of Dermatological Research.

[108]  S. Ogawa,et al.  Loss of the cyclin-dependent kinase 4-inhibitor (p16; MTS1) gene is frequent in and highly specific to lymphoid tumors in primary human hematopoietic malignancies. , 1995, Blood.

[109]  D. Louis,et al.  Frequent disruption of the RB1 pathway in diffuse large B cell lymphoma: prognostic significance of E2F-1 and p16INK4A , 2000, Leukemia.

[110]  G. Peters,et al.  Regulation of p16CDKN2 expression and its implications for cell immortalization and senescence , 1996, Molecular and cellular biology.

[111]  P. Heinzel,et al.  Mutations and polymorphisms in the p53, p21 and p16 genes in oral carcinomas of Indian betel quid chewers , 1996, International journal of cancer.

[112]  K. Magnússon,et al.  p16/INK4a and p15/INK4b gene methylation and absence of p16/INK4a mRNA and protein expression in Burkitt's lymphoma. , 1998, Blood.

[113]  Ken Chen,et al.  The Ink4a Tumor Suppressor Gene Product, p19Arf, Interacts with MDM2 and Neutralizes MDM2's Inhibition of p53 , 1998, Cell.

[114]  T. Dryja,et al.  Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene. , 1991, American journal of human genetics.

[115]  Philip D. Jeffrey,et al.  Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a , 1998, Nature.

[116]  J. Jen,et al.  Detailed deletion mapping at chromosome 9p21 in non‐small cell lung cancer by microsatellite analysis and fluorescence in situ hybridization , 1997, International journal of cancer.

[117]  Y. Hayashi,et al.  Homozygous deletions of p16/MTS1 gene are frequent but mutations are infrequent in childhood T-cell acute lymphoblastic leukemia. , 1995, Blood.

[118]  J. Felix,et al.  Differences inp16Gene Methylation and Expression in Benign and Malignant Ovarian Tumors , 1999 .

[119]  L. Hayflick,et al.  The serial cultivation of human diploid cell strains. , 1961, Experimental cell research.

[120]  A. Mes-Masson,et al.  Analysis of the p16 tumor suppressor gene in early‐stage prostate cancer , 1998, Molecular carcinogenesis.

[121]  R. Schneider-Stock,et al.  Gene alterations at the CDKN2A (p16/MTS1) locus in soft tissue tumors. , 1998, International journal of oncology.

[122]  Peter A. Jones,et al.  P16 gene in uncultured tumours , 1994, Nature.

[123]  L. Sandkuijl,et al.  Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds , 1995, Nature Genetics.

[124]  P. Malfertheiner,et al.  Alterations of the p16/MTS1-tumor suppressor gene in gastric cancer. , 1998, Pathology, research and practice.

[125]  B. Vogelstein,et al.  A genetic model for colorectal tumorigenesis , 1990, Cell.

[126]  H. Höfler,et al.  CDKN2a/p16INK4a mutations and lack of p19ARF involvement in familial melanoma kindreds. , 1998, The Journal of investigative dermatology.

[127]  P. Carroll,et al.  Frequent homozygous deletion of cyclin‐dependent kinase inhibitor 2 (MTS1, p16) in superficial bladder cancer detected by fluorescence in situ hybridization , 1997, Genes, chromosomes & cancer.

[128]  A. Scarpa,et al.  Molecular features of primary mediastinal B‐cell lymphoma: involvement of p16INK4A, p53 and c‐myc , 1999, British journal of haematology.

[129]  D. Louis,et al.  CDKN2A gene deletions and loss of p16 expression occur in osteosarcomas that lack RB alterations. , 1998, The American journal of pathology.

[130]  H. Drexler Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia–lymphoma cells , 1998, Leukemia.

[131]  M. Skolnick,et al.  A cell cycle regulator potentially involved in genesis of many tumor types. , 1994, Science.

[132]  E. Healy,et al.  Infrequent mutation of p16INK4 in sporadic melanoma. , 1996, The Journal of investigative dermatology.

[133]  D. Louis,et al.  CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated. , 1996, Cancer research.

[134]  O. Olopade,et al.  p16 alterations and deletion mapping of 9p21-p22 in malignant mesothelioma. , 1994, Cancer research.

[135]  A. Okamoto,et al.  IS-12 Mutation and altered expression of P16^ in human cancer. , 1995 .

[136]  T. Nakajima,et al.  An immunohistochemical study of p16, pRb, p21 and p53 proteins in human esophageal cancers. , 2000, Anticancer research.

[137]  J. Barrett,et al.  Homozygous deletions at chromosome 9p21 and mutation analysis of p16 and p15 in microdissected primary non-small cell lung cancers. , 1995, Clinical cancer research : an official journal of the American Association for Cancer Research.

[138]  M. Skolnick,et al.  Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus , 1994, Nature Genetics.

[139]  X. Estivill,et al.  Retention of the CDKN2A locus and low frequency of point mutations in primary and metastasic cutaneous malignant melanoma , 1998, International journal of cancer.

[140]  Adrian Bird,et al.  The essentials of DNA methylation , 1992, Cell.

[141]  A. Brenner,et al.  Increased p16 expression with first senescence arrest in human mammary epithelial cells and extended growth capacity with p16 inactivation , 1998, Oncogene.

[142]  J. Foekens,et al.  Sporadic CDKN2 (MTS1/p16ink4) gene alterations in human ovarian tumours. , 1996, British Journal of Cancer.

[143]  Y. Bang,et al.  Alterations of p16INK4A and p15INK4B genes in gastric carcinomas , 1997, Cancer.

[144]  M. Diccianni,et al.  p16INK4 and p15INK4B alterations in primary gynecologic malignancy. , 1997, Gynecologic oncology.

[145]  M. Yuille,et al.  Deletions and rearrangement of CDKN2 in lymphoid malignancy. , 1995, Blood.

[146]  J. Abraham,et al.  The MTS1 gene is frequently mutated in primary human esophageal tumors. , 1994, Oncogene.

[147]  J. R. Smith,et al.  Complex mechanisms underlying impaired activation of Cdk4 and Cdk2 in replicative senescence: roles of p16, p21, and cyclin D1. , 1999, Experimental cell research.

[148]  E. Campo,et al.  p16(INK4a) gene inactivation by deletions, mutations, and hypermethylation is associated with transformed and aggressive variants of non-Hodgkin's lymphomas. , 1998, Blood.

[149]  M. Tomonaga,et al.  Homozygous deletions of the p15 (MTS2) and p16 (CDKN2/MTS1) genes in adult T-cell leukemia. , 1995, Blood.

[150]  J. Bartek,et al.  Retinoblastoma-protein-dependent cell-cycle inhibition by the tumour suppressor p16 , 1995, Nature.

[151]  D. Louis,et al.  Molecular Genetic Correlates of p16, cdk4, and pRb Immunohistochemistry in Glioblastomas , 1998, Journal of neuropathology and experimental neurology.

[152]  T. Enomoto,et al.  Alteration of p16 and p15 genes in common epithelial ovarian tumors , 1997, International journal of cancer.

[153]  S. Nishizuka,et al.  Inactivation of the CDKN2 gene by homozygous deletion and de novo methylation is associated with advanced stage esophageal squamous cell carcinoma. , 1996, Cancer research.

[154]  R. Rimokh,et al.  Molecular analysis of cyclin-dependent kinase inhibitors in human leukemias , 1997, Leukemia.

[155]  J. Bruner,et al.  Mutations of the p16 gene in gliomas. , 1996, Oncogene.

[156]  F. Mandelli,et al.  Detection of homozygous deletions of the cyclin-dependent kinase 4 inhibitor (p16) gene in acute lymphoblastic leukemia and association with adverse prognostic features. , 1995, Blood.

[157]  J. Herman,et al.  Deletional, mutational, and methylation analyses of CDKN2 (p16/MTS1) in primary and metastatic prostate cancer , 1997, Genes, chromosomes & cancer.

[158]  C. Moskaluk,et al.  Abrogation of the Rb/p16 tumor-suppressive pathway in virtually all pancreatic carcinomas. , 1997, Cancer research.

[159]  K. Hirokawa,et al.  Induction of the p16INK4a senescence gene as a new therapeutic strategy for the treatment of rheumatoid arthritis , 1999, Nature Medicine.

[160]  B. Quesnel,et al.  p16 gene homozygous deletions in acute lymphoblastic leukemia. , 1995, Blood.

[161]  I. Wong,et al.  Aberrant p15 promoter methylation in adult and childhood acute leukemias of nearly all morphologic subtypes: potential prognostic implications. , 2000, Blood.

[162]  G. Kang,et al.  Correlation of p16 Hypermethylation with p16 Protein Loss in Sporadic Gastric Carcinomas , 2000, Laboratory Investigation.

[163]  P. Picci,et al.  Alteration of pRb/p16/cdk4 regulation in human osteosarcoma , 1999, International journal of cancer.

[164]  E. Newcomb,et al.  Alterations of multiple tumor suppressor genes (p53 (17p13), p16INK4 (9p21), and DBM (13q14)) in B‐CELL chronic lymphocytic leukemia , 1995, Molecular carcinogenesis.

[165]  S. Mori,et al.  Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma. , 1994, Cancer research.

[166]  M. Miwa,et al.  Inactivation of p16/CDKN2 and p15/MTS2 genes in different histological types and clinical stages of primary ovarian tumors , 1996, International journal of cancer.

[167]  Goos,et al.  Homozygous deletion of the p16INK4a and the p15INK4b tumour suppressor genes in a subset of human sporadic cutaneous malignant melanoma , 1998, The British journal of dermatology.

[168]  M. Berger,et al.  Silencing of p16/CDKN2 expression in human gliomas by methylation and chromatin condensation. , 1996, Cancer research.

[169]  F. Bosman,et al.  Frequent methylation silencing of p15(INK4b) (MTS2) and p16(INK4a) (MTS1) in B-cell and T-cell lymphomas. , 1999, Blood.

[170]  G. Finocchiaro,et al.  Mutation rate of the CDKN2 gene in malignant gliomas. , 1994, Cancer research.

[171]  J. Rüschoff,et al.  Molecular analysis of microdissected tumors and preneoplastic intraductal lesions in pancreatic carcinoma. , 2000, The American journal of pathology.

[172]  G. Peters,et al.  Role of the alternative INK4A proteins in human keratinocyte senescence: evidence for the specific inactivation of p16INK4A upon immortalization. , 1999, Cancer research.

[173]  J. Fletcher,et al.  Codeletion of p15 and p16 in primary malignant mesothelioma. , 1995, Oncogene.

[174]  D. Sidransky Cancer genetics: Two tracks but one race? , 1996, Current Biology.

[175]  H. Koeffler,et al.  Molecular analysis of the INK4 family of genes in prostate carcinomas. , 1997, The Journal of urology.

[176]  J. Herman,et al.  5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers , 1995, Nature Medicine.

[177]  F. Sigaux,et al.  Genomic alterations of the p19ARF encoding exons in T-cell acute lymphoblastic leukemia. , 1998, Blood.

[178]  P. V. van Helden,et al.  p53 and p16/CDKN2 gene mutations in esophageal tumors from a high‐incidence area in South Africa , 1998, International journal of cancer.

[179]  R. Hruban,et al.  Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma , 1994, Nature Genetics.

[180]  G. Yang,et al.  Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China. , 1999, Carcinogenesis.

[181]  R. Blamey,et al.  INK4a gene expression and methylation in primary breast cancer: overexpression of p16INK4a messenger RNA is a marker of poor prognosis. , 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

[182]  A. Takaoka,et al.  Infrequent alterations of the p16 (MTS-1) gene in human gastric cancer. , 1997, Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine.

[183]  B. Migeon Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa. , 1990, Genetical research.

[184]  D. Gonzalez,et al.  De novo methylation of tumor suppressor gene p16/INK4a is a frequent finding in multiple myeloma patients at diagnosis , 2000, Leukemia.

[185]  S. Sakaki,et al.  Restoration of wild-type p16 down-regulates vascular endothelial growth factor expression and inhibits angiogenesis in human gliomas. , 1999, Cancer research.

[186]  G. Wei,et al.  Prognostic impact of INK4A deletion in Ewing sarcoma , 2000, Cancer.

[187]  M. Takata,et al.  p16INK4a inactivation is not frequent in uncultured sporadic primary cutaneous melanoma , 1999, Oncogene.

[188]  B. Min,et al.  Concurrence of replicative senescence and elevated expression of p16(INK4A) with subculture-induced but not calcium-induced differentiation in normal human oral keratinocytes. , 2000, Archives of oral biology.

[189]  F. Sigaux,et al.  Multiple tumor-suppressor gene 1 inactivation is the most frequent genetic alteration in T-cell acute lymphoblastic leukemia. , 1996, Blood.

[190]  T. Löning,et al.  p16/MTS1 inactivation in ovarian carcinomas: High frequency of reduced protein expression associated with hyper‐methylation or mutation in endometrioid and mucinous tumors , 1998, International journal of cancer.

[191]  K. Buetow,et al.  Characterization of chromosome 9 in human ovarian neoplasia identifies frequent genetic imbalance on 9q and rare alterations involving 9p, including CDKN2. , 1995, Cancer research.

[192]  G. Hannon,et al.  Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[193]  T. Kumanishi,et al.  Frequent deletion and 5' CpG island methylation of the p16 gene in primary malignant lymphoma of the brain. , 1998, Cancer research.

[194]  M. Piris,et al.  Loss of p16 protein expression associated with methylation of the p16INK4A gene is a frequent finding in Hodgkin's disease. , 1999, Laboratory investigation; a journal of technical methods and pathology.

[195]  G. Wei,et al.  CDK4 gene amplification in osteosarcoma: Reciprocal relationship with INK4A gene alterations and mapping of 12q13 amplicons , 1999, International journal of cancer.

[196]  G. Hannon,et al.  Mutations in the p16INK4/MTS1/CDKN2, p15INK4B/MTS2, and p18 genes in primary and metastatic lung cancer. , 1995, Cancer research.

[197]  S. Ogawa,et al.  Inactivation of multiple tumor-suppressor genes involved in negative regulation of the cell cycle, MTS1/p16INK4A/CDKN2, MTS2/p15INK4B, p53, and Rb genes in primary lymphoid malignancies. , 1996, Blood.

[198]  K. Tanaka,et al.  Homozygous loss of the cyclin-dependent kinase 4-inhibitor (p16) gene in human leukemias. , 1994, Blood.

[199]  A. Scharl,et al.  Expression of p16 and lack of pRB in primary small cell lung cancer , 1999, The Journal of pathology.

[200]  W. Clark,et al.  Germline p16 mutations in familial melanoma , 1994, Nature Genetics.

[201]  Kathleen R. Cho,et al.  Frequency of homozygous deletion at p16/CDKN2 in primary human tumours , 1995, Nature Genetics.

[202]  A. Patiño-García,et al.  Analysis of the p16INK4 and TP53 tumor suppressor genes in bone sarcoma pediatric patients. , 1997, Cancer genetics and cytogenetics.

[203]  J. Califano,et al.  11:40 AM: A Genetic Progression Model for Head and Neck Cancer: Implications for Field Cancerization , 1996 .

[204]  F. Zindy,et al.  Inhibition of cyclin D1 phosphorylation on threonine-286 prevents its rapid degradation via the ubiquitin-proteasome pathway. , 1997, Genes & development.

[205]  W. Benedict,et al.  Expression of p16, Rb, and cyclin D1 gene products in oral and laryngeal squamous carcinoma: biological and clinical implications. , 1999, Human pathology.

[206]  K. Hemminki,et al.  Loss of heterozygosity at chromosome 9p21 (INK4-p14ARF locus): homozygous deletions and mutations in the p16 and p14ARF genes in sporadic primary melanomas. , 1999, Melanoma research.

[207]  A. Kaye,et al.  Homozygous deletions of the multiple tumor suppressor gene 1 in the progression of human astrocytomas. , 1995, Cancer research.

[208]  R. Miike,et al.  Aberrant methylation of p16INK4a in anatomic and gender-specific subtypes of sporadic colorectal cancer. , 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[209]  M. Bulyk,et al.  Loss of the p16INK4a and p15INK4b genes, as well as neighboring 9p21 markers, in sporadic melanoma. , 1996, Cancer research.

[210]  R. Reddel,et al.  Association of extended in vitro proliferative potential with loss of p16INK4 expression. , 1996, Oncogene.

[211]  G. Peters,et al.  Inhibitors of cyclin-dependent kinases induce features of replicative senescence in early passage human diploid fibroblasts , 1998, Current Biology.

[212]  D. Bostwick,et al.  Absence of p16/MTS1 gene mutations in human prostate cancer. , 1996, Carcinogenesis.

[213]  S. Tavtigian,et al.  Complex structure and regulation of the P16 (MTS1) locus. , 1995, Cancer research.

[214]  M. Matsuoka,et al.  Increasing methylation of the CDKN2A gene is associated with the progression of adult T-cell leukemia. , 2000, Cancer research.

[215]  C. D. Edwards,et al.  Reciprocal Rb inactivation and p16INK4 expression in primary lung cancers and cell lines. , 1995, Cancer research.

[216]  R. Haw,et al.  Evidence for the inactivation of multiple replicative lifespan genes in immortal human squamous cell carcinoma keratinocytes , 1997, Oncogene.

[217]  E. Ramsay,et al.  Cdkn2a, the cyclin-dependent kinase inhibitor encoding p16INK4a and p19ARF, is a candidate for the plasmacytoma susceptibility locus, Pctr1. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[218]  R. Fåhraeus,et al.  The p16INK4a tumour suppressor protein inhibits αvβ3 integrin‐mediated cell spreading on vitronectin by blocking PKC‐dependent localization of αvβ3 to focal contacts , 1999 .

[219]  R. Eeles,et al.  Genetic evidence in melanoma and bladder cancers that p16 and p53 function in separate pathways of tumor suppression. , 1995, The American journal of pathology.

[220]  K. Post,et al.  Frequent inactivation of the p16 gene in human pituitary tumors by gene methylation , 1997, Molecular carcinogenesis.

[221]  Seongyong Kim,et al.  Alterations of CDKN2 (MTS1/p16INK4A) gene in paraffin-embedded tumor tissues of human stomach, lung, cervix and liver cancers , 1998, Experimental & Molecular Medicine.

[222]  F. Kaye,et al.  Absence of p16INK4 protein is restricted to the subset of lung cancer lines that retains wildtype RB. , 1994, Oncogene.

[223]  E. Hovig,et al.  Homozygous deletion frequency and expression levels of the CDKN2 gene in human sarcomas--relationship to amplification and mRNA levels of CDK4 and CCND1. , 1995, British Journal of Cancer.

[224]  D. Dean,et al.  Active Transcriptional Repression by the Rb–E2F Complex Mediates G1 Arrest Triggered by p16INK4a, TGFβ, and Contact Inhibition , 1999, Cell.

[225]  D. Haber,et al.  Tumour-suppressor genes: evolving definitions in the genomic age , 1997, Nature Genetics.

[226]  K. Hemminki,et al.  Mutations in the CDKN2A ( p16INK4a ) gene in microdissected sporadic primary melanomas , 1998, International journal of cancer.

[227]  A. Iolascon,et al.  Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemias. , 1996, Leukemia.

[228]  D. Grandér,et al.  p15ink4B and p16ink4 gene inactivation in acute lymphocytic leukemia. , 1995, Blood.

[229]  Y. Fu,et al.  Association of K-ras mutations with p16 methylation in human colon cancer. , 1999, Gastroenterology.

[230]  S. Tsunoda,et al.  Alterations of retinoblastoma, p53, p16(CDKN2), and p15 genes in human astrocytomas , 1996, Cancer.

[231]  R. Beart,et al.  Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing. , 1995, Cancer research.

[232]  M. Rugge,et al.  p16/CDKN2 alterations and pRb expression in oesophageal squamous carcinoma. , 1998, Molecular pathology : MP.

[233]  N. Hayward,et al.  Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma , 1996, Nature Genetics.

[234]  Karen H. Vousden,et al.  p14ARF links the tumour suppressors RB and p53 , 1998, Nature.

[235]  P. Pollock,et al.  Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds , 1997, Oncogene.

[236]  T. Sano,et al.  Infrequent mutations of p16INK4A and p15INK4B genes in human pituitary adenomas. , 1997, European journal of endocrinology.

[237]  D. Louis,et al.  MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p. , 1994, Human molecular genetics.

[238]  K. Ichimura,et al.  Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours. , 1997, British journal of cancer.

[239]  Hsiu‐Po Wang,et al.  Intragenic Homozygous Deletions of MTS1 Gene in Gastric Cancer in Taiwan , 1996, Japanese journal of cancer research : Gann.

[240]  J. Fletcher,et al.  Codeletion of p15 and p16 genes in primary non-small cell lung carcinoma. , 1995, Cancer research.

[241]  Rudolf Jaenisch,et al.  Role for DNA methylation in genomic imprinting , 1993, Nature.

[242]  S. Chi,et al.  Mutational alteration of the p16CDKN2a tumor suppressor gene is infrequent in Ewing's sarcoma. , 1999, Oncology reports.

[243]  P. Goodfellow,et al.  Frequent mutations of CDKN2 in primary pancreatic adenocarcinomas , 1995, Genes, chromosomes & cancer.

[244]  N. Hayward,et al.  Low frequency of p16/CDKN2A methylation in sporadic melanoma: comparative approaches for methylation analysis of primary tumors. , 1997, Cancer research.

[245]  S. Rockman,et al.  Methylation of exon 2 of p16 is associated with late stage oesophageal cancer. , 2000, Cancer letters.

[246]  B. Tycko,et al.  MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme. , 1995, The American journal of pathology.

[247]  D. Quelle,et al.  Cancer-associated mutations at the INK4a locus cancel cell cycle arrest by p16INK4a but not by the alternative reading frame protein p19ARF. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[248]  R. Takahashi,et al.  Contribution of Chromosome 9p21‐22 Deletion to the Progression of Human Renal Cell Carcinoma , 1995, Japanese journal of cancer research : Gann.

[249]  T. Goodrow,et al.  Deletion and mutation analyses of the P16/MTS-1 tumor suppressor gene in human ductal pancreatic cancer reveals a higher frequency of abnormalities in tumor-derived cell lines than in primary ductal adenocarcinomas. , 1996, Cancer research.

[250]  C. Shields,et al.  Deletion mapping of chromosome region 9p21‐p22 surrounding the CDKN2 locus in melanoma , 1996, International journal of cancer.

[251]  T. Kinoshita,et al.  Mutational analysis of the CDKN2 (MTS1/p16ink4A) gene in primary B-cell lymphomas. , 1995, Blood.

[252]  W. Schulz,et al.  DNA Methylation and the Mechanisms of CDKN2A Inactivation in Transitional Cell Carcinoma of the Urinary Bladder , 2000, Laboratory Investigation.

[253]  D. Louis,et al.  Aberrations of the p53 pathway components p53, MDM2 and CDKN2A appear independent in diffuse large B cell lymphoma , 1999, Leukemia.

[254]  D. Sidransky,et al.  Role of the p16 tumor suppressor gene in cancer. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[255]  C. D. Edwards,et al.  A novel p16INK4A transcript. , 1995, Cancer research.

[256]  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.

[257]  M. Nistér,et al.  Induction of senescence in human malignant glioma cells by p16INK4A , 1997, Oncogene.