CDKN2A (p16(INK4A)) somatic and germline mutations

被引:0
|
作者
SmithSorensen, B
Hovig, E
机构
[1] NORWEGIAN RADIUM HOSP,INST CANC RES,DEPT GENET,N-0310 OSLO,NORWAY
[2] NORWEGIAN RADIUM HOSP,INST CANC RES,DEPT TUMOR BIOL,N-0310 OSLO,NORWAY
关键词
CDKN2A gene; database; proteins;
D O I
10.1002/(SICI)1098-1004(1996)7:4<294::AID-HUMU2>3.0.CO;2-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The cell cycle is composed of a series of steps that can be negatively or positively regulated by various factors. A group of low-molecular-weight proteins have recently been identified that specifically inhibit the function of cyclin dependent kinases in mammalian cells. Inactivation of the CDKN2A gene (also known as p16(INK4A) and MTS1) attracted considerable interest after it was mapped to 9p21, a locus for familial melanoma. In an effort to standardize the information regarding human CDKN2A mutations detected in cancers, a database with information of 146 point mutations has been created. Cancer type, origin of cells, specific mutation, amino acid change, literature citation, and other data are provided for each mutation entry. Studies of biochemical and biological functions of both wild-type and mutant proteins are central to our understanding of the role of p16(INK4a) mutations in tumorigenesis, a summary of these studies is also included in the present update. (C) 1996 Wiley Liss, Inc.
引用
收藏
页码:294 / 303
页数:10
相关论文
共 50 条
  • [11] Differential expression of p16(INK4a) and p16 beta transcripts in B-lymphoblastoid cells from members of hereditary melanoma families without CDKN2A exon mutations
    Rizos, H
    Becker, TM
    Holland, EA
    Kefford, RF
    Mann, GJ
    ONCOGENE, 1997, 15 (05) : 515 - 523
  • [12] p16(MTS-1/CDKN2/INK4a) in cancer progression
    Rocco, JW
    Sidransky, D
    EXPERIMENTAL CELL RESEARCH, 2001, 264 (01) : 42 - 55
  • [13] p16(INK4a) and pl9(ARF) germline mutations in familial melanoma.
    Fargnoli, MC
    Chimenti, S
    Keller, G
    DalPozzo, V
    Soyer, P
    Hofler, H
    Peris, K
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1997, 109 (03) : 424 - 424
  • [14] Human glioblastomas with no alterations of the CDKN2A (p16(INK4A), MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene
    Ichimura, K
    Schmidt, EE
    Goike, HM
    Collins, VP
    ONCOGENE, 1996, 13 (05) : 1065 - 1072
  • [15] CDKN2A/p16 in ependymomas
    Simona Bortolotto
    Loredana Chiadò-Piat
    Paola Cavalla
    Ivana Bosone
    Alessandro Mauro
    Davide Schiffer
    Journal of Neuro-Oncology, 2001, 54 : 9 - 13
  • [16] CDKN2A/p16 in ependymomas
    Bortolotto, S
    Chiadò-Piat, L
    Cavalla, P
    Bosone, I
    Mauro, A
    Schiffer, D
    JOURNAL OF NEURO-ONCOLOGY, 2001, 54 (01) : 9 - 13
  • [17] Association of CDKN2A/p16(INK4A) with human head and neck keratinocyte replicative senescence: Relationship of dysfunction to immortality and neoplasia
    Loughran, O
    Malliri, A
    Owens, D
    Gallimore, PH
    Stanley, MA
    Ozanne, B
    Frame, MC
    Parkinson, EK
    ONCOGENE, 1996, 13 (03) : 561 - 568
  • [18] p16(INK4A)/MTS1/CDKN2 - The melanoma gene? [p16(INK4A)/MTS1/CDKN2 das'melanomgen'? Stand der forschung und ausblick]
    Bogenrieder T.
    Landthaler M.
    Stolz W.
    Der Hautarzt, 1998, 49 (2): : 91 - 100
  • [19] No mutations found in the exon 2 of p16 INK4a and K-ras
    Minicucci, E. M.
    Silva, G. N.
    Ribeiro, D. A.
    Salvadori, D. M. F.
    ORAL ONCOLOGY, 2009, : 217 - 217
  • [20] A NOVEL P16(INK4A) TRANSCRIPT
    MAO, L
    MERLO, A
    BEDI, G
    SHAPIRO, GI
    EDWARDS, CD
    ROLLINS, BJ
    SIDRANSKY, D
    CANCER RESEARCH, 1995, 55 (14) : 2995 - 2997