The meaning of p16ink4a expression in tumors Functional significance, clinical associations and future developments

被引:230
作者
Witkiewicz, Agnieszka K. [1 ,3 ]
Knudsen, Karen E. [1 ,2 ,4 ,5 ]
Dicker, Adam P. [1 ,5 ]
Knudsen, Erik S. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Cell & Canc Biol, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Dept Pathol, Philadelphia, PA 19107 USA
[4] Thomas Jefferson Univ, Dept Urol, Philadelphia, PA 19107 USA
[5] Thomas Jefferson Univ, Dept Radiat Oncol, Philadelphia, PA 19107 USA
关键词
RB; p16; CDKN2a; E2F; CDK; cyclin; therapy; radiation; CYCLIN-DEPENDENT KINASES; CELL LUNG-CANCER; HUMAN-PAPILLOMAVIRUS; PROSTATE-CANCER; SUPPRESSOR GENE; INHIBITION; SENESCENCE; PROTEIN; RB; P16;
D O I
10.4161/cc.10.15.16776
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The CDKN2A gene is a tumor suppressor that encodes the CDK4/6 inhibitor p16(ink4a). Loss of this tumor suppressor contributes to the bypass of critical senescent signals and is associated with progression to malignant disease. However, the high-level expression of p16(ink4a) in tumors is associated with aggressive subtypes of disease, and in certain clinical settings elevated p16(ink4a) expression is an important determinant for disease prognosis and therapeutic response. These seemingly contradictory facets of p16(ink4a) expression have lead to confusion related to the meaning of this tumor suppression in tumor pathobiology. As reviewed here, the alternative expression of p16(ink4a) represents an ideal marker for considering RB-pathway function, tumor heterogeneity and novel means for directing therapy.
引用
收藏
页码:2497 / 2503
页数:7
相关论文
共 62 条
[41]   Retinoblastoma protein partners [J].
Morris, EJ ;
Dyson, NN .
ADVANCES IN CANCER RESEARCH, VOL 82, 2001, 82 :1-54
[42]   COMPLEX-FORMATION OF HUMAN PAPILLOMAVIRUS-E7 PROTEINS WITH THE RETINOBLASTOMA TUMOR SUPPRESSOR GENE-PRODUCT [J].
MUNGER, K ;
WERNESS, BA ;
DYSON, N ;
PHELPS, WC ;
HARLOW, E ;
HOWLEY, PM .
EMBO JOURNAL, 1989, 8 (13) :4099-4105
[43]   DELETIONS OF THE CYCLIN-DEPENDENT KINASE-4 INHIBITOR GENE IN MULTIPLE HUMAN CANCERS [J].
NOBORI, T ;
MIURA, K ;
WU, DJ ;
LOIS, A ;
TAKABAYASHI, K ;
CARSON, DA .
NATURE, 1994, 368 (6473) :753-756
[44]  
OTTERSON GA, 1994, ONCOGENE, V9, P3375
[45]   Role of the CDKN2A locus in patients with multiple primary melanomas [J].
Puig, S ;
Malvehy, J ;
Badenas, C ;
Ruiz, A ;
Jimenez, D ;
Cuellar, F ;
Azon, A ;
Gonzàlez, U ;
Castel, T ;
Campoy, A ;
Herrero, J ;
Martí, R ;
Brunet-Vidal, J ;
Milà, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (13) :3043-3051
[46]   MUTATIONS ASSOCIATED WITH FAMILIAL MELANOMA IMPAIR P16(INK4) FUNCTION [J].
RANADE, K ;
HUSSUSSIAN, CJ ;
SIKORSKI, RS ;
VARMUS, HE ;
GOLDSTEIN, AM ;
TUCKER, MA ;
SERRANO, M ;
HANNON, GJ ;
BEACH, D ;
DRACOPOLI, NC .
NATURE GENETICS, 1995, 10 (01) :114-116
[47]   p16INK4A is a robust in vivo biomarker of cellular aging in human skin [J].
Ressler, Sigrun ;
Bartkova, Jirina ;
Niederegger, Harald ;
Bartek, Jiri ;
Scharffetter-Kochanek, Karin ;
Jansen-Duerr, Pidder ;
Wlaschek, Meinhard .
AGING CELL, 2006, 5 (05) :379-389
[48]   Prognostic Significance of p16INK4A and Human Papillomavirus in Patients With Oropharyngeal Cancer Treated on TROG 02.02 Phase III Trial [J].
Rischin, Danny ;
Young, Richard J. ;
Fisher, Richard ;
Fox, Stephen B. ;
Le, Quynh-Thu ;
Peters, Lester J. ;
Solomon, Ben ;
Choi, Jimin ;
O'Sullivan, Brian ;
Kenny, Lizbeth M. ;
McArthur, Grant A. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (27) :4142-4148
[49]  
RIVADENEIRA DB, PROLIFERATIVE SUPPRE
[50]   Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a [J].
Russo, AA ;
Tong, L ;
Lee, JO ;
Jeffrey, PD ;
Pavletich, NP .
NATURE, 1998, 395 (6699) :237-243