Deletion of a small consensus region at 6q15, including the MAP3K7 gene, is significantly associated with high-grade prostate cancers

被引:54
作者
Liu, Wennuan
Chang, Bao-Li
Cramer, Scott
Koty, Patrick P.
Li, Tao
Sun, Jishan
Turner, Aubrey R.
Kap-Herr, ChrisVon
Bobb, Peggy
Rao, Jianyu
Zheng, S. Lilly
Isaacs, William B.
Xu, Jianfeng
机构
[1] Johns Hopkins Med Inst, Dept Urol, Baltimore, MD 21287 USA
[2] Wake Forest Univ, Sch Med, Ctr Human Genome, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Sch Med, Dept Canc Biol, Winston Salem, NC 27109 USA
[4] Wake Forest Univ, Sch Med, Dept Pediat, Winston Salem, NC 27109 USA
[5] Univ Calif Los Angeles, Dept Pathol, Los Angeles, CA 90024 USA
关键词
D O I
10.1158/1078-0432.CCR-07-0300
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Chromosome 6q14-21 is commonly deleted in prostate cancers, occurring in similar to 22% of all tumors and similar to 40% of metastatic tumors. However, candidate prostate tumor suppressor genes in this region have not been identified, in part due to the large and broad nature of the deleted region implicated in previous studies. Experimental Design:We first used high-resolution Affymetrix single nucleoticle polymorphism arrays to examine DNA from malignant and matched nonmalignant cells from 55 prostate cancer patients. We identified a small consensus region on 6q14-21 and evaluated the deletion status within the region among additional 40 tumors and normal pairs using quantitative PCR and fluorescence in situ hybridization. We finally tested the association between the deletion and Gleason score using the Fisher's exact test. Results: Tumors with small, interstitial deletions at 6q14-21 defined an 817-kb consensus region that is affected in 20 of 21 tumors. The MAP3K7 gene is one of five genes located in this region. In total, MAP3K7 was deleted in 32% of 95 tumors. Importantly, deletion of MAP3K7 was highly associated with higher-grade disease, occurring in 61% of tumors with Gleason score,: 8 compared with only 22% of tumors with Gleason score : T The difference was highly significant (P = 0.001). Conclusion: Our study provides strong evidence for the first time that a small deletion at 6q15, including the MAP3K7 gene and four other genes, is associated with high-grade prostate cancers. Although the deletion may be a marker for high-grade prostate cancer, additional studies are needed to understand its molecular mechanisms.
引用
收藏
页码:5028 / 5033
页数:6
相关论文
共 14 条
[1]   TGF-β and cancer [J].
Bierie, B ;
Moses, HL .
CYTOKINE & GROWTH FACTOR REVIEWS, 2006, 17 (1-2) :29-40
[2]   Physical mapping of chromosome 8p22 markers and their homozygous deletion in a metastatic prostate cancer [J].
Bova, GS ;
MacGrogan, D ;
Levy, A ;
Pin, SS ;
Bookstein, R ;
Isaacs, WB .
GENOMICS, 1996, 35 (01) :46-54
[3]  
Cooney KA, 1996, CANCER RES, V56, P4150
[4]   Chromosomal deletions and tumor suppressor genes in prostate cancer [J].
Dong, JT .
CANCER AND METASTASIS REVIEWS, 2001, 20 (3-4) :173-193
[5]   Defining the region(s) of deletion at 6q16-q22 in human prostate cancer [J].
Hyytinen, ER ;
Saadut, R ;
Chen, CS ;
Paull, L ;
Koivisto, PA ;
Vessella, RL ;
Frierson, HF ;
Dong, JT .
GENES CHROMOSOMES & CANCER, 2002, 34 (03) :306-312
[6]   Genetic mapping of allelic loss on chromosome 6q within heterogeneous prostate carcinoma [J].
Konishi, N ;
Nakamura, M ;
Kishi, M ;
Ishida, E ;
Shimada, K ;
Matsuyoshi, S ;
Nagai, H ;
Emi, M .
CANCER SCIENCE, 2003, 94 (09) :764-768
[7]   dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data [J].
Lin, M ;
Wei, LJ ;
Sellers, WR ;
Lieberfarb, M ;
Wong, WH ;
Li, C .
BIOINFORMATICS, 2004, 20 (08) :1233-1240
[8]   Comprehensive assessment of DNA copy number alterations in human prostate cancers using Affymetrix 100K SNP mapping array [J].
Liu, Wennuan ;
Chang, Baoli ;
Sauvageot, Jurga ;
Dimitrov, Latchezar ;
Gielzak, Marta ;
Li, Tao ;
Yan, Guifang ;
Sun, Jishan ;
Sun, Jielin ;
Adams, Tamara S. ;
Turner, Aubrey R. ;
Kim, Jin Woo ;
Meyers, Deborah A. ;
Zheng, Siqun Lilly ;
Isaacs, William B. ;
Xu, Jianfeng .
GENES CHROMOSOMES & CANCER, 2006, 45 (11) :1018-1032
[9]   Representational oligonucleotide microarray analysis: A high-resolution method to detect genome copy number variation [J].
Lucito, R ;
Healy, J ;
Alexander, J ;
Reiner, A ;
Esposito, D ;
Chi, MY ;
Rodgers, L ;
Brady, A ;
Sebat, J ;
Troge, J ;
West, JA ;
Rostan, S ;
Nguyen, KCQ ;
Powers, S ;
Ye, KQ ;
Olshen, A ;
Venkatraman, E ;
Norton, L ;
Wigler, M .
GENOME RESEARCH, 2003, 13 (10) :2291-2305
[10]   A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays [J].
Nannya, Y ;
Sanada, M ;
Nakazaki, K ;
Hosoya, N ;
Wang, LL ;
Hangaishi, A ;
Kurokawa, M ;
Chiba, S ;
Bailey, DK ;
Kennedy, GC ;
Ogawa, S .
CANCER RESEARCH, 2005, 65 (14) :6071-6079