ANX7, a candidate tumor suppressor gene for prostate cancer

被引:112
作者
Srivastava, M
Bubendorf, L
Srikantan, V
Fossom, L
Nolan, L
Glasman, M
Leighton, X
Fehrle, W
Pittaluga, S
Raffeld, M
Koivisto, P
Willi, N
Gasser, TC
Kononen, J
Sauter, G
Kallioniemi, OP
Srivastava, S
Pollard, HB
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Anat Physiol & Genet, Sch Med, Bethesda, MD 20814 USA
[2] Uniformed Serv Univ Hlth Sci, Inst Mol Med, Sch Med, Bethesda, MD 20814 USA
[3] Uniformed Serv Univ Hlth Sci, Ctr Prostate Dis Res, Sch Med, Bethesda, MD 20814 USA
[4] Uniformed Serv Univ Hlth Sci, Dept Surg, Sch Med, Bethesda, MD 20814 USA
[5] Natl Human Genome Res Inst, Canc Genet Branch, Sect Mol Genet, NIH, Bethesda, MD 20892 USA
[6] NCI, Pathol Lab, Hematopathol Sect, NIH, Bethesda, MD 20892 USA
[7] Tampere Univ Hosp, Canc Genet Lab, FIN-33520 Tampere, Finland
[8] Univ Basel, Inst Pathol, CH-4031 Basel, Switzerland
[9] Univ Basel, Urol Clin, CH-4031 Basel, Switzerland
关键词
cancer genetics; chromosome; 10q21; loss of heterozygosity;
D O I
10.1073/pnas.071055798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ANX7 gene is located on human chromosome 10q21, a site long hypothesized to harbor a tumor suppressor gene(s) (TSG) associated with prostate and other cancers. To test whether ANX7 might be a candidate TSC, we examined the ANX7-dependent suppression of human tumor cell growth, stage-specific ANX7 expression in 301 prostate specimens on a prostate tissue microarray, and loss of heterozygosity (LOH) of microsatellite markers at or near the ANX7 locus. Here we report that human tumor cell proliferation and colony formation are markedly reduced when the wild-type ANX7 gene is transfected into two prostate tumor cell lines, LNCaP and DU145. Consistently, analysis of ANX7 protein expression in human prostate tumor microarrays reveals a significantly higher rate of loss of ANX7 expression in metastatic and local recurrences of hormone refractory prostate cancer as compared with primary tumors (P = 0.0001). Using four microsatellite markers at or near the ANX7 locus, and laser capture microdissected tumor cells, 35% of the 20 primary prostate tumors show LOH. The microsatellite marker closest to the ANX7 locus showed the highest rate of LOH, including one homozygous deletion. We conclude that the ANX7 gene exhibits many biological and genetic properties expected of a TSG and may play a role in prostate cancer progression.
引用
收藏
页码:4575 / 4580
页数:6
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