TY - JOUR
T1 - Anx7, a candidate tumor suppressor gene for prostate cancer
AU - Srivastava, Meera
AU - Bubendorf, Lukas
AU - Srikantan, Vasantha
AU - Fossom, Linda
AU - Nolan, Lisa
AU - Glasman, Mirta
AU - Leighton, Ximena
AU - Fehrle, Wilfred
AU - Pittaluga, Stefania
AU - Raffeld, Mark
AU - Koivisto, Pasi
AU - Willi, Niels
AU - Gasser, Thomas C.
AU - Kononen, Juha
AU - Sauter, Guido
AU - Kallioniemi, Olli P.
AU - Srivastava, Shiv
AU - Pollard, Harvey B.
PY - 2001/4/10
Y1 - 2001/4/10
N2 - 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 TSG, 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.
AB - 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 TSG, 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.
KW - Cancer genetics
KW - Chromosome 10q21
KW - Loss of heterozygosity
UR - http://www.scopus.com/inward/record.url?scp=0035836654&partnerID=8YFLogxK
U2 - 10.1073/pnas.071055798
DO - 10.1073/pnas.071055798
M3 - Article
C2 - 11287641
AN - SCOPUS:0035836654
SN - 0027-8424
VL - 98
SP - 4575
EP - 4580
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 8
ER -