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II型类固醇5α-还原酶TA重复序列多态性与澳大利亚女性患乳腺癌或卵巢癌的风险无关。

The steroid 5alpha-reductase type II TA repeat polymorphism is not associated with risk of breast or ovarian cancer in Australian women.

作者信息

Spurdle A B, Hopper J L, Chen X, Dite G S, McCredie M R, Giles G G, Venter D J, Southey M C, Purdie D M, Chenevix-Trench G

机构信息

Oncology Division, Joint Experimental Oncology Programme, The Queensland Institute of Medical Research, and The University of Queensland, Brisbane, QLD 4029 Australia.

出版信息

Cancer Epidemiol Biomarkers Prev. 2001 Dec;10(12):1287-93.

Abstract

The enzyme 5alpha-reductase type II (SRD5A2) converts testosterone to its more active form 5alpha-dihydroxytestosterone. The 3' untranslated region of the gene contains a (TA)(n) length polymorphism. The (TA)(9) allele has been reported to be associated with higher serum prostate-specific antigen levels in breast tumors and lower risk of relapse in breast cancer patients and more recently has also been reported to be linked to the codon 89 valine variant, which is itself associated with higher serum prostate-specific antigen levels in breast tumors and a more favorable breast cancer prognosis. We investigated whether the SRD5A2 (TA)(n) polymorphism was associated with risk of breast or ovarian cancer in Australian women by studying 946 breast cancer cases and 509 age-matched controls, and 544 ovarian cancer cases and 298 controls of similar age distribution. The (TA)(9) allele frequency was similar in breast cancer cases (0.110), breast cancer controls (0.125), ovarian cancer cases (0.106), and ovarian cancer controls (0.117). There was no difference in genotype distribution between breast cancer cases and controls (P = 0.5), ovarian cancer cases and controls (P = 0.7), or between the two control groups (P = 0.9). Genotypes containing at least one (TA)(9) allele were not significantly associated with risk of breast cancer overall (odds ratio, 0.86; 95% confidence interval, 0.67-1.12; P = 0.3) or in women stratified by age, menopausal status, or family history. Similarly, the (TA)(9) allele was not associated with risk of ovarian cancer (odds ratio, 0.87; 95% confidence interval, 0.61-1.23; P = 0.4) or with ovarian tumor behavior (invasive or low malignant potential), histology, stage, or grade. Given that this study had sufficient power to detect altered risks in the order of 1.4- to 1.7-fold, our results suggest that the SRD5A2 (TA)(9) allele is unlikely to be associated with moderate alterations in breast or ovarian cancer risk.

摘要

II型5α-还原酶(SRD5A2)可将睾酮转化为其活性更高的形式5α-二氢睾酮。该基因的3'非翻译区存在一个(TA)(n)长度多态性。据报道,(TA)(9)等位基因与乳腺肿瘤中较高的血清前列腺特异性抗原水平以及乳腺癌患者较低的复发风险相关,最近还报道其与密码子89缬氨酸变体有关,而该变体本身与乳腺肿瘤中较高的血清前列腺特异性抗原水平及更有利的乳腺癌预后相关。我们通过研究946例乳腺癌病例和509例年龄匹配的对照,以及544例卵巢癌病例和298例年龄分布相似的对照,调查了澳大利亚女性中SRD5A2(TA)(n)多态性与乳腺癌或卵巢癌风险是否相关。(TA)(9)等位基因频率在乳腺癌病例(0.110)、乳腺癌对照(0.125)、卵巢癌病例(0.106)和卵巢癌对照(0.117)中相似。乳腺癌病例与对照之间(P = 0.5)、卵巢癌病例与对照之间(P = 0.7)或两个对照组之间(P = 0.9)的基因型分布无差异。总体而言,含有至少一个(TA)(9)等位基因的基因型与乳腺癌风险无显著关联(优势比,0.86;95%置信区间,0.67 - 1.12;P = 0.3),在按年龄、绝经状态或家族史分层的女性中也是如此。同样,(TA)(9)等位基因与卵巢癌风险无关(优势比,0.87;95%置信区间,0.61 - 1.23;P = 0.4),也与卵巢肿瘤行为(侵袭性或低恶性潜能)、组织学、分期或分级无关。鉴于本研究有足够的能力检测出1.4至1.7倍左右的风险改变,我们的结果表明,SRD5A2(TA)(9)等位基因不太可能与乳腺癌或卵巢癌风险的中度改变相关。

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