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The Expression and Prognostic Significance of Claudin-8 and Androgen Receptor in Breast Cancer

机译:克劳丁-8和雄激素受体在乳腺癌中的表达及预后意义

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Purpose: Claudin-8 (CLDN8) has been identified as an androgen-regulated gene in prostate cancer. However, the role of CLDN8 has not been fully explored in breast cancer. We aimed to explore the expression of CLDN8 and androgen receptor (AR), determine the correlation between CLDN8 and AR, assess the prognostic value of CLDN8 and AR co-expression, and investigate the possible CLDN8 expression molecular mechanism in breast cancer. Materials and Methods: Twenty-eight pairs of fresh tumor tissues and adjacent noncancerous tissues were evaluated by Western blot for CLDN8. Then, 142 breast cancer samples were determined by immunohistochemistry for CLDN8 and AR. The association of clinicopathological features with CLDN8, AR and CLDN8, and AR co-expression was examined. The Cancer Genome Atlas (TCGA) was used to demonstrate the expression of CLDN8 and correlation between CLDN8 and AR. Kaplan–Meier survival analysis was performed to assess the prognostic impact of CLDN8 and AR co-expression. The mechanisms related to CLDN8 expression in breast cancer were explored by Gene Set Enrichment Analysis (GSEA). Results: CLDN8 was downregulated in breast cancer tissues and positively correlated with none lymph node metastasis ( P =0.016), low histological grade ( P =0.006), positive ER ( P =0.014), positive PR ( P =0.003), low Ki-67 index ( P =0.017) and molecular subtypes ( P =0.012). CLDN8 level was significantly associated with AR level (r=0.348; P 0.001). CLDN8 and AR co-expression was positively correlated with none lymph node metastasis ( P =0.007), low histological grade ( P =0.017), positive ER ( P =0.019), positive PR ( P =0.015) and low Ki-67 index group ( P =0.038). CLDN8 and AR co-expression had a better clinical prognosis. Conclusion: The expression of CLDN8 is directly related to the expression of AR. CLDN8 and AR co-expression might be a potential prognostic evaluation factor for breast cancer patients.
机译:目的:克劳丁-8(CLDN8)已被鉴定为前列腺癌中的雄激素调节基因。然而,CLDN8的作用尚未在乳腺癌中得到充分探索。我们旨在探讨CLDN8和雄激素受体(AR)的表达,确定CLDN8和AR之间的相关性,评估CLDN8和AR共同表达的预后值,并研究乳腺癌中可能的CLDN8表达分子机制。材料和方法:通过Western印迹对CLDN8的蛋白质印迹评估二十八对新鲜肿瘤组织和相邻的非癌组织。然后,通过免疫组织化学来确定142个乳腺癌样品用于CLDN8和Ar。研究了CLDN8,Ar和CldN8和Ar共表达的临床病理学特征的关联。使用癌症基因组Atlas(TCGA)来证明CLDN8的表达和CLDN8和AR之间的相关性。进行Kaplan-Meier存活分析,以评估CLDN8和AR共表达的预后影响。基因设定富集分析(GSEA)探索了与乳腺癌中CLDN8表达的机制。结果:CLDN8在乳腺癌组织中下调,与无淋巴结转移呈正相关(P = 0.016),低组织学等级(P = 0.006),正静脉(P = 0.014),阳性Pr(p = 0.003),低ki -67指数(P = 0.017)和分子亚型(P = 0.012)。 CLDN8水平与AR水平显着相关(r = 0.348; p <0.001)。 CLDN8和Ar CO-DEPIT表达与无淋巴结转移呈正相关(P = 0.007),低组织学等级(P = 0.017),正ER(P = 0.019),阳性PR(P = 0.015)和低ki-67指数组(P = 0.038)。 CLDN8和AR共同表达具有更好的临床预后。结论:CLDN8的表达与AR的表达直接相关。 CLDN8和Ar共表达可能是乳腺癌患者的潜在预后评价因素。

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