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AS3的基因组和表达改变与食管鳞状细胞癌的相关性。

Correlation of genomic and expression alterations of AS3 with esophageal squamous cell carcinoma.

作者信息

Zhang Yu, Huang Xiaoping, Qi Jun, Yan Cai, Xu Xin, Han Yaling, Wang Mingrong

机构信息

State Key Laboratory of Molecular Oncology, Cancer Institute/Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China.

出版信息

J Genet Genomics. 2008 May;35(5):267-71. doi: 10.1016/S1673-8527(08)60038-7.

Abstract

Androgen-induced proliferation shutoff gene AS3, also known as APRIN, is a growth inhibitory gene that is initially implicated in prostate cancer. This gene is required for androgen-dependent growth arrest and is a primary target for 1,25(OH)(2)D(3) and androgens. Allelic loss at AS3 locus has been linked to a variety of cancers. However, the correlation of genomic and expression alterations of AS3 with esophageal squamous cell carcinoma (ESCC) is not well established. In this study, the genomic and expression alterations of AS3 in ESCC and their clinical significance are evaluated. Loss of heterozygosity (LOH) analysis using an AS3 intragenic microsatellite marker D13S171 revealed 72% allelic loss at AS3 locus in ESCC, which is significantly correlated with higher pathological grade (P=0.042). RT-PCR examination showed that AS3 mRNA obviously decreased in 44% tumors and its down-regulation was correlated with the sex of patients (P=0.03). Furthermore, the correlation between genomic and expression alterations of AS3 gene was analyzed in 18 ESCC specimens, which indicated that the consistency between allelic loss and decreased mRNA expression of AS3 was relatively poor. The results of this study indicate that the aberrant expression of AS3 may be involved in the tumorigenesis of esophagus and is responsible for the male predominance of ESCC.

摘要

雄激素诱导的增殖阻断基因AS3,也称为APRIN,是一种最初与前列腺癌相关的生长抑制基因。该基因是雄激素依赖性生长停滞所必需的,并且是1,25(OH)₂D₃和雄激素的主要作用靶点。AS3基因座的等位基因缺失与多种癌症有关。然而,AS3的基因组和表达改变与食管鳞状细胞癌(ESCC)之间的相关性尚未明确。在本研究中,评估了ESCC中AS3的基因组和表达改变及其临床意义。使用AS3基因内微卫星标记D13S171进行杂合性缺失(LOH)分析显示,ESCC中AS3基因座的等位基因缺失率为72%,这与更高的病理分级显著相关(P = 0.042)。逆转录-聚合酶链反应(RT-PCR)检测显示,44%的肿瘤中AS3 mRNA明显降低,其下调与患者性别相关(P = 0.03)。此外,在18例ESCC标本中分析了AS3基因的基因组和表达改变之间的相关性,结果表明AS3的等位基因缺失与mRNA表达降低之间的一致性相对较差。本研究结果表明,AS3的异常表达可能参与了食管癌的发生,并导致了ESCC的男性优势。

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