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ARID1A 基因表达降低与原发性胃癌预后不良相关。

Decreased expression of the ARID1A gene is associated with poor prognosis in primary gastric cancer.

机构信息

State Key Laboratory of Oncology in Southern China and Department of Experimental Research, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.

出版信息

PLoS One. 2012;7(7):e40364. doi: 10.1371/journal.pone.0040364. Epub 2012 Jul 13.

Abstract

BACKGROUND

The ARID1A gene encodes adenine-thymine (AT)-rich interactive domain-containing protein 1A, which participates in chromatin remodeling. ARID1A has been showed to function as a tumor suppressor in various cancer types. In the current study, we investigated the expression and prognosis value of ARID1A in primary gastric cancer. Meanwhile, the biological role of ARID1A was further investigated using cell model in vitro.

METHODOLOGY/PRINCIPAL FINDINGS: To investigate the role of ARID1A gene in primary gastric cancer pathogenesis, real-time quantitative PCR and western blotting were used to examine the ARID1A expression in paired cancerous and noncancerous tissues. Results revealed decreased ARID1A mRNA (P = 0.0029) and protein (P = 0.0015) expression in most tumor-bearing tissues compared with the matched adjacent non-tumor tissues, and in gastric cancer cell lines. To further investigate the clinicopathological and prognostic roles of ARID1A expression, we performed immunohistochemical analyses of the 224 paraffin-embedded gastric cancer tissue blocks. Data revealed that the loss of ARID1A expression was significantly correlated with T stage (P = 0.001) and grade (P = 0.006). Consistent with these results, we found that loss of ARID1A expression was significantly correlated with poor survival in gastric cancer patients (P = 0.003). Cox regression analyses showed that ARID1A expression was an independent predictor of overall survival (P = 0.029). Furthermore, the functions of ARID1A in the proliferation and colony formation of gastric cell lines were analyzed by transfecting cells with full-length ARID1A expression vector or siRNA targeting ARID1A. Restoring ARID1A expression in gastric cancer cells significantly inhibited cell proliferation and colony formation. Silencing ARID1A expression in gastric epithelial cell line significantly enhanced cell growth rate.

CONCLUSIONS/SIGNIFICANCE: Our data suggest that ARID1A may play an important role in gastric cancer and may serve as a valuable prognostic marker and potential target for gene therapy in the treatment of gastric cancer.

摘要

背景

ARID1A 基因编码富含腺嘌呤-胸腺嘧啶(AT)的相互作用域蛋白 1A,参与染色质重塑。ARID1A 已被证明在多种癌症类型中作为肿瘤抑制因子发挥作用。在本研究中,我们研究了 ARID1A 在原发性胃癌中的表达和预后价值。同时,我们还通过体外细胞模型进一步研究了 ARID1A 的生物学作用。

方法/主要发现:为了研究 ARID1A 基因在原发性胃癌发病机制中的作用,我们使用实时定量 PCR 和 Western blot 检测了配对的癌组织和非癌组织中 ARID1A 的表达。结果显示,与匹配的相邻非肿瘤组织相比,大多数肿瘤组织中 ARID1A mRNA(P = 0.0029)和蛋白(P = 0.0015)表达降低,并且在胃癌细胞系中也是如此。为了进一步研究 ARID1A 表达的临床病理和预后作用,我们对 224 例胃癌石蜡包埋组织块进行了免疫组织化学分析。数据显示,ARID1A 表达缺失与 T 分期(P = 0.001)和分级(P = 0.006)显著相关。与这些结果一致,我们发现 ARID1A 表达缺失与胃癌患者的不良生存显著相关(P = 0.003)。Cox 回归分析显示,ARID1A 表达是总生存的独立预测因子(P = 0.029)。此外,我们通过转染全长 ARID1A 表达载体或靶向 ARID1A 的 siRNA 转染细胞,分析了 ARID1A 在胃癌细胞系中的增殖和集落形成功能。在胃癌细胞中恢复 ARID1A 表达显著抑制了细胞增殖和集落形成。在胃上皮细胞系中沉默 ARID1A 表达显著增强了细胞生长速度。

结论/意义:我们的数据表明,ARID1A 可能在胃癌中发挥重要作用,并可能作为有价值的预后标志物和胃癌基因治疗的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8d/3396657/a8700c6e9dde/pone.0040364.g001.jpg

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