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miR-135b在胃癌发生发展中的临床病理意义及功能

[Clinicopathological significance and function of miR-135b in the occurrence and development of gastric cancer].

作者信息

Wang Lin-pei, Ma Xiao-qiu, Cai Jian-chun

机构信息

Department of Surgical Oncology, Xiamen Cancer Center, First Affiliated Hospital, Xiamen University, Xiamen 361003, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2012 Dec 11;92(46):3269-73.

Abstract

OBJECTIVE

To explore the function and clinicopathological significance of miR-135b in the occurrence and development of gastric cancer.

METHODS

Seventy-two pairs of fresh gastric cancer tissues and corresponding normal gastric epithelium were collected at our department from September 2007 to March 2011. Six of them were randomly selected and miRNA microarray was applied to study the miRNA expression profiles of gastric cancer. Quantitative real-time PCR was used to validate the reliability of microarray and detect miR-135b expression in the above clinical samples, as well as cell lines GES-1, BGC-823 and SGC-7901. The methods of cell transfection, thiazolyl blue tetrazolium bromide (MTT) and flow cytometry were used to study the impact of miR-135 on cell proliferation, cell cycle and apoptosis of gastric cancer cells. Real-time quantitative PCR and Western blot were used to explore the relationship between miR-135b and adenomatous polyposis coli (APC).

RESULTS

Compared with normal gastric tissues, 7 miRNA were significantly up-regulated and 9 miRNA significantly down-regulated for over 2 folds in gastric cancer tissues (P < 0.05). The results of microarray were verified by quantitative real-time PCR. MiR-135b expression was up-regulated in most clinical samples compared with their corresponding epithelium (n = 66, 91.67%). The average expression level of miR-135b in gastric cancer tissues was significantly higher than normal epithelium (3.42 ± 2.62 vs 1.00 ± 0.07, P < 0.05). MiR-135b was related to Laurén classification, tumor differentiation, invasion and pathologic tumor-node-metastasis (pTNM) stage of gastric cancer (all P < 0.05). The worse differentiation degree of gastric cell lines, the higher miR-135b expression level (P < 0.05). MiR-135b promoted gastric cancer cell proliferation, inhibited its apoptosis and directly regulated the expression of APC in gastric cancer cell.

CONCLUSIONS

Special miRNA expression profiles of gastric cancer are found. MiR-135b is closely correlated with the biological behavior of human gastric cancer. And its regulation of APC may be one of the pathogenic mechanisms of gastric cancer.

摘要

目的

探讨miR-135b在胃癌发生发展中的作用及临床病理意义。

方法

收集2007年9月至2011年3月我院72对新鲜胃癌组织及相应正常胃黏膜上皮组织。随机选取其中6对,应用miRNA芯片研究胃癌组织的miRNA表达谱。采用定量实时荧光定量PCR验证芯片结果的可靠性,并检测上述临床样本及胃黏膜上皮细胞系GES-1、胃癌细胞系BGC-823和SGC-7901中miR-135b的表达。运用细胞转染、噻唑蓝比色法(MTT)及流式细胞术研究miR-135对胃癌细胞增殖、细胞周期及凋亡的影响。采用实时荧光定量PCR及蛋白质免疫印迹法探讨miR-135b与腺瘤性结肠息肉病蛋白(APC)的关系。

结果

与正常胃组织相比,胃癌组织中有7种miRNA显著上调、9种miRNA显著下调2倍以上(P<0.05)。定量实时荧光定量PCR验证了芯片结果。与相应正常上皮组织相比,多数临床样本中miR-135b表达上调(n=66,91.67%)。胃癌组织中miR-135b的平均表达水平显著高于正常上皮组织(3.42±2.62 vs 1.00±0.07,P<0.05)。miR-135b与胃癌的Laurén分型、肿瘤分化程度、浸润及病理分期(pTNM分期)相关(均P<0.05)。胃癌细胞系分化程度越差,miR-135b表达水平越高(P<0.05)。miR-135b促进胃癌细胞增殖,抑制其凋亡,并直接调控胃癌细胞中APC的表达。

结论

发现胃癌存在特异性miRNA表达谱。miR-135b与人胃癌生物学行为密切相关。其对APC的调控可能是胃癌发病机制之一。

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