Zhang Shanxin, Yuan Wei, Tang Wanyan, Xu Changqing, Ma Jie
Department of Gastroenterology, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan 250014, China.
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Zhonghua Zhong Liu Za Zhi. 2015 Aug;37(8):603-8.
The aim of this study was to investigate the expression of microRNA-100 (miR-100) and its relation with prognosis in colorectal cancer (CRC).
The expression of miR-100 was analyzed by quantitative real-time PCR (qRT-PCR) in 172 CRC tissue samples. The relation of miR-100 expression patterns with clinical pathological significance in CRC was analyzed. The effects of alterations of miR-100 expression and its consequences on CRC cell proliferation, apoptosis and migration were demonstrated in cells cultured in vitro.
The relative expression of miR-100 in CRC tissues and peritumoral tissues were -6.185 ± 1.921 and -3.698 ± 1.786, respectively, with a significant difference between the two groups (P<0.01). There was a significant difference between the relative expression of miR-100 in CRC with lymph node metastasis (-5.706 ± 1.809) and without lymph node metastasis (-6.775 ± 1.902, P<0.01). The relative expression of miR-100 in tumors of different TNM stages were -7.267 ± 1.888 in stage I, -6.443 ± 1.859 in stage II, -5.923 ± 1.796 in stage III, and -4.639 ± 1.516 in stage IV, with a significant difference among them (P<0.01). Different differentiation grades showed different expression of miR-100, i.e. -7.389 ± 1.828 in well differentiated tumors, -6.095 ± 1.843 in moderately differentiated tumors, and -5.476 ± 2.088 in poorly differentiated tumors (P<0.01). There was no significant correlation between miR-100 expression and overall survival rates of the CRC patients (P=0.179). Overexpression of miR-100 in the CRC cell line HCT-8 inhibited cell proliferation, but promoted cell apoptosis and migration.
The expression of miR-100 is correlated with lymph node metastasis, TNM stage and differentiation grade, and may be a potential biomarker indicating the development of CRC.
本研究旨在探讨微小RNA - 100(miR - 100)在结直肠癌(CRC)中的表达及其与预后的关系。
采用定量实时荧光定量PCR(qRT - PCR)分析172例CRC组织样本中miR - 100的表达。分析miR - 100表达模式与CRC临床病理意义的关系。在体外培养的细胞中证实miR - 100表达改变及其对CRC细胞增殖、凋亡和迁移的影响。
CRC组织和癌旁组织中miR - 100的相对表达分别为-6.185±1.921和-3.698±1.786,两组间差异有统计学意义(P<0.01)。有淋巴结转移的CRC中miR - 100的相对表达(-5.706±1.809)与无淋巴结转移的CRC(-6.775±1.902,P<0.01)之间存在显著差异。不同TNM分期肿瘤中miR - 100的相对表达在I期为-7.267±1.888,II期为-6.443±1.859,III期为-5.923±1.796,IV期为-4.639±1.516,差异有统计学意义(P<0.01)。不同分化程度显示miR - 100表达不同,即高分化肿瘤中为-7.389±1.828,中分化肿瘤中为-6.095±1.843,低分化肿瘤中为-5.476±2.088(P<0.01)。miR - 100表达与CRC患者的总生存率无显著相关性(P = 0.179)。在CRC细胞系HCT - 8中过表达miR - 100可抑制细胞增殖,但促进细胞凋亡和迁移。
miR - 100的表达与淋巴结转移、TNM分期和分化程度相关,可能是指示CRC发生发展的潜在生物标志物。