microrna调节结直肠癌患者的生存素

Mortaza Raeisi, Hadi Chavoshi, Soghra Bornehdeli, Milad Asadi, Roya Dolatkhah, Ayse Caner
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摘要

背景:肿瘤细胞存活率的降低与肿瘤细胞存活率的增加有关。在这项研究中,我们打算分析伊朗结直肠癌(CRC)患者肿瘤和边缘组织中靶向survivin的microrna (miRNAs)。材料与方法:招募50例伊朗阿扎里族结直肠癌患者。分离肿瘤和边缘组织的RNA含量,通过定量Real-time PCR检测miR-34a、miR-16、miR-150、miR-203a和survivin的转录物水平。结果:survivin mRNA在肿瘤组织中的表达明显高于边缘组织(fold change = 3.21, P = 0.0029)。与边缘样本相比,肿瘤样本中miR-16 (fold change = 0.28, P = 0.003)和miR-203a (fold change = 0.36, P = 0.014)的表达明显下调。两者呈显著负相关(rho = -0.81;P < 0.001),在结直肠癌患者肿瘤组织中miR-203a的表达与survivin mRNA的表达之间存在显著性差异。survivin mRNA在有淋巴结转移的结直肠癌患者肿瘤组织中的表达明显高于无淋巴结转移的结直肠癌患者(P = 0.020)。此外,有淋巴结转移的结直肠癌患者肿瘤组织中miR-203的表达水平明显高于无淋巴结转移的结直肠癌患者(P = 0.011)。结论:提示miR-203通过调控survivin和淋巴结转移在结直肠癌中起致瘤作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
microRNAs regulate survivin in colorectal cancer patients
Background: Impaired levels of surviving are associate with increased survival of tumor cells. In this study, we intended to profile the microRNAs (miRNAs) targeting survivin in the tumoral and marginal tissues obtained from Iranian patients with colorectal cancer (CRC).Materials and Methods: Fifty CRC patients of Iranian Azari ethnicity were recruited. The RNA content of the tumoral and marginal tissues was isolated and the transcript levels of miR-34a, miR-16, miR-150, and miR-203a and survivin were determined through quantitative Real-time PCR.Results: The mRNA expression of survivin was significantly increased (fold change = 3.21, P = 0.0029) in the tumoral tissues in comparison to the marginal tissues. There was significant downregulation of miR-16 (fold change = 0.28, P = 0.003) and miR-203a (fold change = 0.36, P = 0.014) in the tumoral samples in comparison to marginal samples. There was an inverse significant correlation (rho = -0.81; P < 0.001) between the expression of miR-203a and mRNA expression of survivin in the tumoral tissues of CRC patients. The mRNA expression of survivin was higher significantly in the tumoral tissues of CRC patients with lymph node metastasis in comparison to those without lymph node metastasis (P = 0.020). In addition, there was a significantly higher miR-203 expression level in the tumoral tissues of CRC patients with lymph node metastasis in comparison to those without lymph node metastasis (P = 0.011).Conclusion: It is suggested that miR-203 plays an oncogenic role in CRC cancer by regulating survivin and lymph node metastasis.
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