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A gender specific improved survival related to stromal miR-143 and miR-145 expression in non-small cell lung cancer

机译:非小细胞肺癌中与基质miR-143和miR-145表达相关的性别特异性生存改善

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Micro RNAs (miRNA) are small non-coding RNAs that post-transcriptionally regulate gene expression. Dysregulation of miRNA cluster 143/145 has been reported in several malignancies, but their role in non-small cell lung cancer (NSCLC) remains elusive. This study investigates the prognostic impact of miR-143 and miR-145 in primary tumors and metastatic lymph nodes in NSCLC tissue. Tissue from 553 primary tumors and 143 matched metastatic lymph nodes were collected and tissue microarrays were constructed. In situ hybridization was used to evaluate miR-143 and miR-145 expression in tumor epithelial cells and stromal cells in the primary tumors and lymph nodes. In vivo data was supplemented with functional studies of cell lines in vitro to evaluate the role of miR-143 and miR-145 in NSCLC tumorigenesis. In our cohort, stromal miR-143 (S-miR-143) and miR-145 (S-miR-145) expression in primary tumor tissue were independent prognosticators of improved disease-specific survival (DSS) in female (S-miR-143, HR: 0.53, p?=?0.019) and male patients (S-miR-145, HR: 0.58, p?=?0.021), respectively. Interesting correlations between the miR cluster 143/145 and previously investigated steroid hormone receptors from the same cohort were identified, substantiating their gender dependent significance.
机译:微小RNA(miRNA)是小的非编码RNA,可在转录后调节基因表达。在多种恶性肿瘤中均已报道了miRNA簇143/145的失调,但其在非小细胞肺癌(NSCLC)中的作用仍然难以捉摸。这项研究调查了miR-143和miR-145对原发性肿瘤和NSCLC组织转移淋巴结的预后影响。收集来自553例原发性肿瘤和143个匹配的转移性淋巴结的组织,并构建组织微阵列。原位杂交用于评估原发肿瘤和淋巴结中肿瘤上皮细胞和基质细胞中miR-143和miR-145的表达。体内数据补充了体外细胞系的功能研究,以评估miR-143和miR-145在NSCLC肿瘤发生中的作用。在我们的队列中,原发性肿瘤组织中的基质miR-143(S-miR-143)和miR-145(S-miR-145)表达是女性(S-miR-S)疾病特异性生存率(DSS)改善的独立预后因子。分别为143,HR:0.53,p≤0.019)和男性患者(S-miR-145,HR:0.58,p≤0.021)。确定了miR簇143/145与先前研究的同一队列中的类固醇激素受体之间有趣的相关性,证实了它们的性别依赖性。

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