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长链非编码 RNA LINC00973 的表达在结肠癌细胞用不同化疗药物处理后一致增加。

Expression of long non-coding RNA LINC00973 is consistently increased upon treatment of colon cancer cells with different chemotherapeutic drugs.

机构信息

Engelhardt Institute of Molecular Biology, The Russian Academy of Sciences, 119991, Moscow, Russia.

Engelhardt Institute of Molecular Biology, The Russian Academy of Sciences, 119991, Moscow, Russia; Institute of Biomedical Chemistry, The Russian Academy of Sciences, 119121, Moscow, Russia.

出版信息

Biochimie. 2018 Aug;151:67-72. doi: 10.1016/j.biochi.2018.05.021. Epub 2018 Jun 2.

Abstract

Early prediction of tumor relapse depends on the identification of new prognostic cancer biomarkers, which are suitable for monitoring tumor response to different chemotherapeutic drugs. Using RNA-Seq, RT-qPCR, bioinformatics, and studies utilizing the murine tumor xenograft model, we have found significant and consistent changes in the abundance of five lincRNAs (LINC00973, LINC00941, CASC19, CCAT1, and BCAR4) upon treatment of both HT-29 and HCT-116 cells with 5-fluorouracil, oxaliplatin, and irinotecan at different doses and durations; both in vitro and in vivo. The most frequent changes were detected for LINC00973, whose content is most strongly and consistently increased upon treatment of both colon cancer cell lines with all three chemotherapeutic drugs. Additional studies are required in order to determine the molecular mechanisms by which anticancer drugs affect LINC00973 expression and to define the consequences of its upregulation on drug resistance of cancer cells.

摘要

早期预测肿瘤复发取决于识别新的预后癌症生物标志物,这些标志物适用于监测肿瘤对不同化疗药物的反应。通过 RNA-Seq、RT-qPCR、生物信息学以及利用小鼠肿瘤异种移植模型的研究,我们发现了在不同剂量和时间用 5-氟尿嘧啶、奥沙利铂和伊立替康处理 HT-29 和 HCT-116 细胞时,五个 lincRNA(LINC00973、LINC00941、CASC19、CCAT1 和 BCAR4)的丰度存在显著且一致的变化;无论是在体外还是在体内。LINC00973 的变化最为频繁,在用三种化疗药物处理两种结肠癌细胞系时,其含量增加最为强烈和一致。需要进一步研究以确定抗癌药物影响 LINC00973 表达的分子机制,并确定其上调对癌细胞耐药性的后果。

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