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

被引:33
作者
Zinovieva, Olga L. [1 ]
Grineva, Evgenia N. [1 ]
Prokofjeva, Maria M. [1 ]
Karpov, Dmitry S. [1 ,2 ]
Zheltukhin, Andrei O. [1 ]
Krasnov, George S. [1 ,2 ]
Snezhkina, Anastasiya V. [1 ]
Kudryavtseva, Anna V. [1 ]
Chumakov, Peter M. [1 ]
Mashkova, Tamara D. [1 ]
Prassolov, Vladimir S. [1 ]
Lisitsyn, Nikolai A. [1 ]
机构
[1] Russian Acad Sci, Engelhardt Inst Mol Biol, Vavilova Str 32, Moscow 119991, Russia
[2] Russian Acad Sci, Inst Biomed Chem, Moscow 119121, Russia
基金
俄罗斯科学基金会;
关键词
lncRNA; Colorectal cancer; RNA-Seq; Chemotherapeutic drugs; Cancer biomarkers; GENE-EXPRESSION; CISPLATIN RESISTANCE; BREAST-CANCER; P53; 5-FLUOROURACIL;
D O I
10.1016/j.biochi.2018.05.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2018 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
引用
收藏
页码:67 / 72
页数:6
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