MicroRNA signatures in chemotherapy resistant esophageal cancer cell lines

被引:66
|
作者
Hummel, Richard [1 ,2 ]
Sie, Corina [1 ]
Watson, David I. [1 ]
Wang, Tingting [1 ]
Ansar, Alfiya [1 ]
Michael, Michael Z. [3 ]
Van der Hoek, Mark [4 ]
Haier, Joerg [5 ]
Hussey, Damian J. [1 ]
机构
[1] Flinders Univ S Australia, Med Ctr, Dept Surg, Bedford Pk, SA 5042, Australia
[2] Univ Munster, Dept Gen & Visceral Surg, D-48149 Munster, Germany
[3] Flinders Univ S Australia, Dept Gastroenterol & Hepatol, Bedford Pk, SA 5042, Australia
[4] Adelaide Microarray Ctr, SA Pathol, Adelaide, SA 5000, Australia
[5] Univ Munster, Ctr Comprehens Canc, D-48149 Munster, Germany
基金
英国医学研究理事会;
关键词
Esophageal cancer; MicroRNA; Chemotherapy; Resistance; Target; MULTIDRUG-RESISTANCE; CONFERS RESISTANCE; CARCINOMA; CHEMORADIOTHERAPY; METAANALYSIS; SURVIVAL; RECEPTOR;
D O I
10.3748/wjg.v20.i40.14904
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate expression of microRNA (miRNA) and potential targets in chemotherapy resistant esophageal cancer cell lines. METHODS: An in-vitro model of acquired chemotherapy resistance in esophageal adeno- (EAC) and squamous cell carcinoma (ESCC) cells was used, and microRNA expression profiles for cisplatin or 5-fluorouracil (5-FU) resistant variants vs chemotherapy sensitive controls were compared using microarray and quantitative real-time polymerase chain reaction (PCR). The expression of chemotherapy-relevant genes potentially targeted by the dysregulated microRNAs in the chemotherapy resistant variants was also evaluated. RESULTS: Chemotherapy resistant sublines were found to have specific miRNA signatures, and these miRNA signatures were different for the cisplatin vs 5-FU resistant cells from the same tumor cell line, and also for EAC vs ESCC cells with resistance to the same specific chemotherapy agent. Amongst others, miR-27b-3p, miR-193b-3p, miR-192-5p, miR-378 a-3p, miR-125a-5p and miR-18a-3p were dysregulated, consistent with negative posttranscriptional control of KRAS, TYMS, ABCC3, CBL-B and ERBB2 expression via these miRNAs. CONCLUSION: The current study supports the hypothesis that microRNA expression has an impact on chemotherapy resistance in esophageal cancer. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:14904 / 14912
页数:9
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