Literature DB >> 27959276

Identification and targeting of microRNAs modulating acquired chemotherapy resistance in Triple negative breast cancer (TNBC): A better strategy to combat chemoresistance.

Samayita Das1.   

Abstract

Triple negative breast cancer (TNBC) is a heterogeneous form of malignant disease. Due to lack of proper therapeutic target treatment options are restricted and relies primarily on chemotherapeutic modality for treatment of patients. Despite significant early regression of the disease in response to chemotherapy, complete cure is not assured with development of resistant tumors which is difficult to manage clinically. In the last decades, the regulation and contribution of microRNAs in tumorigenesis including breast cancers have been well-documented. Thus, here it is hypothesized that by identifying the microRNAs responsible for chemoresistance in TNBC and targeting the microRNAs along with chemotherapeutic approaches might exert an improved response. To accomplish this, an in vivo screening has to be performed by transfecting tumor cell line with lentiviral pool of library expressing microRNAs. Following treatment of primary tumors in mice and growth of relapsed tumors, microRNA profile has to be analyzed by qRT-PCR and sequencing to detect the microRNAs contributing to the chemoresistance which can be targeted by anti-microRNA strategies.
Copyright © 2016 Elsevier Ltd. All rights reserved.

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Year:  2016        PMID: 27959276     DOI: 10.1016/j.mehy.2016.09.004

Source DB:  PubMed          Journal:  Med Hypotheses        ISSN: 0306-9877            Impact factor:   1.538


  3 in total

1.  MicroRNA-216a suppresses the proliferation and migration of human breast cancer cells via the Wnt/β-catenin signaling pathway.

Authors:  Qing Xie; Shuai Wang; Yue Zhao; Zhenchao Zhang; Chuan Qin; Xianjun Yang
Journal:  Oncol Rep       Date:  2019-03-07       Impact factor: 3.906

2.  MicroRNA-598 inhibits the growth of triple negative breast cancer cells by targeting JAG1.

Authors:  Guohui Han; Xiangdong Bai; Hongchuan Jiang; Qiang He
Journal:  Exp Ther Med       Date:  2021-01-21       Impact factor: 2.447

3.  Study on the Mechanism of Cell Cycle Checkpoint Kinase 2 (CHEK2) Gene Dysfunction in Chemotherapeutic Drug Resistance of Triple Negative Breast Cancer Cells.

Authors:  Li Luo; Wei Gao; Jinghui Wang; Dingxue Wang; Xiaobo Peng; Zhaoyang Jia; Ye Jiang; Gongzhuo Li; Dongxin Tang; Yajie Wang
Journal:  Med Sci Monit       Date:  2018-05-15
  3 in total

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