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Updated: Jun 28, 2025

Profiling of Estrogen-regulated MicroRNAs in Breast Cancer Cells
Published on: February 21, 2014
The regulation of microRNAs on chemoresistance in triple-negative breast cancer: a recent update
Li-Jun Yan1, Andy T Y Lau1, Yan-Ming Xu1
1Laboratory of Cancer Biology & Epigenetics, Department of Cell Biology & Genetics, Shantou University Medical College, Shantou, 515041, China.
Abstract:
Triple-negative breast cancer (TNBC) has negative expressions of ER, PR and HER2. Due to the insensitivity to both endocrine therapy and HER2-targeted therapy, the main treatment method for TNBC is cytotoxic chemotherapy. However, the curative effect of chemotherapy is limited because of the existence of acquired or intrinsic multidrug resistance. MicroRNAs (miRNAs) are frequently dysregulated in malignant tumors and involved in tumor occurrence and progression. Interestingly, growing studies show that miRNAs are involved in chemoresistance in TNBC. Thus, targeting dysregulated miRNAs could be a plausible way for better treatment of TNBC. Here, we present the updated knowledge of miRNAs associated with chemoresistance in TNBC, which may be helpful for the early diagnosis, prognosis and treatment of this life-threatening disease.
Insights
Triple-negative breast cancer (TNBC) often resists chemotherapy due to multidrug resistance. Targeting microRNAs (miRNAs) shows promise for improving TNBC treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) lacks ER, PR, and HER2 expression, necessitating chemotherapy.
- Chemotherapy efficacy in TNBC is limited by intrinsic and acquired multidrug resistance.
- MicroRNAs (miRNAs) are small non-coding RNAs frequently dysregulated in cancers and implicated in tumor progression.
Purpose of the Study:
- To review and synthesize current knowledge on the role of microRNAs in chemoresistance within TNBC.
- To highlight the potential of targeting dysregulated miRNAs for enhancing TNBC treatment strategies.
Main Methods:
- Literature review of studies investigating microRNAs and chemoresistance in TNBC.
- Analysis of reported associations between specific miRNA dysregulation and chemotherapy response in TNBC models and patients.
Main Results:
- MicroRNAs are demonstrably involved in the development of chemoresistance in TNBC.
- Dysregulation of various miRNAs contributes to both intrinsic and acquired multidrug resistance in TNBC.
- Specific miRNAs have been identified as potential biomarkers for predicting chemoresistance.
Conclusions:
- Targeting dysregulated miRNAs presents a promising therapeutic avenue for overcoming chemoresistance in TNBC.
- Understanding miRNA involvement in chemoresistance can aid in developing novel diagnostic and prognostic tools for TNBC.
- Further research into miRNA-based therapies could significantly improve treatment outcomes for TNBC patients.
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