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Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
miRNA clusters as therapeutic targets for hormone-resistant breast cancer
Gianpiero Di Leva1, Douglas G Cheung1, Carlo M Croce1
1Department of Molecular Virology Immunology and Medical Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, OH, 43210, USA.
Abstract:
MicroRNAs are small non coding RNAs that typically inhibit the translation and stability of messenger RNAs, controlling genes involved in cellular processes such as inflammation, cell cycle regulation, stress response, differentiation, apoptosis, and migration. Not surprisingly, microRNAs are also aberrantly expressed in cancer and promote tumorigenesis by disrupting these vital cellular functions. In this review, we first broadly summarize the role of microRNAs in breast cancer and Estrogen Receptor alpha signaling. Then we focus on what is currently known about the role of microRNAs in anti-hormonal therapy or resistance to endocrine agents. Specifically, we will discuss key miRNAs involved in tamoxifen (miR-221/222, 181, 101, 519a, 301, 375, 342, 451, and the let-7 family), fulvestrant (miR-221/222, miR-200 family), and aromatase inhibitor (miR-128 and the let-7 family) resistance.
Insights
MicroRNAs (miRNAs) are key regulators in breast cancer. This review explores how specific miRNAs influence response and resistance to endocrine therapies like tamoxifen and aromatase inhibitors.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs regulating gene expression.
- Aberrant miRNA expression is implicated in cancer development and progression.
- Estrogen Receptor alpha (ERα) signaling is crucial in breast cancer.
Purpose of the Study:
- To review the role of miRNAs in breast cancer.
- To examine miRNA involvement in endocrine therapy response and resistance.
- To highlight specific miRNAs associated with resistance to tamoxifen, fulvestrant, and aromatase inhibitors.
Main Methods:
- Literature review of scientific articles.
- Analysis of miRNA roles in cellular processes and cancer.
- Focus on miRNA involvement in endocrine therapy resistance mechanisms.
Main Results:
- miRNAs regulate vital cellular functions disrupted in cancer.
- Specific miRNAs are linked to tamoxifen resistance (e.g., miR-221/222, let-7 family).
- Other miRNAs are associated with fulvestrant (e.g., miR-200 family) and aromatase inhibitor resistance (e.g., miR-128, let-7 family).
Conclusions:
- miRNAs play a significant role in breast cancer pathogenesis.
- miRNAs are critical mediators of resistance to endocrine therapies.
- Targeting specific miRNAs may offer novel therapeutic strategies for overcoming endocrine resistance.
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