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Updated: Jun 29, 2025

Profiling of Estrogen-regulated MicroRNAs in Breast Cancer Cells
Published on: February 21, 2014
Therapeutic significance of long noncoding RNAs in estrogen receptor-positive breast cancer
Abdullah Ali Alzahrani1, Raed Obaid Saleh2, Amaliya Latypova3,4
1Department of Surgery, Taif University, Taif, Saudi Arabia.
Abstract:
About 70% of cases of breast cancer are compromised by Estrogen-positive breast cancer. Through its regulation of several processes, including cell proliferation, cell cycle progression, and apoptosis, Estrogen signaling plays a pivotal role in the genesis and progression of this particular kind of breast cancer. One of the best treatment strategies for treating Estrogen-positive breast cancer is blocking Estrogen signaling. However, patients' treatment failure is mainly caused by the emergence of resistance and metastases, necessitating the development of novel therapeutic targets. Numerous studies have shown long noncoding RNAs (lncRNAs) to play a role in Estrogen-mediated carcinogenesis. These lncRNAs interact with co-regulators and the Estrogen signaling cascade components, primarily due to Estrogen activation. Vimentin and E-cadherin are examples of epithelial-to-mesenchymal transition markers, and they regulate genes involved in cell cycle progression, such as Cyclins, to affect the growth, proliferation, and metastasis of Estrogen-positive breast cancer. Furthermore, a few of these lncRNAs contribute to developing resistance to chemotherapy, making them more desirable targets for enhancing results. Thus, to shed light on the creation of fresh approaches for treating this cancer, this review attempts to compile recently conducted studies on the relationship between lncRNAs and the advancement of Estrogen-positive breast cancer.
Insights
Estrogen-positive breast cancer is driven by Estrogen signaling. Long noncoding RNAs (lncRNAs) are implicated in Estrogen-mediated carcinogenesis and may offer new therapeutic targets for overcoming treatment resistance.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Estrogen signaling is crucial in ~70% of breast cancers, driving proliferation, cell cycle, and apoptosis.
- Blocking Estrogen signaling is a key treatment, but resistance and metastasis limit efficacy.
- Novel therapeutic targets are needed to improve outcomes for Estrogen-positive breast cancer.
Purpose of the Study:
- To review recent studies on the role of long noncoding RNAs (lncRNAs) in Estrogen-positive breast cancer.
- To highlight lncRNAs as potential targets for overcoming treatment resistance and metastasis.
- To inform the development of novel therapeutic strategies.
Main Methods:
- Literature review of recent studies on lncRNAs and Estrogen-positive breast cancer.
- Analysis of lncRNA interactions with Estrogen signaling pathways and co-regulators.
- Examination of lncRNA involvement in epithelial-to-mesenchymal transition (EMT) markers and cell cycle regulation.
Main Results:
- lncRNAs are implicated in Estrogen-mediated carcinogenesis and interact with Estrogen signaling components.
- Specific lncRNAs regulate EMT markers (e.g., Vimentin, E-cadherin) and cell cycle genes (e.g., Cyclins).
- Some lncRNAs contribute to chemotherapy resistance, suggesting their potential as therapeutic targets.
Conclusions:
- lncRNAs play a significant role in the growth, proliferation, and metastasis of Estrogen-positive breast cancer.
- Targeting lncRNAs may offer a promising strategy to overcome treatment resistance and improve patient outcomes.
- Further research into lncRNA functions can lead to new therapeutic approaches for this disease.
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