Micro-RNAs targeting the estrogen receptor alpha involved in endocrine therapy resistance in breast cancer

J M Márquez-Mendoza1, N Baranda-Ávila2, M Lizano3

  • 1Programa de Doctorado en Ciencias Biomédicas, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico City 04510, Mexico.

Insights

MicroRNAs (miRNAs) targeting estrogen receptor alpha (ERα) mRNA are key players in endocrine therapy resistance (ETR) in breast cancer (BC). Understanding these miRNA mechanisms is crucial for overcoming ETR in BC patients.

Area of Science:

  • Oncology
  • Genetics
  • Molecular Biology

Background:

  • Endocrine therapy resistance (ETR) is a significant challenge in breast cancer (BC) treatment.
  • Alterations in the tumor cell interactome, including non-coding RNAs (ncRNAs), contribute to ETR.
  • Micro-RNAs (miRNAs) are ncRNAs that regulate gene expression, impacting cancer development and treatment response.

Purpose of the Study:

  • To review the effects of miRNAs targeting estrogen receptor alpha (ERα) mRNA in breast cancer.
  • To elucidate the mechanisms by which these miRNAs contribute to endocrine therapy resistance (ETR).
  • To enhance the understanding of ETR in breast cancer through the study of miRNA involvement.

Main Methods:

  • Comprehensive literature review on miRNAs targeting ERα mRNA and ETR in BC.
  • In silico analysis to identify and validate miRNA-mRNA interactions.
  • Examination of the molecular mechanisms underlying miRNA-mediated ERα regulation.

Main Results:

  • Identified specific miRNAs that directly target ERα mRNA.
  • Elucidated diverse mechanisms through which these miRNAs influence ERα expression and ETR.
  • Demonstrated the significant role of miRNA-ERα interactions in the development of endocrine therapy resistance.

Conclusions:

  • miRNAs targeting ERα mRNA are critical modulators of endocrine therapy resistance in breast cancer.
  • Targeting these specific miRNAs presents a potential therapeutic strategy to overcome ETR.
  • Further research into miRNA-ERα interactions can lead to novel treatment approaches for breast cancer.

Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
21.1K
Internal Receptors01:31

Internal Receptors

Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
69.2K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.4K
Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
6.4K