Decreased miR-124-3p Expression Prompted Breast Cancer Cell Progression Mainly by Targeting Beclin-1

Clinical Laboratory
|July 30, 2016
PubMed
Abstract

Insights

MicroRNA-124-3p (miR-124-3p) is decreased in breast cancer, promoting cell progression by increasing Beclin-1 and autophagy. Restoring miR-124-3p levels may offer therapeutic potential.

Area of Science:

  • Oncology
  • Molecular Biology
  • Gene Regulation

Background:

  • Aberrant microRNA (miRNA) expression is linked to cancer development.
  • This study identifies a novel miRNA regulating Beclin-1 in breast cancer.

Purpose of the Study:

  • To investigate the role of miR-124-3p in breast cancer.
  • To determine if Beclin-1 is a target gene of miR-124-3p.

Main Methods:

  • Expression analysis of miR-124-3p and Beclin-1 in breast cancer tissues and cell lines.
  • Luciferase reporter assay to confirm Beclin-1 as a miR-124-3p target.
  • Western blot and qRT-PCR to assess autophagy-related protein expression.

Main Results:

  • miR-124-3p expression is significantly decreased in breast cancer.
  • miR-124-3p negatively regulates Beclin-1 expression.
  • Overexpression of miR-124-3p reduces Beclin-1 and LC3II levels, partially reversing 4-OHT-induced autophagy.

Conclusions:

  • Downregulation of miR-124-3p promotes breast cancer progression.
  • This progression is mediated by enhanced expression of the autophagy protein Beclin-1.
  • miR-124-3p acts as a tumor suppressor in breast cancer by inhibiting autophagy.

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...
24.5K
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 the pre-miRNA...
4.2K
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
5.4K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
5.0K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
6.1K