LncRNA-MSC-AS1 inhibits the ovarian cancer progression by targeting miR-425-5p

Yinling Zhao1, Donglan Yuan2, Dandan Zhu1

  • 1Department of Obstetrics and Gynaecology, Taizhou People's Hospital, 399 Hailing South Road, Taizhou, 225300, Jiangsu, China.

Abstract

Insights

Long non-coding RNA MSC-AS1 inhibits ovarian cancer progression by sponging microRNA-425-5p. This interaction suppresses cell proliferation and promotes apoptosis, offering a potential therapeutic target for ovarian cancer treatment.

Area of Science:

  • Molecular Biology
  • Oncology
  • Genetics

Background:

  • Aberrant expression of long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) is linked to ovarian cancer pathogenesis.
  • The specific role and regulatory mechanisms of lncRNA MSC-AS1 in ovarian cancer remain unclear.

Purpose of the Study:

  • To investigate the role of lncRNA MSC-AS1 in ovarian cancer.
  • To elucidate the regulatory mechanism of MSC-AS1 involving microRNA-425-5p in ovarian cancer.

Main Methods:

  • Quantitative real-time PCR (qRT-PCR) to assess MSC-AS1 and miR-425-5p expression in ovarian cancer tissues and cell lines.
  • MTT, colony formation, and flow cytometry assays to evaluate MSC-AS1 function on cell proliferation, cell cycle, and apoptosis.
  • Western blot for protein expression analysis and dual-luciferase reporter assay to confirm the targeting relationship between MSC-AS1 and miR-425-5p.

Main Results:

  • MSC-AS1 was lowly expressed, while miR-425-5p was highly expressed in ovarian cancer tissues and cells.
  • Overexpression of MSC-AS1 inhibited ovarian cancer cell proliferation and induced apoptosis in SKOV3 and A2780 cells.
  • MSC-AS1 directly targeted and negatively regulated miR-425-5p; miR-425-5p upregulation partially reversed the tumor-suppressive effects of MSC-AS1.

Conclusions:

  • MSC-AS1 acts as a tumor suppressor in ovarian cancer by sponging miR-425-5p, thereby inhibiting cancer progression.
  • The MSC-AS1/miR-425-5p axis represents a potential therapeutic target for ovarian cancer treatment.

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 the pre-miRNA...
3.3K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
9.1K
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...
4.0K
Experimental RNAi02:15

Experimental RNAi

RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
6.5K