MicroRNA-221-3p Plays an Oncogenic Role in Gastric Carcinoma by Inhibiting PTEN Expression

Jianping Shi1, Yi Zhang2, Nuyun Jin1

  • 1Department of Digestion, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, P.R. China.

Oncology Research
|October 8, 2016
PubMed

Insights

MicroRNA miR-221-3p promotes gastric carcinoma growth and spread. This microRNA targets PTEN, offering a potential therapeutic target for this common male malignancy.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Gastric carcinoma is a prevalent malignancy, particularly in men.
  • MicroRNAs are key regulators in cancer development and metastasis.
  • The specific role of miR-221-3p in gastric carcinoma remains largely unexplored.

Purpose of the Study:

  • To investigate the functional role of miR-221-3p in gastric carcinoma.
  • To determine the correlation between miR-221-3p expression and patient prognosis.
  • To elucidate the molecular mechanism underlying miR-221-3p's function in gastric cancer.

Main Methods:

  • Quantification of miR-221-3p expression in gastric cancer cell lines and patient tumor samples.
  • In vitro functional assays (proliferation, invasion, sphere formation) with miR-221-3p overexpression and silencing.
  • In vivo studies using xenograft mouse models.
  • Identification of miR-221-3p targets using molecular techniques.

Main Results:

  • miR-221-3p expression is significantly elevated in gastric carcinoma.
  • High miR-221-3p levels correlate with poor patient prognosis.
  • Overexpression of miR-221-3p enhances cancer cell proliferation, invasion, and sphere formation.
  • Silencing miR-221-3p inhibits these oncogenic properties.
  • miR-221-3p promotes tumor growth in vivo.
  • miR-221-3p directly targets PTEN mRNA, downregulating its expression.

Conclusions:

  • miR-221-3p acts as an oncogene in gastric carcinoma.
  • The miR-221-3p/PTEN axis is a critical pathway in gastric cancer progression.
  • miR-221-3p represents a potential therapeutic target for gastric carcinoma.

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
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.9K
Loss of Tumor Suppressor Gene Functions01:12

Loss of Tumor Suppressor Gene Functions

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
6.2K