MiR-718 represses VEGF and inhibits ovarian cancer cell progression

Ruobing Leng1, Lang Zha2, Liangdan Tang1

  • 1Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, People's Republic of China.

FEBS Letters
|May 13, 2014
PubMed

Insights

Restoring microRNA-718 (miR-718) expression inhibits ovarian cancer growth by targeting vascular endothelial growth factor (VEGF). This finding offers a potential new therapeutic strategy for ovarian cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Vascular endothelial growth factor (VEGF) oncogenic activation is implicated in various cancers, including ovarian cancer.
  • MicroRNAs (miRNAs) are key regulators of gene expression and play critical roles in cancer development.

Purpose of the Study:

  • To investigate the role of miR-718 in regulating VEGF expression in ovarian cancer.
  • To explore the therapeutic potential of restoring miR-718 in ovarian cancer.

Main Methods:

  • Correlation analysis of miR-718 and VEGF expression in ovarian cancer tissues.
  • Luciferase reporter assays to confirm direct targeting of VEGF by miR-718.
  • In vitro and in vivo assays to assess the effect of miR-718 restoration on ovarian cancer proliferation.
  • Western blot analysis to evaluate the impact of VEGF on AKT phosphorylation.

Main Results:

  • miR-718 expression is significantly downregulated in ovarian cancer specimens and inversely correlates with VEGF levels.
  • miR-718 directly targets and represses VEGF expression.
  • Restoration of miR-718 inhibits ovarian cancer cell proliferation in vitro and tumor growth in vivo.
  • VEGF overexpression can counteract the anti-proliferative effects of miR-718 by increasing phosphorylated AKT levels.

Conclusions:

  • miR-718 acts as a tumor suppressor in ovarian cancer by inhibiting VEGF expression.
  • Restoring miR-718 represents a promising therapeutic strategy for ovarian cancer, targeting the VEGF pathway.

Related Concept Videos

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...
3.6K
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
6.2K
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...
3.0K
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...
6.3K
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,...
3.7K
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
2.9K