MicroRNAs in the anticancer effects of celecoxib: A systematic review

Mohammad Amir Mishan1, Mohammad Amin Khazeei Tabari2, Mehryar Zargari3

  • 1Ocular Tissue Engineering Research Center, Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Insights

Cyclooxygenase-2 (COX-2) drives cancer progression and metastasis. This review explores how the COX-2 inhibitor celecoxib, via microRNA (miRNA) regulation, offers therapeutic anticancer potential.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Cyclooxygenase-2 (COX-2) is a key enzyme in inflammation with a significant role in cancer development.
  • COX-2 promotes tumorigenesis via epithelial-to-mesenchymal transition (EMT), proliferation, migration, invasion, and metastasis.
  • MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression and are implicated in cancer as tumor suppressors or oncogenes.

Purpose of the Study:

  • To systematically review the tumorigenic role of COX-2 in various cancers.
  • To highlight the anticancer therapeutic effects of celecoxib, a selective COX-2 inhibitor.
  • To elucidate the involvement of miRNA regulation in COX-2-mediated cancer development and celecoxib's action.

Main Methods:

  • Systematic literature review.
  • Analysis of studies investigating COX-2, celecoxib, and miRNA interactions in cancer.
  • Synthesis of evidence on COX-2's tumorigenic mechanisms and celecoxib's therapeutic potential through miRNA modulation.

Main Results:

  • COX-2 significantly contributes to cancer progression and metastasis through various cellular mechanisms.
  • Celecoxib demonstrates anticancer potential by selectively inhibiting COX-2 and modulating downstream pathways.
  • Evidence indicates that COX-2 exerts its functions, in part, through the regulation of specific miRNAs.

Conclusions:

  • COX-2 plays a critical role in tumorigenesis and metastasis.
  • Celecoxib represents a promising therapeutic agent for cancer treatment by targeting COX-2 and influencing miRNA expression.
  • Targeting the COX-2-miRNA axis offers a novel strategy for cancer therapy.

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