Chemoresistance Mediated by ceRNA Networks Associated With the PVT1 Locus

Olorunseun O Ogunwobi1,2, Adithya Kumar1

  • 1Department of Biological Sciences, Hunter College of the City University of New York, New York, NY, United States.

Frontiers in Oncology
|September 12, 2019
PubMed

Insights

Competitive endogenous RNA (ceRNA) networks, particularly those involving long non-coding RNA PVT1 (lncPVT1), are key in cancer development. This review explores how lncPVT1-associated ceRNA networks contribute to chemoresistance in various human cancers.

Area of Science:

  • Molecular Biology
  • Genetics
  • Oncology

Background:

  • Competitive endogenous RNA (ceRNA) networks regulate gene expression through non-coding RNAs (ncRNAs).
  • ncRNAs from the 8q24 locus, notably lncPVT1, are implicated in human cancer development and progression.
  • Chemoresistance in cancer is linked to disrupted cellular processes like proliferation and epithelial-mesenchymal transition.

Purpose of the Study:

  • To review the literature on the role of ncRNAs from the PVT1 locus and their ceRNA networks.
  • To examine the contribution of these networks to the development of chemoresistance in human cancers.

Main Methods:

  • Literature review of recent studies.
  • Analysis of ncRNA-mediated regulatory mechanisms in ceRNA networks.
  • Focus on the PVT1 locus and its associated ncRNAs.

Main Results:

  • ceRNA networks, especially those involving lncPVT1, are critical regulators of carcinogenesis.
  • These networks modulate gene expression and protein activity via ncRNA sponging and epigenetic mechanisms.
  • Dysregulation of ceRNA networks contributes to chemoresistance by affecting cell proliferation, differentiation, and epithelial-mesenchymal transition.

Conclusions:

  • ncRNAs encoded by the PVT1 locus and their ceRNA networks play a significant role in cancer chemoresistance.
  • Understanding these networks offers potential therapeutic targets for overcoming treatment resistance.

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