Gap junctions and connexins as therapeutic targets in cancer

Mustapha Kandouz1, Gerald Batist

  • 1Wayne State University, Department of Pathology, 5101 Cass Avenue, Chemistry Building, Detroit, Michigan 48202, USA. ag1764@wayne.edu

Abstract

Insights

Targeting connexins (Cxs) and gap junctional intercellular communications (GJICs) offers novel cancer therapies. Restoring Cxs expression and leveraging their functions show promise for eliminating cancer cells and enhancing treatment efficacy.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cell Biology

Background:

  • Connexins (Cxs) and gap junctional intercellular communications (GJICs) are implicated in cancer progression.
  • Targeting Cxs presents a novel strategy for cancer treatment, potentially inhibiting tumor growth or sensitizing cells to therapy.

Purpose of the Study:

  • To review therapeutic strategies involving connexins and gap junctions in cancer treatment.
  • To explore the role of Cxs in gene therapy, chemosensitization, apoptosis, and microenvironment interactions.

Main Methods:

  • Literature review focusing on therapeutic aspects of Cxs in cancer.
  • Analysis of strategies to restore connexin expression (transcriptional and post-transcriptional).

Main Results:

  • Connexins facilitate cancer cell elimination through bystander effects, chemosensitization, and modulation of apoptosis.
  • Strategies to restore connexin expression and leverage their functions are being explored.
  • The potential and limitations of these connexin-based therapeutic approaches are discussed.

Conclusions:

  • Connexins exhibit diverse roles in cancer, acting individually, in complexes, or interacting with other proteins.
  • Selective manipulation of Cxs expression remains challenging due to unresolved regulatory mechanisms.
  • Further research into connexin regulation and function is crucial to fully realize their therapeutic potential.

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