Abstract

Despite concerted clinical and research efforts, cancer is a leading cause of death worldwide. Surgery, radiation, and chemotherapy have remained the most common standard-of-care strategies against cancer for decades. However, the side effects of these therapies demonstrate the need to investigate adjuvant novel treatment modalities that minimize the harm caused to healthy cells and tissues. Normal and cancerous cells require communication amongst themselves and with their surroundings to proliferate and drive tumor growth. It is vital to understand how intercellular and external communication impacts tumor cell malignancy. To survive and grow, tumor cells, and their normal counterparts utilize cell junction molecules including gap junctions (GJs), tight junctions, and adherens junctions to provide contact points between neighboring cells and the extracellular matrix. GJs are specialized structures composed of a family of connexin proteins that allow the free diffusion of small molecules and ions directly from the cytoplasm of adjacent cells, without encountering the extracellular milieu, which enables rapid, and coordinated cellular responses to internal and external stimuli. Importantly, connexins perform three main cellular functions. They enable direct gap junction intercellular communication (GJIC) between cells, form hemichannels to allow cell communication with the extracellular environment, and serve as a site for protein-protein interactions to regulate signaling pathways. Connexins themselves have been found to promote tumor cell growth and invasiveness, contributing to the overall tumorigenicity and have emerged as attractive anti-tumor targets due to their functional diversity. However, connexins can also serve as tumor suppressors, and therefore, a complete understanding of the roles of the connexins and GJs in physiological and pathophysiological conditions is needed before connexin targeting strategies are applied. Here, we discuss how the three aspects of connexin function, namely GJIC, hemichannel formation, and connexin-protein interactions, function in normal cells, and contribute to tumor cell growth, proliferation, and death. Finally, we discuss the current state of anti-connexin therapies and speculate which role may be most amenable for the development of targeting strategies.

Highlights

  • To ensure the proper coordination of tissue function, rapid intercellular communication is required between individual cells, as well as between cells and their microenvironment [1]

  • Over the past 50 years, remarkable work has been conducted to investigate how connexins function in cell-cell communication, hemichannel activity, and other activities unrelated to gap junction intercellular communication (GJIC)

  • Proper cellular adhesion and communication are necessary for the development of multicellular life, without which it would not be possible to coordinate larger-scale behavior and cellular responses

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Summary

Introduction

To ensure the proper coordination of tissue function, rapid intercellular communication is required between individual cells, as well as between cells and their microenvironment [1]. Disruption of adhesion complexes has typically been understood to interfere with normal tissue function and serves as the initiating event for pathophysiological disorders. Among such mechanisms, intercellular communication mediated by GJs has been found to be vital for the maintenance of cell survival in a variety of different tissues [7]. Each connexin has tissue- and developmental specific functions in mammalian biology, redundancy does exist between subunits [6] This has been experimentally demonstrated, as different connexin isoforms display spatial and temporal specificity, which is modulated by transcription factors including the Sp transcription factors (Sp1 and Sp3), activator protein (AP-1), and members of the Jak/STAT pathway [9]. Cell-specific transcription factors such as Nkx, HNF-1, Mist, and NF-κB, among others, can regulate connexin gene expression, allowing for precise expression of connexins during development and homeostasis [10]

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