Abstract

Ion and water channels were recently shown to be involved in cancer cell functions, and various transporter types have been detected in upper gastrointestinal tract (UGI) cancers. Current information on the expression and roles of these channels and transporters in the death and survival of UGI cancer cells was reviewed herein, and the potential of their regulation for cancer management was investigated. Esophageal cancer (EC) and gastric cancer (GC) cells and tissues express many different types of ion channels, including voltage-gated K+, Cl–, and Ca2+, and transient receptor potential (TRP) channels, which regulate the progression of cancer. Aquaporin (AQP) 1, 3, and 5 are water channels that contribute to the progression of esophageal squamous cell carcinoma (ESCC) and GC. Intracellular pH regulators, including the anion exchanger (AE), sodium hydrogen exchanger (NHE), and vacuolar H+-ATPases (V-ATPase), also play roles in the functions of UGI cancer cells. We have previously conducted gene expression profiling and revealed that the regulatory mechanisms underlying apoptosis in ESCC cells involved various types of Cl– channels, Ca2+ channels, water channels, and pH regulators (Shimizu et al., 2014; Ariyoshi et al., 2017; Shiozaki et al., 2017, 2018a; Kobayashi et al., 2018; Yamazato et al., 2018; Konishi et al., 2019; Kudou et al., 2019; Katsurahara et al., 2020, 2021; Matsumoto et al., 2021; Mitsuda et al., 2021). We have also previously demonstrated the clinicopathological and prognostic significance of their expression in ESCC patients, and shown that their pharmacological blockage and gene silencing had an impact on carcinogenesis, indicating their potential as targets for the treatment of UGI cancers. A more detailed understanding of the molecular regulatory mechanisms underlying cell death and survival of UGI cancers may result in the application of cellular physiological methods as novel therapeutic approaches.

Highlights

  • Channels in the Cell Death and Survival of Upper GastrointestinalIon and water channels were recently shown to be involved in cancer cell functions, and various transporter types have been detected in upper gastrointestinal tract (UGI) cancers

  • Upper gastrointestinal tract (UGI) cancers, such as esophageal cancer (EC) and gastric cancer (GC), have high recurrence rates and are one of the leading causes of cancer-related death globally (Kamangar et al, 2006; Brenner et al, 2009; Hartgrink et al, 2009)

  • We previously reported the induction of apoptosis in esophageal squamous cell carcinoma (ESCC) via the Toll-like receptor 2 (TLR2)/c-Jun N-terminal kinase (JNK) pathway by the genetic knockdown of chloride intracellular channel 1 (CLIC1) with small interfering RNA (siRNA) technology (Kobayashi et al, 2018)

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Summary

Channels in the Cell Death and Survival of Upper Gastrointestinal

Ion and water channels were recently shown to be involved in cancer cell functions, and various transporter types have been detected in upper gastrointestinal tract (UGI) cancers. We have previously conducted gene expression profiling and revealed that the regulatory mechanisms underlying apoptosis in ESCC cells involved various types of Cl− channels, Ca2+ channels, water channels, and pH regulators (Shimizu et al, 2014; Ariyoshi et al, 2017; Shiozaki et al, 2017, 2018a; Kobayashi et al, 2018; Yamazato et al, 2018; Konishi et al, 2019; Kudou et al, 2019; Katsurahara et al, 2020, 2021; Matsumoto et al, 2021; Mitsuda et al, 2021).

INTRODUCTION
Centrosomerelated genes
Overexpression vector
Water Channels
Death receptor signaling pathway
GC GC
Findings
CONCLUSION
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