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Updated: Jun 1, 2026

Modeling Oral-Esophageal Squamous Cell Carcinoma in 3D Organoids
Published on: December 23, 2022
The role of Ca2+ channels in oral squamous cell carcinoma development
Kana Hasegawa1, Shinsuke Fujii2, Tamotsu Kiyoshima1
1Laboratory of Oral Pathology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Background:
Oral squamous cell carcinoma (OSCC) arises from the mucosal epithelium and is the most common cancer of the oral cavity. There are few major oncogenic events that could be therapeutically targeted in OSCC; therefore, the identification of novel target factors based on the molecular mechanisms of the tumorigenesis of OSCC is required.
Highlight:
The extracellular matrix (ECM), a component of the tumor microenvironment, surrounds tumor cells, and it provides a scaffold for tumors. The ECM promotes tumor progression, and mechanical cues from increased ECM stiffness are involved in tumorigenesis. Recently, mechanosensitive ion channels have been identified as receptors for the ECM. Mechanosensitive ion channels respond to mechanical cues, alter intracellular signaling and affect tumor cell behavior such as cell proliferation. This review explores the role of the ECM and its receptors, mechanosensitive ion channels, and particularly Ca2+ channels.
Conclusion:
Mechanosensitive Ca2+ channels, Piezo-type mechanosensitive ion channel component 1 and transient receptor potential vanilloid 4, promote tumorigenesis of OSCC. We demonstrated that Ca2+ channels may represent novel molecular targets in OSCC.
Insights
Mechanosensitive calcium channels, like Piezo1 and TRPV4, are crucial in oral squamous cell carcinoma (OSCC) development. Targeting these channels offers a promising new therapeutic strategy for OSCC.
Area of Science:
- Oncology
- Cell Biology
- Biophysics
Background:
- Oral squamous cell carcinoma (OSCC) is the most prevalent oral malignancy.
- Limited therapeutic targets exist for OSCC, necessitating research into novel molecular mechanisms.
- Understanding OSCC tumorigenesis requires identifying key factors driving cancer development.
Purpose of the Study:
- To review the role of the extracellular matrix (ECM) and its mechanosensitive ion channel receptors in OSCC.
- To explore the involvement of mechanosensitive calcium (Ca2+) channels in OSCC progression.
- To identify potential novel molecular targets for OSCC therapy.
Main Methods:
- Literature review focusing on the extracellular matrix (ECM) and mechanosensitive ion channels.
- Analysis of studies investigating the function of ECM stiffness and mechanosensitive channels in cancer.
- Examination of specific Ca2+ channels, including Piezo1 and TRPV4, in the context of OSCC.
Main Results:
- The ECM, a component of the tumor microenvironment, supports tumor growth and progression.
- Increased ECM stiffness provides mechanical cues that contribute to tumorigenesis.
- Mechanosensitive ion channels act as ECM receptors, translating mechanical signals into cellular responses.
- These channels influence intracellular signaling pathways, affecting tumor cell proliferation and behavior.
Conclusions:
- Mechanosensitive Ca2+ channels, specifically Piezo1 and TRPV4, actively promote OSCC tumorigenesis.
- These Ca2+ channels represent potential novel molecular targets for therapeutic intervention in OSCC.
- Targeting mechanosensitive ion channels could offer a new strategy for treating oral cancer.
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