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Updated: Jul 19, 2026

Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics
Published on: May 11, 2016
Connexin expression and gap junctional intercellular communication in human squamous cell carcinoma of the head and
Douglas K Frank1, Bozena Szymkowiak, Cynthia A Hughes
1Department of Otolaryngology-Head and Neck Surgery and the Head and Neck Cancer Molecular Biology Research Laboratory, Division of Basic Sciences, New York, New York, USA. dfrank@bethisraelny.org
Objective:
Our laboratory is investigating the role that gap junction intercellular channels (composed of proteins called connexins) play in communicating apoptotic signals from therapeutically targeted squamous cell carcinoma of the head and neck (SCCHN) cells to adjacent, untreated, "bystander" cells (bystander effect). The nature of this research underscores the importance of delineating connexin expression patterns in SCCHN, and how this correlates with gap junctional intercellular communication (GJIC) and bystander effects.
Study Design:
The GJIC activity of a diverse panel of SCCHN cell lines, as well as normal oral epithelial (NOE) cell controls was determined in vitro. These data were correlated with connexin expression patterns determined through connexin 43 and connexin 26 immunofluorescence.
Results:
Cell lines with retained GJIC activity all expressed connexin 43 on the cell membrane. Cell lines that did not communicate microinjected lucifer yellow (lost GJIC activity) showed no connexin expression, either at the cell membrane or in the cytosol. Connexin 26 was not expressed in any of our SCCHN cell lines, whereas both connexin 43 and connexin 26 were expressed in the NOE cell controls. Furthermore, connexin 43 introduction into a GJIC (and connexin) deficient SCCHN cell line conferred no growth inhibitory effect.
Conclusion:
Connexin 43 expression correlates with retained GJIC in SCCHN in vitro. Connexin 26 may have a role as a tumor suppressor in SCCHN.
Significance:
The data presented have relevance to our ongoing investigations of gap-junction mediated bystander effects in SCCHN and are being expanded to investigations on actual SCCHN tumor specimens.
Insights
Connexin 43 expression correlates with gap junction communication in head and neck squamous cell carcinoma. Connexin 26 may act as a tumor suppressor in these cancers.
Area of Science:
- Oncology
- Cell Biology
- Molecular Biology
Background:
- Gap junction intercellular channels (GJIC) mediate communication between cells.
- Connexins are proteins that form gap junctions.
- Understanding connexin roles in cancer is crucial for therapeutic development.
Purpose of the Study:
- Investigate connexin expression in squamous cell carcinoma of the head and neck (SCCHN).
- Correlate connexin patterns with GJIC and bystander effects in SCCHN.
- Determine the role of connexin 43 and 26 in SCCHN.
Main Methods:
- Assessed GJIC activity in SCCHN cell lines and normal oral epithelial (NOE) cells in vitro.
- Determined connexin 43 and 26 expression using immunofluorescence.
- Correlated GJIC activity with connexin expression levels.
Main Results:
- SCCHN cell lines with retained GJIC expressed connexin 43.
- Loss of GJIC correlated with absent connexin expression.
- Connexin 26 was not found in SCCHN cell lines but was present in NOE cells.
- Introducing connexin 43 did not inhibit growth in deficient SCCHN cells.
Conclusions:
- Connexin 43 expression is linked to GJIC in SCCHN.
- Connexin 26 may function as a tumor suppressor in SCCHN.
- Findings support ongoing research into gap-junction mediated bystander effects in SCCHN.
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