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Published on: April 22, 2019
Apoptosis resistance-related ABCB5 and DNaseX (Apo10) expression in oral carcinogenesis
Martin Grimm1, Marcel Cetindis, Max Lehmann
1Department of Oral and Maxillofacial Surgery.
Background:
Apoptosis resistance is a crucial factor for the carcinogenesis of oral squamous cell carcinoma (OSCC).
Methods:
Expression of apoptosis resistance-related ATP-binding cassette (ABC) transporter ABCB5 [subfamily B (MDR/TAP) member 5] and DNaseX (Apo10) were analyzed in normal oral mucosa (n = 5), oral precursor lesions (simple hyperplasia, n = 11; squamous intraepithelial neoplasia, SIN I-III, n = 35), and OSCC specimen (n = 42) by immunohistochemistry.
Results:
Expression of ABCB5 and Apo10 were significantly increased in the carcinogenesis of OSCC compared with normal tissue. Compared with SIN I-III, ABCB5 expression was significantly decreased in OSCC. Apo10 expression did not significantly differ from OSCC compared with SIN I-III.
Conclusions:
This study provides the first evidence of the expression of ABCB5 and Apo10 in the multi-step carcinogenesis of OSCC. Overcoming drug resistance of ABCB5+ and Apo10+ cells in precursor lesions and tumors by natural compounds may act as sensitizers for apoptosis or could be useful for chemoprevention.
Insights
Apoptosis resistance in oral cancer involves ATP-binding cassette (ABC) transporter ABCB5 and DNaseX (Apo10). Their expression increases during oral squamous cell carcinoma (OSCC) development, suggesting potential targets for chemoprevention.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Apoptosis resistance is a key driver in oral squamous cell carcinoma (OSCC) development.
- Understanding molecular mechanisms of resistance is crucial for effective cancer treatment and prevention.
Purpose of the Study:
- To investigate the expression of ATP-binding cassette (ABC) transporter ABCB5 and DNaseX (Apo10) in oral carcinogenesis.
- To evaluate the role of these proteins in the progression from normal oral mucosa to OSCC.
Main Methods:
- Immunohistochemistry was used to analyze ABCB5 and Apo10 expression.
- Specimens included normal oral mucosa, oral precursor lesions (hyperplasia, SIN I-III), and OSCC.
Main Results:
- ABCB5 and Apo10 expression were significantly elevated in OSCC compared to normal tissues.
- ABCB5 expression decreased in OSCC relative to precursor lesions (SIN I-III).
- Apo10 expression showed no significant difference between OSCC and SIN I-III.
Conclusions:
- This study presents novel findings on ABCB5 and Apo10 expression during multi-step OSCC carcinogenesis.
- Targeting drug resistance in ABCB5+ and Apo10+ cells using natural compounds could enhance apoptosis sensitivity.
- These findings suggest potential applications in chemoprevention strategies for OSCC.
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