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Published on: August 11, 2023
Diabetes and oral oncogenesis
Eleftherios Vairaktaris1, Sofia Spyridonidou, Lambros Goutzanis
1Department of Oral and Maxillofacial Surgery, University of Athens Medical School, Kifissias and Perikleous Stavrou 9, Athens 11524, Greece. lvairakt@med.uoa.gr
Diabetes promotes oral cancer development by activating specific cell signaling pathways, leading to increased cell proliferation without affecting apoptosis. This research highlights diabetes as a significant risk factor for oral squamous cell carcinoma (OSCC).
Area of Science:
- Oncology
- Endocrinology
- Molecular Biology
Background:
- Oral squamous cell carcinoma (OSCC) is a major global health concern.
- Epidemiological studies suggest a link between diabetes mellitus and increased OSCC risk.
- Understanding the molecular mechanisms underlying this association is crucial.
Purpose of the Study:
- To investigate the impact of diabetes on signal transduction pathways during oral cancer development.
- To analyze the expression of key oncogenes, tumor suppressor genes, and cell proliferation/apoptosis markers in an animal model of oral oncogenesis with diabetes.
Main Methods:
- An animal model was established using streptozotocin-induced diabetes and 4-nitroquinoline N-oxide for chemical carcinogenesis.
- Expression levels of various signaling molecules (e.g., EGFR, Ras/Raf/MAPK pathway components, p53, p16) and markers (Ki-67, Bax, Bcl-2) were analyzed.
- Sequential stages of oral cancer development were examined.
Main Results:
- Diabetes promoted the activation of the Ras/Raf/MAPK signal transduction pathway.
- This activation was primarily mediated by the induction of erbB2 and erbB3 receptors.
- Increased cell proliferation was observed in diabetic rats, while apoptosis levels remained unchanged during oncogenesis.
Conclusions:
- Diabetes mellitus appears to promote oral oncogenesis by enhancing cell proliferation via the Ras/Raf/MAPK pathway.
- The findings support diabetes as a risk factor for OSCC development.
- Further research into therapeutic strategies targeting these pathways in diabetic patients is warranted.
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