Genistein anticancer efficacy during induced oral squamous cell carcinoma: an experimental study

• Published in: Journal of Egyptian National Cancer Institute Vol. 34; no. 1; pp. 1 - 10
• Main Authors: Hussein, Ahmed M., Attaai, Abdelraheim H., Zahran, Asmaa M.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 05.09.2022; Springer; SpringerOpen
• Subjects: Analysis; Angiogenesis inhibitors; Apoptosis; Cancer; Care and treatment; DNA ploidy; Drug therapy; Flow cytometry; Genistein; Hamsters; Isoflavones; Medicine; Medicine & Public Health; Oncology; Petroleum products; Physiological aspects; Prevention; S-phase fraction; Squamous cell carcinoma; Egypt; DNA ploidy; Flow cytometry; S-phase fraction; Genistein
• ISSN: 1110-0362; 2589-0409
• DOI: 10.1186/s43046-022-00140-5

Background About 7 million people die from various types of cancer every year representing nearly 12.5% of deaths worldwide. This fact raises the demand to develop new, effective anticancer, onco-suppressive, and chemoprotective agents for the future fighting of cancers. Genistein exhibits pleiotropic functions in cancer, metabolism, and inflammation. It functions as an antineoplastic agent through its effect on the cell cycle, apoptotic processes, angiogenesis, invasion, and metastasis. Aim of the study The current study aimed to study the genistein onco-suppressive effects during 7,12-dimethylbenz[a]anthracene (DMBA)-induced oral carcinogenesis in hamsters’ buccal pouch utilizing flow cytometry analysis (FMA), as a fast-diagnosing tool, in addition to the histopathology. Material and methods The buccal mucosa of adult male Syrian hamsters was painted with paraffin oil only (group 1), DMBA mixed in mineral oil (group 2), or orally administrated genistein along with painting DMBA (group 2B). The buccal mucosa was utilized for flow cytometric analysis and histopathological examination. Results Grossly, DMBA-induced carcinogenesis started at the 9th week. Progressive signs appeared in the following weeks reaching to large ulcerative oral masses and exophytic nodules at the 21st week. Histologically, invasive well-differentiated oral squamous cell carcinoma (OSCC) appeared in the underlying tissues from the 12th week, showing malignant criteria. Genistein had delayed clinicopathological change, which started 6 weeks later, than the DMBA-painted hamsters, as mild epithelial dysplastic changes. This became moderate during the last 6 weeks, without dysplastic changes. Flow cytometry revealed that DMBA led to considerable variation in DNA proliferation activity, aneuploid DNA pattern, in 47.22% of hamsters and significantly raised the S-phase fragment (SPF) values, which drastically reduced after genistein treatment. Conclusion Taken together, genistein could be employed as an onco-suppressive agent for carcinogenesis. Moreover, FMA could be used as an aiding fast tool for diagnosis of cancer.