Waterpipe smoke condensate induces epithelial-mesenchymal transformation and promotes metastasis of oral cancer by FOXD1 expression

被引:2
|
作者
Prasad, Prathibha [1 ,2 ,3 ]
Kannan, Balachander [4 ]
Sriram, Gopu [5 ]
Jaber, Mohamed [1 ,3 ]
Khair, Al Moutassem Billah [1 ,3 ]
Ramasubramanian, Abilasha [2 ]
Ramani, Pratibha [2 ]
Jayaseelan, Vijayashree Priyadharshini [6 ]
Arumugam, Paramasivam [4 ]
机构
[1] Ajman Univ, Med & Dent Sci Dept, Coll Dent, Ctr Med & Bioallied Hlth Sci Res, Ajman, U Arab Emirates
[2] Saveetha Univ, Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci SIMATS, Dept Oral Pathol, Chennai, India
[3] Ajman Univ, Ctr Med & Bioallied Hlth Sci Res, Ajman, U Arab Emirates
[4] Saveetha Univ, Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci SIMATS, Ctr Cellular & Mol Res,Mol Biol Lab, Chennai 600077, India
[5] Natl Univ Singapore, Fac Dent, Singapore, Singapore
[6] Saveetha Univ, Saveetha Inst Med & Tech Sci SIMATS, Saveetha Dent Coll & Hosp, Clin Genet Lab,Ctr Cellular & Mol Res, Chennai, India
关键词
Foxd1; Oral squamous cell carcinoma; Waterpipe smoke condensate; Epithelial-mesenchymal transition; Cancer progression; Therapeutic target; PROLIFERATION; SUPPRESSES; PROGNOSIS; CELLS;
D O I
10.1016/j.jormas.2024.101900
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background/purpose: Smoking is a major contributor to global oral cancer cases, necessitating urgent intervention. FOXD1, involved in developmental processes and various cancers, shows promise as a prognostic marker in oral squamous cell carcinoma (OSCC). This study investigates the impact of waterpipe smoke condensate (WPSC) on OSCC, focusing on FOXD1 role in inducing epithelial-mesenchymal transition (EMT) and metastasis. Methods: The study involved using OSCC cells treated with WPSC to evaluate their proliferation, colony formation, gene expression, and protein levels. The researchers also explored the clinical relevance of their findings using online databases to analyze FOXD1 expression in cancer tissues and its correlation with clinicopathological features and patient survival. Additionally, in silico tools were employed for functional analysis, pathway enrichment, and network exploration. Results: The study found that WPSC increased the expression of FOXD1 in OSCC cells, which led to increased cell growth. The study also showed that FOXD1 plays a critical role in the EMT process induced by WPSC, as evidenced by changes in the expression of EMT-related genes and proteins. Clinical analysis revealed that FOXD1 was significantly associated with more aggressive tumor features and poorer prognosis in cancer patients. Conclusion: The study highlights FOXD1 as a key player in OSCC pathogenesis and a potential prognostic marker and therapeutic target, particularly when influenced by WPSC exposure. Further research is needed to explore FOXD1 molecular mechanisms and clinical implications to enhance OSCC treatment strategies. (c) 2024 Elsevier Masson SAS. All rights reserved.
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页数:9
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