Molecular Markers of Angiogenesis and Metastasis in Lines of Oral Carcinoma after Treatment with Melatonin

被引:43
作者
Goncalves, Naiane do Nascimento [1 ,2 ]
Rodrigues, Rodrigo Ventura [1 ,3 ]
Jardim-Perassi, Bruna Victorasso [1 ,3 ]
Moschetta, Marina Gobbe [1 ,2 ]
Lopes, Juliana Ramos [1 ,3 ]
Colombo, Jucimara [1 ]
Pires de Campos Zuccari, Debora Aparecida [1 ,4 ,5 ]
机构
[1] FAMERP, Fac Medicina Sao Jose Do Rio Preto, LIMC, BR-15090000 Sao Jose Do Rio Preto, SP, Brazil
[2] FAMERP, Fac Med Sao Jose do Rio Preto, PostGrad Program Hlth Sci, BR-15090000 Sao Jose Do Rio Preto, SP, Brazil
[3] Univ Estadual Paulista, UNESP IBILCE, PostGrad Program Genet, BR-15054000 Sao Jose Do Rio Preto, SP, Brazil
[4] FAMERP, Dept Mol Biol, BR-15090000 Sao Jose Do Rio Preto, SP, Brazil
[5] UNESP IBILCE, Program Post Grad Genet, Sao Jose Do Rio Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Cell lines; HIF-1; alpha; ROCK-1; melatonin; oral cancer; VEGF; RHO-KINASE; CYTOSKELETAL DYNAMICS; SYNOVIAL MACROPHAGES; RHO/ROCK PATHWAY; VEGF EXPRESSION; CELL-MIGRATION; NECK-CANCER; HIF-1-ALPHA; INHIBITION; ROCK1;
D O I
10.2174/1871520614666140812110246
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Oral cancer is the most common type of head and neck cancer and its high rate of mortality and morbidity is closely related to the processes of angiogenesis and tumor metastasis. The overexpression of the pro-angiogenic genes, HIF-1 alpha and VEGF, and pro-metastatic gene, ROCK-1, are associated with unfavorable prognosis in oral carcinoma. Melatonin has oncostatic, antiangiogenic and antimetastatic properties in several types of neoplasms, although its relationship with oral cancer has been little explored. This study aims to analyze the expression of the genes HIF-1 alpha, VEGF and ROCK-1 in cell lines of squamous cell carcinoma of the tongue, after treatment with melatonin. Methods: SCC9 and SCC25 cells were cultured and cell viability was assessed by MTT assay, after treatment with 100 mu M of CoCl2 to induce hypoxia and with melatonin at different concentrations. The analysis of quantitative RT-PCR and the immunocytochemical analysis were performed to verify the action of melatonin under conditions of normoxia and hypoxia, on gene and protein expression of HIF-1 alpha, VEGF and ROCK-1. Results: The MTT assay showed a decrease in cell viability in both cell lines, after the treatment with melatonin. The analysis of quantitative RT-PCR indicated an inhibition of the expression of the pro-angiogenic genes HIF-1 alpha (P < 0.001) and VEGF (P < 0.001) under hypoxic conditions, and of the pro-metastatic gene ROCK-1 (P < 0.0001) in the cell line SCC9, after treatment with 1 mM of melatonin. In the immunocytochemical analysis, there was a positive correlation with gene expression data, validating the quantitative RT-PCR results for cell line SCC9. Treatment with melatonin did not demonstrate inhibition of the expression of genes HIF-1 alpha, VEGF and ROCK-1 in line SCC25, which has different molecular characteristics and greater degree of malignancy when compared to the line SCC9. Conclusion: Melatonin affects cell viability in the SCC9 and SCC25 lines and inhibits the expression of the genes HIF-1 alpha, VEGF and ROCK-1 in SCC9 line. Additional studies may confirm the potential therapeutic effect of melatonin in some subtypes of oral carcinoma.
引用
收藏
页码:1302 / 1311
页数:10
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