Effect of the topical administration of N-(2-(4-bromophenylamino)-5-(trifluoromethyl)phenyl)nicotinamide compound in a murine subcutaneous melanoma model

烟酰胺 细胞凋亡 药理学 黑色素瘤 皮下注射 医学 毒性 化学 癌症研究 内科学 生物化学
作者
Juliana A. Vale,Ana Paula Martins de Souza,Graziela Domingues de Almeida Lima,Victor Gonçalves,Guilherme Musse Moreira,Marcus Vinícius de Andrade Barros,Wagner Luiz Pereira,Nara Clara Lazaroni E Merchid,Juliana Lopes Rangel Fietto,Gustavo Costa Bressan,Róbson Ricardo Teixeira,Mariana Machado‐Neves
出处
期刊:Anti-Cancer Drugs [Lippincott Williams & Wilkins]
卷期号:31 (7): 718-727 被引量:3
标识
DOI:10.1097/cad.0000000000000944
摘要

Conventional treatments for metastatic melanomas are still ineffective and generate numerous side effects, justifying the search for new therapies. The antimetastatic effect of the named N-(2-(4-bromophenylamino)-5-(trifluoromethyl)phenyl)nicotinamide (SRVIC30) compound has been previously demonstrated in murine melanoma. Herein, we aimed to evaluate its effect when topically administrated in a murine subcutaneous melanoma model. For that, mice C57BL/6 were injected subcutaneously with 2 × 10 5 B16-F10 cells. Topical treatment began when tumors became visible on animal’s back. Therefore, tumor volume was measured three times a week until it reaches 12 mm 3 approximately. At this point, 40 mg oil-in-water cream (Lanette) without (control mice; n = 10) or with SRVIC30 compound (SRVIC30 group; n = 10 animals) were spread daily over the tumor external surface using a small brush for 14 days. The treatments increased the percentage of peroxidase antioxidant enzyme and dead cells via caspase-3 activation, with a consequent deposit of collagen fibers in the tumors. In addition, the skin of treated animals showed the presence of inflammatory infiltrate. Finally, SRVIC30 did not show signs of toxicity. Thus, we concluded that the topic administration of SRVIC30 was able to influence crucial anticancer processes such as tumor cells apoptosis and surrounding microenvironment.

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