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蛇毒,一种黑色素瘤的潜在治疗方法。一项系统综述。

Snake venom, a potential treatment for melanoma. A systematic review.

作者信息

Bialves Tatiane Senna, Bastos Junior Claudio L Q, Cordeiro Marcos Freitas, Boyle Robert Tew

机构信息

Programa de Pós-Graduação em Ciências Fisiológicas (PPGCF), Universidade Federal do Rio Grande - FURG, Av. Itália, s/n - km 8 - Carreiros, Rio Grande, Rio Grande do Sul, Brazil.

Programa de Pós-Graduação em Ciências Fisiológicas (PPGCF), Universidade Federal do Rio Grande - FURG, Av. Itália, s/n - km 8 - Carreiros, Rio Grande, Rio Grande do Sul, Brazil.

出版信息

Int J Biol Macromol. 2023 Mar 15;231:123367. doi: 10.1016/j.ijbiomac.2023.123367. Epub 2023 Jan 21.

Abstract

Despite advances in treating patients with melanoma, there are still many treatment challenges to overcome. Studies with snake venom-derived proteins/peptides describe their binding potential, and inhibition of some proliferative mechanisms in melanoma. The combined use of these compounds with current therapies could be the strategic gap that will help us discover more effective treatments for melanoma. The present study aimed to carry out a systematic review identifying snake venom proteins and peptides described in the literature with antitumor, antimetastatic, or antiangiogenic effects on melanoma and determine the mechanisms of action that lead to these anti-tumor effects. Snake venoms contain proteins and peptides which are antiaggregant, antimetastatic, and antiangiogenic. The in vivo results are encouraging, considering the reduction of metastases and tumor size after treatment. In addition to these results, it was reported that these venom compounds could act in combination with chemotherapeutics (Acurhagin-C; Macrovipecetin), sensitizing and preparing tumor cells for treatment. There is a consensus that snake venom is a promising strategy for the improvement of antimelanoma therapies, but it has been little explored in the current context, combined with inhibitors, immunotherapy or tumor microenvironment, for example. We suggest Lebein as a candidate for combination therapy with BRAF inhibitors.

摘要

尽管在黑色素瘤患者的治疗方面取得了进展,但仍有许多治疗挑战需要克服。对蛇毒衍生的蛋白质/肽的研究描述了它们的结合潜力,以及对黑色素瘤某些增殖机制的抑制作用。将这些化合物与当前疗法联合使用可能是一个战略突破点,有助于我们发现更有效的黑色素瘤治疗方法。本研究旨在进行一项系统综述,识别文献中描述的对黑色素瘤具有抗肿瘤、抗转移或抗血管生成作用的蛇毒蛋白和肽,并确定导致这些抗肿瘤作用的作用机制。蛇毒含有具有抗聚集、抗转移和抗血管生成作用的蛋白质和肽。考虑到治疗后转移和肿瘤大小的减少,体内结果令人鼓舞。除了这些结果外,还报道了这些毒液化合物可与化疗药物(Acurhagin-C;Macrovipecetin)联合作用,使肿瘤细胞对治疗敏感并做好准备。人们普遍认为蛇毒是改善抗黑色素瘤治疗的一种有前途的策略,但在当前背景下,与抑制剂、免疫疗法或肿瘤微环境等联合使用的探索还很少。我们建议将Lebein作为与BRAF抑制剂联合治疗的候选药物。

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