Laboratorio de Química Analítica para Investigación y Desarrollo (QUIANID), Instituto Interdisciplinario de Ciencias Básicas, Universidad Nacional de Cuyo, CONICET, Facultad de Ciencias Exactas y Naturales, Padre J. Contreras 1300, 5500, Mendoza, Argentina; Facultad de Farmacia y Bioquímica, Universidad Juan Agustín Maza, Lateral Sur del Acceso Este 2245, M5519, Guaymallén, Mendoza, Argentina.
Laboratorio de Química Analítica para Investigación y Desarrollo (QUIANID), Instituto Interdisciplinario de Ciencias Básicas, Universidad Nacional de Cuyo, CONICET, Facultad de Ciencias Exactas y Naturales, Padre J. Contreras 1300, 5500, Mendoza, Argentina.
J Trace Elem Med Biol. 2020 Mar;58:126441. doi: 10.1016/j.jtemb.2019.126441. Epub 2019 Nov 23.
The interest in inorganic Hg toxicity and carcinogenicity has been pointed to target organs such as kidney, brain or placenta, but only a few studies have focused on the mammary gland. In this work, analytical combination techniques (SDS-PAGE followed by CV-AFS, and nanoUPLC-ESI-MS/MS) were used to determine proteins that could bind Hg in three human mammary cell lines. Two of them were tumorigenic (MCF-7 and MDA-MB-231) and the other one was the non-tumorigenic cell line (MCF-10A). There are no studies that provide this kind of information in breast cell lines with IHg treatment. Previously, we described the viability, uptake and the subcellular distribution of Hg in human breast cells and analysis of RNA-seq about the genes that encode proteins which are related to cytotoxicity of Hg. This work provides important protein candidates for further studies of Hg toxicity in the mammary gland, thus expanding our understanding of how environmental contaminants might affect tumor progression and contribute with future therapeutic methods.
人们对无机汞的毒性和致癌性的兴趣已经指向了肾脏、大脑或胎盘等靶器官,但只有少数研究关注于乳腺。在这项工作中,分析组合技术(SDS-PAGE 后接 CV-AFS 和 nanoUPLC-ESI-MS/MS)被用于确定三种人乳腺细胞系中可以与汞结合的蛋白质。其中两种是致瘤性的(MCF-7 和 MDA-MB-231),另一种是非致瘤性细胞系(MCF-10A)。在接受 IHg 处理的乳腺细胞系中,尚无研究提供此类信息。此前,我们描述了人乳腺细胞中 Hg 的活力、摄取和亚细胞分布,以及与 Hg 细胞毒性相关的编码蛋白的 RNA-seq 分析。这项工作为进一步研究汞在乳腺中的毒性提供了重要的候选蛋白,从而扩展了我们对环境污染物如何影响肿瘤进展的理解,并为未来的治疗方法提供了帮助。