Laboratorio de Biomedicina Molecular, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo, México.
CONACyT- Universidad Autónoma de Guerrero, Chilpancingo, México.
Cancer Genomics Proteomics. 2021 May-Jun;18(3):273-283. doi: 10.21873/cgp.20258. Epub 2021 Apr 23.
BACKGROUND/AIM: The E6 genotypic variants of HPV 16 identified in lesions of women with cervical cancer (CC) in Southern of Mexico include the E-G350, AAa, AAc, E-C188/G350, and E-A176/G350, transcriptomic analysis cells transfected with those variants showed to induce differential expression of the host genes involved in the development of CC, the aim of this work was to understand how the over-expression of the E6 oncoprotein and its variants can induce molecular mechanisms that lead to more aggressive HPV 16 phenotypes in cervical cancer and which proteins could be associated with the process.
Total extracts from C33A, C33A mock, C33A AAa, C33A E-C188/G350, C33A E-A176/G350, and C33A E-prototype cells were analyzed using 2D electrophoresis, PDQuest software and mass spectrometry, validation of results was performed through qPCR.
Statistically significant differential expression of 122 spots was detected, 12 of the identified proteins were associated with metabolism and metabolic programming. Out of these CCT8, ENO and ALDH1A were further validated.
CCT8 and ALDH1A were found to be over-expressed in C33A AAa and C33A E-A176/G350, compared to the E prototype. Both proteins could be associated with a most aggressive phenotype due to their relationship with metabolism, protein folding and stemness, mechanisms associated to E6 that could be useful in the design of new therapies.
背景/目的:在墨西哥南部宫颈癌(CC)病变中鉴定的 HPV 16 的 E6 基因型变体包括 E-G350、AAa、AAc、E-C188/G350 和 E-A176/G350。转染这些变体的细胞的转录组分析显示,诱导了与 CC 发展相关的宿主基因的差异表达。本工作的目的是了解 E6 癌蛋白及其变体的过表达如何诱导导致 HPV 16 表型更具侵袭性的分子机制,以及哪些蛋白质可能与该过程相关。
使用 2D 电泳、PDQuest 软件和质谱分析 C33A、C33A 模拟、C33A AAa、C33A E-C188/G350、C33A E-A176/G350 和 C33A E-原型细胞的总提取物。通过 qPCR 验证结果。
检测到 122 个斑点的差异表达具有统计学意义,鉴定的 12 种蛋白质与代谢和代谢编程有关。其中 CCT8、ENO 和 ALDH1A 进一步得到验证。
与 E 原型相比,在 C33A AAa 和 C33A E-A176/G350 中发现 CCT8 和 ALDH1A 过表达。由于它们与代谢、蛋白质折叠和干性的关系,这两种蛋白质都可能与更具侵袭性的表型相关,这些与 E6 相关的机制可能有助于设计新的治疗方法。