Palumbo Júnior Antonio, Da Costa Nathalia Meireles, Esposito Francesco, Fusco Alfredo, Pinto Luis Felipe Ribeiro
a Programa de Carcinogênese Molecular, Instituto Nacional de Câncer - INCA, Rua André Cavalcanti , Rio de Janeiro , RJ , Brazil.
b Laboratório de Interações Celulares, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro Prédio de Ciências da Saúde - Cidade Universitária, Ilha do Fundão, A. Carlos Chagas , Rio de Janeiro , RJ , Brasil.
Cell Cycle. 2016 Sep 16;15(18):2410-3. doi: 10.1080/15384101.2016.1215388. Epub 2016 Aug 2.
We have recently shown that HMGA2 is overexpressed in esophageal squamous cell carcinoma (ESCC) and its detection allows to discriminate between cancer and normal surrounding tissue proposing HMGA2 as a novel diagnostic marker. Interestingly, esophageal adenocarcinoma shows an opposite behavior with the overexpression of HMGA1 but not HMGA2. Moreover, we show that the suppression of HMGA2 in 2 ESCC cell lines reduces the malignant phenotype. Then, this paper highlights a differential induction of the HMGA proteins, depending on the cancer histological type, and reinforces the perspective of an innovative esophageal cancer therapy based on the suppression of the HMGA protein function and/or expression.
我们最近发现,HMGA2在食管鳞状细胞癌(ESCC)中过度表达,检测该蛋白有助于区分癌组织与周围正常组织,这表明HMGA2可作为一种新型诊断标志物。有趣的是,食管腺癌却呈现相反的情况,即HMGA1过度表达而HMGA2未过度表达。此外,我们发现抑制两种ESCC细胞系中的HMGA2可降低其恶性表型。因此,本文强调了HMGA蛋白的诱导存在差异,这取决于癌症的组织学类型,并强化了基于抑制HMGA蛋白功能和/或表达的创新性食管癌治疗前景。