Department of Oncogene Regulation, Chittaranjan National Cancer Institute, 37, S.P. Mukherjee Road, Kolkata, West Bengal, 700026, India.
Department of Surgical Oncology, Chittaranjan National Cancer Institute, 37, S.P. Mukherjee Road, Kolkata, West Bengal, 700026, India.
Med Microbiol Immunol. 2021 Feb;210(1):49-63. doi: 10.1007/s00430-020-00697-9. Epub 2020 Nov 23.
The aim of this study is to understand the association of HPV infection and wnt-β-catenin self-renewal pathway in development of head and neck squamous cell carcinoma (HNSCC). For this reason, the molecular profiles (methylation/deletion/expression) of antagonists (SFRP1/2 and DKK1), agonists (FZD7 and LRP6) and effector protein β-catenin of the pathway were analyzed in HPV positive/negative oral epithelium at first, followed by its changes during development of the tumor along with correlations with different clinico-pathological parameters. HPV infection alone or in combination with tobacco habit could activate p- β-catenin expression in basal/parabasal layers of oral epithelium through high expression of FZD7 and significant down regulation of SFRP1/2 through promoter hypermethylation due to over expression of DNMT1 with ubiquitous down regulation of DKK1 and up-regulation of LRP6. This phenomenon has been seen in respective HPV positive and negative HNSCC tumors with additional deletion/microsatellite size alterations in the antagonists. Overall alterations (methylation/deletion) of SFRP1/2, DKK1 gradually increased from Group I (HPV-/Tobacco-) to Group IV(HPV+/Tobacco+) tumors, leading to the worst prognosis of the patients. Thus, the transmission of differentially activated wnt-β-catenin pathway from HPV positive/negative basal/parabasal layers of oral epithelium to HNSCC tumors determines differences in molecular pathogenesis of the disease.
本研究旨在探讨 HPV 感染与 wnt-β-连环蛋白自我更新通路在头颈部鳞状细胞癌(HNSCC)发生发展中的相关性。为此,我们首先分析了 HPV 阳性/阴性口腔上皮中该通路的拮抗剂(SFRP1/2 和 DKK1)、激动剂(FZD7 和 LRP6)和效应蛋白β-连环蛋白的分子谱(甲基化/缺失/表达),然后分析了其在肿瘤发生过程中的变化,并与不同的临床病理参数进行了相关性分析。HPV 感染单独或与烟草习惯联合作用可通过高表达 FZD7 和启动子超甲基化导致 SFRP1/2 显著下调,从而激活口腔上皮基底层/副基底层中 p- β-连环蛋白的表达,DNMT1 的过表达导致 DKK1 的普遍下调和 LRP6 的上调。这种现象在各自的 HPV 阳性和阴性 HNSCC 肿瘤中都可以看到,拮抗剂中存在缺失/微卫星大小改变。SFRP1/2、DKK1 的总体改变(甲基化/缺失)从 I 组(HPV-/烟草-)逐渐增加到 IV 组(HPV+/烟草+)肿瘤,导致患者预后最差。因此,从 HPV 阳性/阴性口腔上皮基底层/副基底层到 HNSCC 肿瘤中差异激活的 wnt-β-连环蛋白通路的传递决定了该疾病分子发病机制的差异。