| Literature DB >> 28469960 |
Akihito Arai1, Tokuhiro Chano2, Kaichiro Ikebuchi3, Yusuke Hama2, Yasuko Ochi1, Hitosuke Tameno1, Taketoshi Shimada4.
Abstract
Hypopharyngeal carcinoma is one of the worst prognostic malignancies among head and neck carcinomas. Therefore, a good biomarker should be identified to predict the best therapeutic option before starting the treatment. In cell models, p62/SQSTM1 levels affected the Nrf2-Keap1 pathway, ROS levels, GSH/GSSG ratios and cell growth, especially under irradiation rather than under CDDP exposure, which was toxic despite p62/SQSTM1 status. In a clinical cohort of hypopharyngeal carcinomas, high levels of p62/SQSTM1 significantly predicted poor prognosis (log-rank test, Chi-square value = 6.750, P = 0.0094) and maximum critical risk (Cox proportional hazard ratio = 4.405, P = 0.0086), especially in the radiotherapy group. Therefore, when p62/SQSTM1 is elevated in the biopsy section, hypopharyngeal carcinoma should be treated with surgical and/or chemotherapeutic options.Entities:
Keywords: head and neck cancer; hypopharyngeal carcinoma; p62/SQSTM1; radiotherapy resistance
Year: 2017 PMID: 28469960 PMCID: PMC5411795
Source DB: PubMed Journal: Am J Cancer Res ISSN: 2156-6976 Impact factor: 6.166