Widespread expression of Sonic hedgehog (Shh) and Nrf2 in patients treated with cisplatin predicts outcome in resected tumors and are potential therapeutic targets for HPV-negative head and neck cancer. (March 2020)

• Record Type: Journal Article
• Authors: Noman, Abu Shadat M.; Parag, Rashed R.; Rashid, Muhammad I.; Rahman, Mohammad Z.; Chowdhury, Ali A.; Sultana, Afrin; Jerin, Chandsultana; Siddiqua, Ayesha; Rahman, Lutfur; Shirin, Afsana; Nayeem, Junayed; Mahmud, Reaz; Akther, Sonam; Shil, Rajib K.; Hossain, Ikram; Alam, Sharmin; Chowdhury, Arfina; Basher, Shabnam B.; Hasan, Abul; Bithy, Shammy; Aklima, Jannatul; Rahman, Mizanur; Chowdhury, Nabila; Banu, Tahmina; Karakas, Bedri; Yeger, Herman; Farhat, Walid A.; Islam, Syed S.
• Is Part Of: Therapeutic advances in medical oncology. Volume 12(2020)
• Publication Date: 2020-03
• Subjects: cisplatin -- disease-free survival -- HNSCC -- Nrf2 -- overall survival -- Shh; Oncology -- Periodicals; Cancer -- Treatment -- Periodicals; 616.994005
• DOI: 10.1177/1758835920911229
• Languages: English
• ISSNs: 1758-8340

Abstract

Background: Sonic hedgehog (Shh) and Nrf2 play a critical role in chemotherapeutic resistance. These two genes have been found to be dysregulated in head and neck squamous cell carcinomas (HNSCC). The purpose of this study was to analyze the expression, function and clinical prognostic relationship of Shh and Nrf2 in HNSCC in the context of therapeutic resistance and cancer stem cells (CSCs). Methods: We analyzed a cohort of patients with HNSCC to identify potential therapeutic biomarkers correlating with overall survival (OS) as well as disease-free survival (DFS) from our own data and validated these results using The Cancer Genome Atlas dataset. Expression of Shh and Nrf2 was knocked down by siRNA and cell growth, sphere growth and chemotherapeutic resistance were evaluated. Results: Widespread abundant expression of Shh and Nrf2 proteins were associated with shorter OS and DFS. The combination of Shh and Nrf2 expression levels was found to be a significant predictor of patient DFS. The tumor stromal index was correlated with Shh expression and inversely associated with shorter OS and DFS. Inhibition of Shh by siRNA or cyclopamine resulted in the attenuation of resistant CSC self-renewal, invasion, clonogenic growth and re-sensitization to the chemotherapeutic agents. Concomitant upregulation of Shh and Nrf2 proved to be an independent predictor of poor OS and DFS in patients with HNSCC. Conclusions: These findings suggest that Shh and Nrf2 could serve as therapeutic targets as well as promising dual prognostic therapeutic biomarkers for HNSCC.