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

Author:

Noman Abu Shadat M.12,Parag Rashed R.1,Rashid Muhammad I.1,Rahman Mohammad Z.3,Chowdhury Ali A.4,Sultana Afrin1,Jerin Chandsultana1ORCID,Siddiqua Ayesha1,Rahman Lutfur1,Shirin Afsana1,Nayeem Junayed1,Mahmud Reaz1,Akther Sonam1,Shil Rajib K.1,Hossain Ikram1,Alam Sharmin1,Chowdhury Arfina1,Basher Shabnam B.1,Hasan Abul1,Bithy Shammy1,Aklima Jannatul1,Rahman Mizanur15,Chowdhury Nabila1,Banu Tahmina6,Karakas Bedri7,Yeger Herman8,Farhat Walid A.9,Islam Syed S.10ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, The University of Chittagong, Chittagong, Bangladesh

2. Department of Pathology, McGill University, Montreal, Quebec, Canada

3. Department of Pathology, Chittagong Medical College and Hospital, Chittagong, Bangladesh

4. Department of Radiotherapy, Chittagong Medical College and Hospital, Chittagong, Bangladesh

5. Rangamati Medical College, Rangamati, Bangladesh

6. Chittagong Research Institute of Children Surgery, Chittagong, Bangladesh

7. Department of Molecular Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia

8. Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada

9. Department of Urology, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA

10. Department of Molecular Oncology, Cancer Biology and Experimental Therapeutics, King Faisal Specialist Hospital and Research Centre, School of Medicine, Alfaisal University, Thakassussi Street, Riyadh, 11211, Saudi Arabia

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.

Publisher

SAGE Publications

Subject

Oncology

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