TMEM16A/ANO1 inhibits apoptosis via downregulation of Bim expression

Neal R. Godse, Nayel Khan, Zachary A. Yochum, Roberto Gomez-Casal, Carolyn Kemp, Daniel J. Shiwarski, Raja S. Seethala, Scott Kulich, Mukund Seshadri, Timothy F. Burns, Umamaheswar Duvvuri

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

Purpose: TMEM16A is a calcium-activated chloride channel that is amplified in a variety of cancers, including 30% of head and neck squamous cell carcinomas (HNSCCs), raising the possibility of an anti-apoptotic role in malignant cells. This study investigated this using a multimodal, translational investigation. Experimental Design: Combination of (i) in vitro HNSCC cell culture experiments assessing cell viability, apoptotic activation, and protein expression (ii) in vivo studies assessing similar outcomes, and (iii) molecular and staining analysis of human HNSCC samples. Results: TMEM16A expression was found to correlate with greater tumor size, increased Erk 1/2 activity, less Bim expression, and less apoptotic activity overall in human HNSCC. These findings were corroborated in subsequent in vitro and in vivo studies and expanded to include a cisplatin-resistant phenotype with TMEM16A overexpression. A cohort of 41 patients with laryngeal cancer demonstrated that cases that recurred after chemoradiation failure were associated with a greater TMEM16A overexpression rate than HNSCC that did not recur. Conclusions: Ultimately, this study implicates TMEM16A as a contributor to tumor progression by limiting apoptosis and as a potential biomarker of more aggressive disease.

Original languageEnglish (US)
Pages (from-to)7324-7332
Number of pages9
JournalClinical Cancer Research
Volume23
Issue number23
DOIs
StatePublished - Dec 1 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
©2017 AACR.

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