| Literature DB >> 32990596 |
Pei San Yee1, Stacey Price2, Annie Wai Yeeng Chai1, Shi Mun Yee1, Hui Mei Lee1, Vivian Kh Tiong1, Emanuel Gonçalves2, Fiona M Behan2, Jessica Bateson2, James Gilbert2, Aik Choon Tan3, Ultan McDermott4, Mathew J Garnett2, Sok Ching Cheong1,5.
Abstract
New therapeutic targets for oral squamous cell carcinoma (OSCC) are urgently needed. We conducted genome-wide CRISPR-Cas9 screens in 21 OSCC cell lines, primarily derived from Asians, to identify genetic vulnerabilities that can be explored as therapeutic targets. We identify known and novel fitness genes and demonstrate that many previously identified OSCC-related cancer genes are non-essential and could have limited therapeutic value, while other fitness genes warrant further investigation for their potential as therapeutic targets. We validate a distinctive dependency on YAP1 and WWTR1 of the Hippo pathway, where the lost-of-fitness effect of one paralog can be compensated only in a subset of lines. We also discover that OSCCs with WWTR1 dependency signature are significantly associated with biomarkers of favorable response toward immunotherapy. In summary, we have delineated the genetic vulnerabilities of OSCC, enabling the prioritization of therapeutic targets for further exploration, including the targeting of YAP1 and WWTR1.Entities:
Keywords: CRISPR screen; Hippo pathway; cancer biology; fitness genes; genetics; genomics; human; oral squamous cell carcinoma; therapeutic targets
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Year: 2020 PMID: 32990596 PMCID: PMC7591259 DOI: 10.7554/eLife.57761
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140