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The Cancer Surfaceome Atlas integrates genomic, functional and drug response data to identify actionable targets.


ABSTRACT: Cell-surface proteins (SPs) are a rich source of immune and targeted therapies. By systematically integrating single-cell and bulk genomics, functional studies and target actionability, in the present study we comprehensively identify and annotate genes encoding SPs (GESPs) pan-cancer. We characterize GESP expression patterns, recurrent genomic alterations, essentiality, receptor-ligand interactions and therapeutic potential. We also find that mRNA expression of GESPs is cancer-type specific and positively correlates with protein expression, and that certain GESP subgroups function as common or specific essential genes for tumor cell growth. We also predict receptor-ligand interactions substantially deregulated in cancer and, using systems biology approaches, we identify cancer-specific GESPs with therapeutic potential. We have made this resource available through the Cancer Surfaceome Atlas ( http://fcgportal.org/TCSA ) within the Functional Cancer Genome data portal.

SUBMITTER: Hu Z 

PROVIDER: S-EPMC9940627 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature

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The Cancer Surfaceome Atlas integrates genomic, functional and drug response data to identify actionable targets.

Hu Zhongyi Z   Yuan Jiao J   Long Meixiao M   Jiang Junjie J   Zhang Youyou Y   Zhang Tianli T   Xu Mu M   Fan Yi Y   Tanyi Janos L JL   Montone Kathleen T KT   Tavana Omid O   Chan Ho Man HM   Hu Xiaowen X   Vonderheide Robert H RH   Zhang Lin L  

Nature cancer 20211213 12


Cell-surface proteins (SPs) are a rich source of immune and targeted therapies. By systematically integrating single-cell and bulk genomics, functional studies and target actionability, in the present study we comprehensively identify and annotate genes encoding SPs (GESPs) pan-cancer. We characterize GESP expression patterns, recurrent genomic alterations, essentiality, receptor-ligand interactions and therapeutic potential. We also find that mRNA expression of GESPs is cancer-type specific and  ...[more]

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