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Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers.

Authors :
Smith-Byrne, Karl
Hedman, Åsa
Dimitriou, Marios
Desai, Trishna
Sokolov, Alexandr V.
Schioth, Helgi B.
Koprulu, Mine
Pietzner, Maik
Langenberg, Claudia
Atkins, Joshua
Penha, Ricardo Cortez
McKay, James
Brennan, Paul
Sirui Zhou
Richards, Brent J.
Yarmolinsky, James
Martin, Richard M.
Borlido, Joana
Mu, Xinmeng J.
Butterworth, Adam
Source :
Nature Communications; 4/29/2024, Vol. 15 Issue 1, p1-11, 11p
Publication Year :
2024

Abstract

Circulating proteins can reveal key pathways to cancer and identify therapeutic targets for cancer prevention. We investigate 2,074 circulating proteins and risk of nine common cancers (bladder, breast, endometrium, head and neck, lung, ovary, pancreas, kidney, and malignant non-melanoma) using cis protein Mendelian randomisation and colocalization. We conduct additional analyses to identify adverse side-effects of altering risk proteins and map cancer risk proteins to drug targets. Here we find 40 proteins associated with common cancers, such as PLAUR and risk of breast cancer [odds ratio per standard deviation increment: 2.27, 1.88-2.74], and with high-mortality cancers, such as CTRB1 and pancreatic cancer [0.79, 0.73-0.85]. We also identify potential adverse effects of protein-altering interventions to reduce cancer risk, such as hypertension. Additionally, we report 18 proteins associated with cancer risk that map to existing drugs and 15 that are not currently under clinical investigation. In sum, we identify protein-cancer links that improve our understanding of cancer aetiology. We also demonstrate that the wider consequence of any protein-altering intervention on well-being and morbidity is required to interpret any utility of proteins as potential future targets for therapeutic prevention. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
178176222
Full Text :
https://doi.org/10.1038/s41467-024-46834-3