CETSA interaction proteomics define specific RNA-modification pathways as key components of fluorouracil-based cancer drug cytotoxicity

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CETSA interaction proteomics define specific RNA-modification pathways as key components of fluorouracil-based cancer drug cytotoxicity
Title:
CETSA interaction proteomics define specific RNA-modification pathways as key components of fluorouracil-based cancer drug cytotoxicity
Journal Title:
Cell Chemical Biology
Publication Date:
14 July 2021
Citation:
Liang, Y. Y., Bacanu, S., Sreekumar, L., Ramos, A. D., Dai, L., Michaelis, M., … Nordlund, P. (2021). CETSA interaction proteomics define specific RNA-modification pathways as key components of fluorouracil-based cancer drug cytotoxicity. Cell Chemical Biology. doi:10.1016/j.chembiol.2021.06.007
Abstract:
The optimal use of many cancer drugs is hampered by a lack of detailed understanding of their mechanism of action (MoA). Here, we apply a high-resolution implementation of the proteome-wide cellular thermal shift assay (CETSA) to follow protein interaction changes induced by the antimetabolite 5-fluorouracil (5-FU) and related nucleosides. We confirm anticipated effects on the known main target, thymidylate synthase (TYMS), and enzymes in pyrimidine metabolism and DNA damage pathways. However, most interaction changes we see are for proteins previously not associated with the MoA of 5-FU, including wide-ranging effects on RNA-modification and -processing pathways. Attenuated responses of specific proteins in a resistant cell model identify key components of the 5-FU MoA, where intriguingly the abrogation of TYMS inhibition is not required for cell proliferation.
License type:
Publisher Copyright
Funding Info:
This research / project is supported by the his work is also supported by the Singapore’s National Research Foundation (NRF-CRP22-2019-0003) awarded to N.P., P.N.. and L.D. - his work is also supported by the Singapore’s National Research Foundation (NRF-CRP22-2019-0003) awarded to N.P., P.N.. and L.D.
Grant Reference no. : his work is also supported by the Singapore’s National Research Foundation (NRF-CRP22-2019-0003) awarded to N.P., P.N.. and L.D.
Description:
NA
ISSN:
2451-9448
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