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Jerantinine A induces tumor-specific cell death through modulation of splicing factor 3b subunit 1 (SF3B1)

Chung, Felicia Fei-Lei; Tan, Perry Faith Tze Ming; Raja, Vijay Joseph; Tan, Boon-Shing; Lim, Kuan-Hon; Kam, Toh-Seok; Hii, Ling-Wei; Tan, Si Hoey; See, Sze-Jia; Tan, Yuen-Fen; Wong, Li-Zhe; Yam, Wai Keat; Mai, Chun Wai; Bradshaw, Tracey D.; Leong, Chee-Onn

Jerantinine A induces tumor-specific cell death through modulation of splicing factor 3b subunit 1 (SF3B1) Thumbnail


Authors

Felicia Fei-Lei Chung

Perry Faith Tze Ming Tan

Vijay Joseph Raja

Boon-Shing Tan

Kuan-Hon Lim

Toh-Seok Kam

Ling-Wei Hii

Si Hoey Tan

Sze-Jia See

Yuen-Fen Tan

Li-Zhe Wong

Wai Keat Yam

Chun Wai Mai

Tracey D. Bradshaw

Chee-Onn Leong



Abstract

Precursor mRNA (pre-mRNA) splicing is catalyzed by a large ribonucleoprotein complex known as the spliceosome. Numerous studies have indicated that aberrant splicing patterns or mutations in spliceosome components, including the splicing factor 3b subunit 1 (SF3B1), are associated with hallmark cancer phenotypes. This has led to the identification and development of small molecules with spliceosome-modulating activity as potential anticancer agents. Jerantinine A (JA) is a novel indole alkaloid which displays potent anti-proliferative activities against human cancer cell lines by inhibiting tubulin polymerization and inducing G2/M cell cycle arrest. Using a combined pooled-genome wide shRNA library screen and global proteomic profiling, we showed that JA targets the spliceosome by up-regulating SF3B1 and SF3B3 protein in breast cancer cells. Notably, JA induced significant tumor-specific cell death and a significant increase in unspliced pre-mRNAs. In contrast, depletion of endogenous SF3B1 abrogated the apoptotic effects, but not the G2/M cell cycle arrest induced by JA. Further analyses showed that JA stabilizes endogenous SF3B1 protein in breast cancer cells and induced dissociation of the protein from the nucleosome complex. Together, these results demonstrate that JA exerts its antitumor activity by targeting SF3B1 and SF3B3 in addition to its reported targeting of tubulin polymerization.

Citation

Chung, F. F.-L., Tan, P. F. T. M., Raja, V. J., Tan, B.-S., Lim, K.-H., Kam, T.-S., Hii, L.-W., Tan, S. H., See, S.-J., Tan, Y.-F., Wong, L.-Z., Yam, W. K., Mai, C. W., Bradshaw, T. D., & Leong, C.-O. (2017). Jerantinine A induces tumor-specific cell death through modulation of splicing factor 3b subunit 1 (SF3B1). Scientific Reports, 7(42504), https://doi.org/10.1038/srep42504

Journal Article Type Article
Acceptance Date Jan 13, 2017
Publication Date Feb 15, 2017
Deposit Date Mar 8, 2017
Publicly Available Date Mar 8, 2017
Journal Scientific Reports
Electronic ISSN 2045-2322
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 7
Issue 42504
DOI https://doi.org/10.1038/srep42504
Public URL https://nottingham-repository.worktribe.com/output/845632
Publisher URL http://www.nature.com/articles/srep42504
Contract Date Mar 8, 2017

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