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- Publisher Website: 10.1016/j.ccr.2014.05.006
- Scopus: eid_2-s2.0-84905709109
- PMID: 25043604
- WOS: WOS:000340343800006
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Article: Functional characterization of CFI-400945, a polo-like kinase 4 inhibitor, as a potential anticancer agent
Title | Functional characterization of CFI-400945, a polo-like kinase 4 inhibitor, as a potential anticancer agent |
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Authors | |
Issue Date | 2014 |
Citation | Cancer Cell, 2014, v. 26, n. 2, p. 163-176 How to Cite? |
Abstract | PLK4 was identified as a promising therapeutic target through a systematic approach that combined RNAi screening with gene expression analysis in human breast cancers and cell lines. A drug discovery program culminated in CFI-400945, a potent and selective PLK4 inhibitor. Cancer cells treated with CFI-400945 exhibit effects consistent with PLK4 kinase inhibition, including dysregulated centriole duplication, mitotic defects, and cell death. Oral administration of CFI-400945 to mice bearing human cancer xenografts results in the significant inhibition of tumor growth at doses that are well tolerated. Increased antitumor activity invivo was observed in PTEN-deficient compared to PTEN wild-type cancer xenografts. Our findings provide a rationale for the clinical evaluation of CFI-400945 in patients with solid tumors, in particular those deficient in PTEN. © 2014 Elsevier Inc. |
Persistent Identifier | http://hdl.handle.net/10722/292840 |
ISSN | 2023 Impact Factor: 48.8 2023 SCImago Journal Rankings: 17.507 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Mason, Jacqueline M. | - |
dc.contributor.author | Lin, Dan Chi Chia | - |
dc.contributor.author | Wei, Xin | - |
dc.contributor.author | Che, Yi | - |
dc.contributor.author | Yao, Yi | - |
dc.contributor.author | Kiarash, Reza | - |
dc.contributor.author | Cescon, David W. | - |
dc.contributor.author | Fletcher, Graham C. | - |
dc.contributor.author | Awrey, Donald E. | - |
dc.contributor.author | Bray, Mark R. | - |
dc.contributor.author | Pan, Guohua | - |
dc.contributor.author | Mak, Tak W. | - |
dc.date.accessioned | 2020-11-17T14:57:19Z | - |
dc.date.available | 2020-11-17T14:57:19Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Cancer Cell, 2014, v. 26, n. 2, p. 163-176 | - |
dc.identifier.issn | 1535-6108 | - |
dc.identifier.uri | http://hdl.handle.net/10722/292840 | - |
dc.description.abstract | PLK4 was identified as a promising therapeutic target through a systematic approach that combined RNAi screening with gene expression analysis in human breast cancers and cell lines. A drug discovery program culminated in CFI-400945, a potent and selective PLK4 inhibitor. Cancer cells treated with CFI-400945 exhibit effects consistent with PLK4 kinase inhibition, including dysregulated centriole duplication, mitotic defects, and cell death. Oral administration of CFI-400945 to mice bearing human cancer xenografts results in the significant inhibition of tumor growth at doses that are well tolerated. Increased antitumor activity invivo was observed in PTEN-deficient compared to PTEN wild-type cancer xenografts. Our findings provide a rationale for the clinical evaluation of CFI-400945 in patients with solid tumors, in particular those deficient in PTEN. © 2014 Elsevier Inc. | - |
dc.language | eng | - |
dc.relation.ispartof | Cancer Cell | - |
dc.title | Functional characterization of CFI-400945, a polo-like kinase 4 inhibitor, as a potential anticancer agent | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1016/j.ccr.2014.05.006 | - |
dc.identifier.pmid | 25043604 | - |
dc.identifier.scopus | eid_2-s2.0-84905709109 | - |
dc.identifier.volume | 26 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 163 | - |
dc.identifier.epage | 176 | - |
dc.identifier.eissn | 1878-3686 | - |
dc.identifier.isi | WOS:000340343800006 | - |
dc.identifier.issnl | 1535-6108 | - |