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Article: CX-5461 is a DNA G-quadruplex stabilizer with selective lethality in BRCA1/2 deficient tumours
Title | CX-5461 is a DNA G-quadruplex stabilizer with selective lethality in BRCA1/2 deficient tumours |
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Authors | Xu, HongDi Antonio, MarcoMcKinney, StevenMathew, VeenaHo, BrandonO'Neil, Nigel J.Santos, Nancy DosSilvester, JenniferWei, VivienGarcia, JessicaKabeer, FarhiaLai, DanielSoriano, PriscillaBanáth, JuditChiu, Derek S.Yap, DamianLe, Daniel D.Ye, Frank B.Zhang, AnniThu, KelsieSoong, JohnLin, Shu ChuanTsai, Angela Hsin ChinOsako, TomoAlgara, TeresaSaunders, Darren N.Wong, JasonXian, JianBally, Marcel B.Brenton, James D.Brown, Grant W.Shah, Sohrab P.Cescon, DavidMak, Tak W.Caldas, CarlosStirling, Peter C.Hieter, PhilBalasubramanian, ShankarAparicio, Samuel |
Issue Date | 2017 |
Citation | Nature Communications, 2017, v. 8, article no. 14432 How to Cite? |
Abstract | G-quadruplex DNAs form four-stranded helical structures and are proposed to play key roles in different cellular processes. Targeting G-quadruplex DNAs for cancer treatment is a very promising prospect. Here, we show that CX-5461 is a G-quadruplex stabilizer, with specific toxicity against BRCA deficiencies in cancer cells and polyclonal patient-derived xenograft models, including tumours resistant to PARP inhibition. Exposure to CX-5461, and its related drug CX-3543, blocks replication forks and induces ssDNA gaps or breaks. The BRCA and NHEJ pathways are required for the repair of CX-5461 and CX-3543-induced DNA damage and failure to do so leads to lethality. These data strengthen the concept of G4 targeting as a therapeutic approach, specifically for targeting HR and NHEJ deficient cancers and other tumours deficient for DNA damage repair. CX-5461 is now in advanced phase I clinical trial for patients with BRCA1/2 deficient tumours (Canadian trial, NCT02719977, opened May 2016). |
Persistent Identifier | http://hdl.handle.net/10722/293001 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Xu, Hong | - |
dc.contributor.author | Di Antonio, Marco | - |
dc.contributor.author | McKinney, Steven | - |
dc.contributor.author | Mathew, Veena | - |
dc.contributor.author | Ho, Brandon | - |
dc.contributor.author | O'Neil, Nigel J. | - |
dc.contributor.author | Santos, Nancy Dos | - |
dc.contributor.author | Silvester, Jennifer | - |
dc.contributor.author | Wei, Vivien | - |
dc.contributor.author | Garcia, Jessica | - |
dc.contributor.author | Kabeer, Farhia | - |
dc.contributor.author | Lai, Daniel | - |
dc.contributor.author | Soriano, Priscilla | - |
dc.contributor.author | Banáth, Judit | - |
dc.contributor.author | Chiu, Derek S. | - |
dc.contributor.author | Yap, Damian | - |
dc.contributor.author | Le, Daniel D. | - |
dc.contributor.author | Ye, Frank B. | - |
dc.contributor.author | Zhang, Anni | - |
dc.contributor.author | Thu, Kelsie | - |
dc.contributor.author | Soong, John | - |
dc.contributor.author | Lin, Shu Chuan | - |
dc.contributor.author | Tsai, Angela Hsin Chin | - |
dc.contributor.author | Osako, Tomo | - |
dc.contributor.author | Algara, Teresa | - |
dc.contributor.author | Saunders, Darren N. | - |
dc.contributor.author | Wong, Jason | - |
dc.contributor.author | Xian, Jian | - |
dc.contributor.author | Bally, Marcel B. | - |
dc.contributor.author | Brenton, James D. | - |
dc.contributor.author | Brown, Grant W. | - |
dc.contributor.author | Shah, Sohrab P. | - |
dc.contributor.author | Cescon, David | - |
dc.contributor.author | Mak, Tak W. | - |
dc.contributor.author | Caldas, Carlos | - |
dc.contributor.author | Stirling, Peter C. | - |
dc.contributor.author | Hieter, Phil | - |
dc.contributor.author | Balasubramanian, Shankar | - |
dc.contributor.author | Aparicio, Samuel | - |
dc.date.accessioned | 2020-11-17T14:57:40Z | - |
dc.date.available | 2020-11-17T14:57:40Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Nature Communications, 2017, v. 8, article no. 14432 | - |
dc.identifier.uri | http://hdl.handle.net/10722/293001 | - |
dc.description.abstract | G-quadruplex DNAs form four-stranded helical structures and are proposed to play key roles in different cellular processes. Targeting G-quadruplex DNAs for cancer treatment is a very promising prospect. Here, we show that CX-5461 is a G-quadruplex stabilizer, with specific toxicity against BRCA deficiencies in cancer cells and polyclonal patient-derived xenograft models, including tumours resistant to PARP inhibition. Exposure to CX-5461, and its related drug CX-3543, blocks replication forks and induces ssDNA gaps or breaks. The BRCA and NHEJ pathways are required for the repair of CX-5461 and CX-3543-induced DNA damage and failure to do so leads to lethality. These data strengthen the concept of G4 targeting as a therapeutic approach, specifically for targeting HR and NHEJ deficient cancers and other tumours deficient for DNA damage repair. CX-5461 is now in advanced phase I clinical trial for patients with BRCA1/2 deficient tumours (Canadian trial, NCT02719977, opened May 2016). | - |
dc.language | eng | - |
dc.relation.ispartof | Nature Communications | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | CX-5461 is a DNA G-quadruplex stabilizer with selective lethality in BRCA1/2 deficient tumours | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1038/ncomms14432 | - |
dc.identifier.pmid | 28211448 | - |
dc.identifier.pmcid | PMC5321743 | - |
dc.identifier.scopus | eid_2-s2.0-85013159255 | - |
dc.identifier.volume | 8 | - |
dc.identifier.spage | article no. 14432 | - |
dc.identifier.epage | article no. 14432 | - |
dc.identifier.eissn | 2041-1723 | - |
dc.identifier.isi | WOS:000394245100001 | - |
dc.identifier.issnl | 2041-1723 | - |