CX-5461 is a DNA G-quadruplex stabilizer with selective lethality in BRCA1/2 deficient tumours

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作者
Hong Xu
Marco Di Antonio
Steven McKinney
Veena Mathew
Brandon Ho
Nigel J. O’Neil
Nancy Dos Santos
Jennifer Silvester
Vivien Wei
Jessica Garcia
Farhia Kabeer
Daniel Lai
Priscilla Soriano
Judit Banáth
Derek S. Chiu
Damian Yap
Daniel D. Le
Frank B. Ye
Anni Zhang
Kelsie Thu
John Soong
Shu-chuan Lin
Angela Hsin Chin Tsai
Tomo Osako
Teresa Algara
Darren N. Saunders
Jason Wong
Jian Xian
Marcel B. Bally
James D. Brenton
Grant W. Brown
Sohrab P. Shah
David Cescon
Tak W. Mak
Carlos Caldas
Peter C. Stirling
Phil Hieter
Shankar Balasubramanian
Samuel Aparicio
机构
[1] British Columbia Cancer Research Centre,Department of Molecular Oncology, and Department of Pathology and Laboratory Medicine
[2] University of British Columbia,Department of Chemistry
[3] Cancer Research UK Cambridge Research Institute,Department of Biochemistry and Donnelly Centre
[4] Li Ka Shing Centre,BC Cancer Agency and Department of Pathology and Laboratory Medicine
[5] Robinson Way,Department of Integrative Oncology
[6] ,Cancer Research UK Cambridge Research Institute and Department of Oncology
[7] University of Cambridge,Division of Medical Oncology and Hematology, Department of Medicine
[8] Terry Fox Laboratory,undefined
[9] BC Cancer Agency,undefined
[10] University of Toronto,undefined
[11] Michael Smith Laboratories,undefined
[12] University of British Columbia,undefined
[13] Advanced Therapeutics,undefined
[14] University of British Columbia,undefined
[15] Campbell Family Institute for Breast Cancer Research,undefined
[16] Princess Margret Cancer Centre,undefined
[17] BC Cancer Agency,undefined
[18] Senhwa Biosciences,undefined
[19] Inc.,undefined
[20] University of Cambridge,undefined
[21] Li Ka Shing Centre,undefined
[22] University of Toronto,undefined
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摘要
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).
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