Journal article

An orally bioavailable Chk1 inhibitor, CCT244747, sensitizes bladder and head and neck cancer cell lines to radiation

R Patel, HE Barker, J Kyula, M McLaughlin, MT Dillon, U Schick, H Hafsi, A Thompson, V Khoo, K Harrington, S Zaidi

Radiotherapy and Oncology | ELSEVIER IRELAND LTD | Published : 2017

Abstract

Purpose Chk1 inhibition increases cell sensitivity to both chemotherapy and radiotherapy in several tumour types and is, therefore, a promising anti-cancer approach. Although several Chk1 inhibitors have been developed, their clinical progress has been hampered by low bioavailability and off-target toxicities. Materials and methods We characterized the radiosensitizing activity of CCT244747, the first orally bioavailable Chk1 inhibitor. We used a panel of bladder and head and neck cancer cell lines and monitored the effect of combining CCT244747 with radiation both in in vitro and in vivo models. Results CCT244747 sensitized cancer cell lines to radiation in vitro and resulted in a growth de..

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University of Melbourne Researchers

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Awarded by CRUK



Funding Acknowledgements

KJH received support from the ICR/RM NIHR Biomedical Research Centre, the Oracle Cancer Trust, The Rosetree Trust and The Anthony Long Trust. KJH, HB, MTD acknowledge research funding from CRUK (C7224/A13407). RP received funding from the Department of Urology, the Royal Marsden Hospital, London and a generous research donation from Lord and Lady Colin Marshall of Knightsbridge. We would like to thank Ian Collins, Michelle Garrett and Tom Matthews for providing CCT244747.