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Merck

CDK7 Inhibition Potentiates Genome Instability Triggering Anti-tumor Immunity in Small Cell Lung Cancer.

Cancer cell (2019-12-31)
Hua Zhang, Camilla L Christensen, Ruben Dries, Matthew G Oser, Jiehui Deng, Brian Diskin, Fei Li, Yuanwang Pan, Xuzhu Zhang, Yandong Yin, Eleni Papadopoulos, Val Pyon, Cassandra Thakurdin, Nicholas Kwiatkowski, Kandarp Jani, Alexandra R Rabin, Dayanne M Castro, Ting Chen, Heather Silver, Qingyuan Huang, Mirna Bulatovic, Catríona M Dowling, Belen Sundberg, Alan Leggett, Michela Ranieri, Han Han, Shuai Li, Annan Yang, Kristen E Labbe, Christina Almonte, Vladislav O Sviderskiy, Max Quinn, Jack Donaghue, Eric S Wang, Tinghu Zhang, Zhixiang He, Vamsidhar Velcheti, Peter S Hammerman, Gordon J Freeman, Richard Bonneau, William G Kaelin, Kate D Sutherland, Ariena Kersbergen, Andrew J Aguirre, Guo-Cheng Yuan, Eli Rothenberg, George Miller, Nathanael S Gray, Kwok-Kin Wong
RÉSUMÉ

Cyclin-dependent kinase 7 (CDK7) is a central regulator of the cell cycle and gene transcription. However, little is known about its impact on genomic instability and cancer immunity. Using a selective CDK7 inhibitor, YKL-5-124, we demonstrated that CDK7 inhibition predominately disrupts cell-cycle progression and induces DNA replication stress and genome instability in small cell lung cancer (SCLC) while simultaneously triggering immune-response signaling. These tumor-intrinsic events provoke a robust immune surveillance program elicited by T cells, which is further enhanced by the addition of immune-checkpoint blockade. Combining YKL-5-124 with anti-PD-1 offers significant survival benefit in multiple highly aggressive murine models of SCLC, providing a rationale for new combination regimens consisting of CDK7 inhibitors and immunotherapies.

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