| Literature DB >> 31883968 |
Hua Zhang1, Camilla L Christensen2, Ruben Dries3, Matthew G Oser2, Jiehui Deng4, Brian Diskin5, Fei Li4, Yuanwang Pan4, Xuzhu Zhang6, Yandong Yin6, Eleni Papadopoulos4, Val Pyon4, Cassandra Thakurdin4, Nicholas Kwiatkowski7, Kandarp Jani2, Alexandra R Rabin4, Dayanne M Castro8, Ting Chen4, Heather Silver4, Qingyuan Huang4, Mirna Bulatovic4, Catríona M Dowling4, Belen Sundberg5, Alan Leggett7, Michela Ranieri4, Han Han4, Shuai Li4, Annan Yang2, Kristen E Labbe4, Christina Almonte4, Vladislav O Sviderskiy9, Max Quinn4, Jack Donaghue4, Eric S Wang7, Tinghu Zhang7, Zhixiang He7, Vamsidhar Velcheti4, Peter S Hammerman2, Gordon J Freeman10, Richard Bonneau8, William G Kaelin11, Kate D Sutherland12, Ariena Kersbergen13, Andrew J Aguirre14, Guo-Cheng Yuan3, Eli Rothenberg6, George Miller5, Nathanael S Gray15, Kwok-Kin Wong16.
Abstract
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.Entities:
Keywords: CDK7; YKL-5-124; anti-tumor immunity; cell cycle; genome instability; immune checkpoint blockade; immunotherapy; replication stress; single-cell analysis; small cell lung cancer
Mesh:
Substances:
Year: 2019 PMID: 31883968 PMCID: PMC7277075 DOI: 10.1016/j.ccell.2019.11.003
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743