CDC7 inhibition impairs neuroendocrine transformation in lung and prostate tumors through MYC degradation  

作　　者：Alvaro Quintanal-Villalonga Kenta Kawasaki Esther Redin Fathema Uddin Swanand Rakhade Vidushi Durani Amin Sabet Moniquetta Shafer Wouter R.Karthaus Samir Zaidi Yingqian A.Zhan Parvathy Manoj Harsha Sridhar Dennis Kinyua Hong Zhong Barbara P.Mello Metamia Ciampricotti Umesh K.Bhanot Irina Linkov Juan Qiu Radhika A.Patel Colm Morrsey Sanjoy Mehta Jesse Barnes Michael C.Haffner Nichlas D.Socci Richard P.Koche Elisa de Stanchina Sonia Molina-Pinelo Sohrab Salehi Helena A.Yu Joseph M.Chan Charles M.Rudin 

机构地区：[1]Department of Medicine,Thoracic Oncology Service,Memorial Sloan Kettering Cancer Center,New York,NY,USA [2]Cancer Biology and Genetics Program,Sloan Kettering Institute,Memorial Sloan Kettering Cancer Center,New York,NY,USA [3]Vagelos College of Physicians and Surgeons,Columbia University,New York,NY,USA [4]Weill Cornell Graduate School of Medical Sciences,Weill Cornell Medicine,New York,NY,UA [5]Human Oncology and Pathogenesis Program,Memorial Sloan Kettering Cancer Center,New York,NY,USA [6]Center for Epigenetics Research,Memorial Sloan Kettering Cancer Center,New York,NY,USA [7]Pathology Core Facilty,Department of Pathology and Laboratory Medicine,MSKCC,New York,NY,USA [8]Antitumor Assessment Core,Memorial Sloan Kettering Cancer Center,New York,NY,USA [9]Divisionsof Human Biology and Clinical Research,Fred Hutchinon Cancer Center,Seattle,WA,USA [10]Deparmentof Urology,University of Washington,Seattle,WA,USA [11]Gene Editing&Screening Core Facility Memorial Sloan Kettering Cancer Center,New York,NY,USA [12]Department of Laboratory Medicine and Pathology,University of Washington,Seattle,WA,USA [13]Bioinfomatics CoreFacility,Memorial Soan Kettering Cancer Center,New York,NY,USA [14]Institute of Biomedicine of Seille(Bis),HUR,CSC,Universidad de Sevilla,Seville,Spain [15]Computational Oncology,Department of Epidemiology and Biostatistics,Memorial Sloan Kettering Cancer Center,New York,NY,USA [16]Well Cornell Medical College New York,NY,USA [17]Present address:Swiss Institute for Experimental Cancer Research(ISREC),School of Life Sciences,EPFL,Lausanne,Switzerland

出　　处：《Signal Transduction and Targeted Therapy》2024年第8期3519-3532,共14页信号转导与靶向治疗（英文）

基　　金：This study was supported by PO1 NIH PO1CA163227(Prostate Cancer Donor Program),NIH T32 CA1600001(to A.Q.V.),NCI R01 CA264078(to C.M.R.and,H.A.Y.);The Doris Duke Foundation(Grant 2021184)(to MCH),NCI P50 CA97186(to M.H.and C.M.),NCI R35 CA263816(to C.M.R.),NCI U24 CA213274(to C.M.R.),Yasuda Medical Foundation(to K.K.);the American Lung Association(to A.Q.V.);the Druckenmiller Center for Lung Cancer Research(to A.Q.V.,K.K.,and C.M.R.);This study was also supported by the Regional Ministry of Health and Consume of Andalucia RC-0004-2020(SMP);the Carlos II Health Institute through the projects"PI20/01109 and PI23/01679"(Co-funded by European Regional Development Fund/European Social Fund;"A way to make Europe""nvesting in your future")(SMP).

摘　　要：Neuroendocrine(NE)transformation is a mechanism of resistance to targeted therapy in lung and prostate adenocarcinomas leading to poor prognosis.Up to date,even if patients at high risk of transformation can be identified by the occurrence of Tumor Protein P53(TP53)and Retinoblastoma Transcriptional Corepressor 1(RB1)mutations in their tumors,no therapeutic strategies are available to prevent or delay histological transformation.Upregulation of the cell cycle kinase Cell Division Cycle 7(CDC7)occurred in tumors during the initial steps of NE transformation,already after TP53/RB1 co-inactivation,leading to induced sensitivity to the CDC7 inhibitor simurosertib.CDC7 inhibition suppressed NE transdifferentiation and extended response to targeted therapy in in vivo models of NE transformation by inducing the proteasome-mediated degradation of the MYC Proto-Oncogen(MYC),implicated in stemness and histological transformation.Ectopic overexpression of a degradation-resistant MYC isoform reestablished the NE transformation phenotype observed on targeted therapy,even in the presence of simurosertib.CDC7 inhibition also markedly extended response to standard cytotoxics(cisplatin,irinotecan)in lung and prostate small cell carcinoma models.These results nominate CDC7 inhibition as a therapeutic strategy to constrain lineage plasticity,as well as to effectively treat NE tumors de novo or after transformation.As simurosertib clinical efficacy trials are ongoing,this concept could be readily translated for patients at risk oftransformation.

关 键 词：TUMORS markedly TRANSFORMATION 

分 类 号：R737.25[医药卫生—肿瘤]