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作者:Ngoepe, Nare
作者单位:University of Copenhagen
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作者:Al Bakir, Maise; Reading, James L.; Gamble, Samuel; Rosenthal, Rachel; Uddin, Imran; Rowan, Andrew; Przewrocka, Joanna; Rogers, Amber; Wong, Yien Ning Sophia; Bentzen, Amalie K.; Veeriah, Selvaraju; Ward, Sophia; Garnett, Aaron T.; Kalavakur, Paula; Martinez-Ruiz, Carlos; Puttick, Clare; Huebner, Ariana; Cook, Daniel E.; Moore, David A.; Abbosh, Chris; Hiley, Crispin T.; Naceur-Lombardelli, Cristina; Watkins, Thomas B. K.; Petkovic, Marina; Schwarz, Roland F.; Galvez-Cancino, Felipe; Litchfield, Kevin; Meldgaard, Peter; Sorensen, Boe Sandahl; Madsen, Line Bille; Jaeger, Dirk; Forster, Martin D.; Arkenau, Tobias; Domingo-Vila, Clara; Tree, Timothy I. M.; Kadivar, Mohammad; Hadrup, Sine Reker; Chain, Benny; Quezada, Sergio A.; McGranahan, Nicholas; Swanton, Charles
作者单位:Francis Crick Institute; Cancer Research UK; University of London; University College London; University of London; University College London; University of London; University College London; Francis Crick Institute; University of London; University College London; University College London Hospitals NHS Foundation Trust; University of London; University College London; Helmholtz Association; Max Delbruck Center for Molecular Medicine; Humboldt University of Berlin; Free University of Berlin; Humboldt University of Berlin; Charite Universitatsmedizin Berlin; Free University of Berlin; Humboldt University of Berlin; University of Cologne; University of Cologne; University of Oxford; Aarhus University; Aarhus University; Aarhus University; Ruprecht Karls University Heidelberg; University of London; University College London; University of London; University College London
摘要:Neoantigen vaccines are under investigation for various cancers, including epidermal growth factor receptor (EGFR)-driven lung cancers1,2. We tracked the phylogenetic history of an EGFR mutant lung cancer treated with erlotinib, osimertinib, radiotherapy and a personalized neopeptide vaccine (NPV) targeting ten somatic mutations, including EGFR exon 19 deletion (ex19del). The ex19del mutation was clonal, but is likely to have appeared after a whole-genome doubling (WGD) event. Following osimer...
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作者:Wiemann, Jasmina
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作者:Barron, Tara; Yalcin, Belgin; Su, Minhui; Byun, Youkyeong Gloria; Gavish, Avishai; Shamardani, Kiarash; Xu, Haojun; Ni, Lijun; Soni, Neeraj; Mehta, Vilina; Maleki Jahan, Samin; Kim, Yoon Seok; Taylor, Kathryn R.; Keough, Michael B.; Quezada, Michael A.; Geraghty, Anna C.; Mancusi, Rebecca; Vo, Linh Thuy; Castaneda, Enrique Herrera; Woo, Pamelyn J.; Petritsch, Claudia K.; Vogel, Hannes; Kaila, Kai; Monje, Michelle
作者单位:Stanford University; Howard Hughes Medical Institute; Stanford University; Stanford University; Stanford University; University of Helsinki; University of Helsinki
摘要:High-grade gliomas (HGGs) are the leading cause of brain cancer-related death. HGGs include clinically, anatomically and molecularly distinct subtypes that stratify into diffuse midline gliomas (DMGs), such as H3K27M-altered diffuse intrinsic pontine glioma, and hemispheric HGGs, such as IDH wild-type glioblastoma. Neuronal activity drives glioma progression through paracrine signalling1,2 and neuron-to-glioma synapses3, 4, 5-6. Glutamatergic AMPA receptor-dependent synapses between neurons an...
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作者:Naddaf, Miryam
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作者:[Anonymous]
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作者:Fleming, Nic
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作者:Kozlov, Max
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作者:Sebastian, Robin; Sun, Eric G.; Fedkenheuer, Michael; Fu, Haiqing; Jung, Seolkyoung; Thakur, Bhushan L.; Redon, Christophe E.; Pegoraro, Gianluca; Tran, Andy D.; Gross, Jacob M.; Mosavarpour, Sara; Kusi, Nana Afua; Ray, Anagh; Dhall, Anjali; Pongor, Lorinc S.; Casellas, Rafael; Aladjem, Mirit I.
作者单位:National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI); National Institutes of Health (NIH) - USA; NIH National Institute of Arthritis & Musculoskeletal & Skin Diseases (NIAMS); National Institutes of Health (NIH) - USA; NIH National Institute of Arthritis & Musculoskeletal & Skin Diseases (NIAMS); National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI); National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI); Cornell University; Weill Cornell Medicine; Rockefeller University; Memorial Sloan Kettering Cancer Center; University of Texas System; UTMD Anderson Cancer Center
摘要:DNA double-strand breaks (DSBs) disrupt the continuity of the genome, with consequences for malignant transformation. Massive DNA damage can elicit a cellular checkpoint response that prevents cell proliferation1,2. However, how highly aggressive cancer cells, which can tolerate widespread DNA damage, respond to DSBs alongside continuous chromosome duplication is unknown. Here we show that DSBs induce a local genome maintenance mechanism that inhibits replication initiation in DSB-containing t...
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作者:[Anonymous]