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Pan-cancer analysis identifies tumor-specific antigens derived from transposable elements.
Shah, Nakul M; Jang, H Josh; Liang, Yonghao; Maeng, Ju Heon; Tzeng, Shin-Cheng; Wu, Angela; Basri, Noah L; Qu, Xuan; Fan, Changxu; Li, Amy; Katz, Benjamin; Li, Daofeng; Xing, Xiaoyun; Evans, Bradley S; Wang, Ting.
Afiliação
  • Shah NM; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Jang HJ; The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
  • Liang Y; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Maeng JH; The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
  • Tzeng SC; Department of Epigenetics, Van Andel Institute, Grand Rapids, MI, USA.
  • Wu A; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Basri NL; The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
  • Qu X; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Fan C; The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
  • Li A; Donald Danforth Plant Science Center, St. Louis, MO, USA.
  • Katz B; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Li D; The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
  • Xing X; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Evans BS; The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
  • Wang T; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
Nat Genet ; 55(4): 631-639, 2023 04.
Article em En | MEDLINE | ID: mdl-36973455
ABSTRACT
Cryptic promoters within transposable elements (TEs) can be transcriptionally reactivated in tumors to create new TE-chimeric transcripts, which can produce immunogenic antigens. We performed a comprehensive screen for these TE exaptation events in 33 TCGA tumor types, 30 GTEx adult tissues and 675 cancer cell lines, and identified 1,068 TE-exapted candidates with the potential to generate shared tumor-specific TE-chimeric antigens (TS-TEAs). Whole-lysate and HLA-pulldown mass spectrometry data confirmed that TS-TEAs are presented on the surface of cancer cells. In addition, we highlight tumor-specific membrane proteins transcribed from TE promoters that constitute aberrant epitopes on the extracellular surface of cancer cells. Altogether, we showcase the high pan-cancer prevalence of TS-TEAs and atypical membrane proteins that could potentially be therapeutically exploited and targeted.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos de DNA Transponíveis / Neoplasias Tipo de estudo: Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Nat Genet Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos de DNA Transponíveis / Neoplasias Tipo de estudo: Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Nat Genet Ano de publicação: 2023 Tipo de documento: Article