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Spatial domain analysis predicts risk of colorectal cancer recurrence and infers associated tumor microenvironment networks.
Uttam, Shikhar; Stern, Andrew M; Sevinsky, Christopher J; Furman, Samantha; Pullara, Filippo; Spagnolo, Daniel; Nguyen, Luong; Gough, Albert; Ginty, Fiona; Lansing Taylor, D; Chakra Chennubhotla, S.
Afiliação
  • Uttam S; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA. shf28@pitt.edu.
  • Stern AM; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Sevinsky CJ; University of Pittsburgh Drug Discovery Institute, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Furman S; Biology and Applied Physics, GE Global Research Center, Niskayuna, NY, 12309, USA.
  • Pullara F; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Spagnolo D; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Nguyen L; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Gough A; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Ginty F; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Lansing Taylor D; University of Pittsburgh Drug Discovery Institute, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Chakra Chennubhotla S; Biology and Applied Physics, GE Global Research Center, Niskayuna, NY, 12309, USA.
Nat Commun ; 11(1): 3515, 2020 07 14.
Article em En | MEDLINE | ID: mdl-32665557
ABSTRACT
An unmet clinical need in solid tumor cancers is the ability to harness the intrinsic spatial information in primary tumors that can be exploited to optimize prognostics, diagnostics and therapeutic strategies for precision medicine. Here, we develop a transformational spatial analytics computational and systems biology platform (SpAn) that predicts clinical outcomes and captures emergent spatial biology that can potentially inform therapeutic strategies. We apply SpAn to primary tumor tissue samples from a cohort of 432 chemo-naïve colorectal cancer (CRC) patients iteratively labeled with a highly multiplexed (hyperplexed) panel of 55 fluorescently tagged antibodies. We show that SpAn predicts the 5-year risk of CRC recurrence with a mean AUROC of 88.5% (SE of 0.1%), significantly better than current state-of-the-art methods. Additionally, SpAn infers the emergent network biology of tumor microenvironment spatial domains revealing a spatially-mediated role of CRC consensus molecular subtype features with the potential to inform precision medicine.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Recidiva Local de Neoplasia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Recidiva Local de Neoplasia Idioma: En Ano de publicação: 2020 Tipo de documento: Article