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Imaging-AMARETTO: An Imaging Genomics Software Tool to Interrogate Multiomics Networks for Relevance to Radiography and Histopathology Imaging Biomarkers of Clinical Outcomes.
Gevaert, Olivier; Nabian, Mohsen; Bakr, Shaimaa; Everaert, Celine; Shinde, Jayendra; Manukyan, Artur; Liefeld, Ted; Tabor, Thorin; Xu, Jishu; Lupberger, Joachim; Haas, Brian J; Baumert, Thomas F; Hernaez, Mikel; Reich, Michael; Quintana, Francisco J; Uhlmann, Erik J; Krichevsky, Anna M; Mesirov, Jill P; Carey, Vincent; Pochet, Nathalie.
Afiliação
  • Gevaert O; Stanford Center for Biomedical Informatics Research, Department of Medicine and Biomedical Data Science, Stanford University, Stanford, CA.
  • Nabian M; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Bakr S; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Everaert C; Ann Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
  • Shinde J; Stanford Center for Biomedical Informatics Research, Department of Medicine and Biomedical Data Science, Stanford University, Stanford, CA.
  • Manukyan A; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Liefeld T; Ann Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
  • Tabor T; Stanford Center for Biomedical Informatics Research, Department of Medicine and Biomedical Data Science, Stanford University, Stanford, CA.
  • Xu J; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Lupberger J; Ann Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
  • Haas BJ; Department of Medicine, University of California, San Diego, San Diego, CA.
  • Baumert TF; Department of Medicine, University of California, San Diego, San Diego, CA.
  • Hernaez M; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Reich M; Rush University Medical Center, Chicago, IL.
  • Quintana FJ; INSERM, U1110, Institut de Recherche sur les Maladies Virales et Hépatiques, Université de Strasbourg, Institut Hopitalo-Universitaire, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Uhlmann EJ; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Krichevsky AM; INSERM, U1110, Institut de Recherche sur les Maladies Virales et Hépatiques, Université de Strasbourg, Institut Hopitalo-Universitaire, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Mesirov JP; Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Champaign, IL.
  • Carey V; Department of Medicine, University of California, San Diego, San Diego, CA.
  • Pochet N; Cell Circuits Program, Broad Institute of MIT and Harvard, Cambridge, MA.
JCO Clin Cancer Inform ; 4: 421-435, 2020 05.
Article em En | MEDLINE | ID: mdl-32383980
ABSTRACT

PURPOSE:

The availability of increasing volumes of multiomics, imaging, and clinical data in complex diseases such as cancer opens opportunities for the formulation and development of computational imaging genomics methods that can link multiomics, imaging, and clinical data.

METHODS:

Here, we present the Imaging-AMARETTO algorithms and software tools to systematically interrogate regulatory networks derived from multiomics data within and across related patient studies for their relevance to radiography and histopathology imaging features predicting clinical outcomes.

RESULTS:

To demonstrate its utility, we applied Imaging-AMARETTO to integrate three patient studies of brain tumors, specifically, multiomics with radiography imaging data from The Cancer Genome Atlas (TCGA) glioblastoma multiforme (GBM) and low-grade glioma (LGG) cohorts and transcriptomics with histopathology imaging data from the Ivy Glioblastoma Atlas Project (IvyGAP) GBM cohort. Our results show that Imaging-AMARETTO recapitulates known key drivers of tumor-associated microglia and macrophage mechanisms, mediated by STAT3, AHR, and CCR2, and neurodevelopmental and stemness mechanisms, mediated by OLIG2. Imaging-AMARETTO provides interpretation of their underlying molecular mechanisms in light of imaging biomarkers of clinical outcomes and uncovers novel master drivers, THBS1 and MAP2, that establish relationships across these distinct mechanisms.

CONCLUSION:

Our network-based imaging genomics tools serve as hypothesis generators that facilitate the interrogation of known and uncovering of novel hypotheses for follow-up with experimental validation studies. We anticipate that our Imaging-AMARETTO imaging genomics tools will be useful to the community of biomedical researchers for applications to similar studies of cancer and other complex diseases with available multiomics, imaging, and clinical data.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma / Genômica por Imageamento Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma / Genômica por Imageamento Idioma: En Ano de publicação: 2020 Tipo de documento: Article