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MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer.
Song, Xiaoyu; Ji, Jiayi; Rothstein, Joseph H; Alexeeff, Stacey E; Sakoda, Lori C; Sistig, Adriana; Achacoso, Ninah; Jorgenson, Eric; Whittemore, Alice S; Klein, Robert J; Habel, Laurel A; Wang, Pei; Sieh, Weiva.
Affiliation
  • Song X; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. xiaoyu.song@mountsinai.org.
  • Ji J; Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA. xiaoyu.song@mountsinai.org.
  • Rothstein JH; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Alexeeff SE; Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Sakoda LC; Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Sistig A; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Achacoso N; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
  • Jorgenson E; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
  • Whittemore AS; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Klein RJ; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
  • Habel LA; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
  • Wang P; Regeneron Genetics Center, Tarrytown, NY, USA.
  • Sieh W; Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, CA, USA.
Nat Commun ; 14(1): 377, 2023 01 23.
Article in En | MEDLINE | ID: mdl-36690614
ABSTRACT
Human bulk tissue samples comprise multiple cell types with diverse roles in disease etiology. Conventional transcriptome-wide association study approaches predict genetically regulated gene expression at the tissue level, without considering cell-type heterogeneity, and test associations of predicted tissue-level expression with disease. Here we develop MiXcan, a cell-type-aware transcriptome-wide association study approach that predicts cell-type-level expression, identifies disease-associated genes via combination of cell-type-level association signals for multiple cell types, and provides insight into the disease-critical cell type. As a proof of concept, we conducted cell-type-aware analyses of breast cancer in 58,648 women and identified 12 transcriptome-wide significant genes using MiXcan compared with only eight genes using conventional approaches. Importantly, MiXcan identified genes with distinct associations in mammary epithelial versus stromal cells, including three new breast cancer susceptibility genes. These findings demonstrate that cell-type-aware transcriptome-wide analyses can reveal new insights into the genetic and cellular etiology of breast cancer and other diseases.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Transcriptome Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2023 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Transcriptome Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2023 Document type: Article Affiliation country: United States