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Hard wiring of normal tissue-specific chromosome-wide gene expression levels is an additional factor driving cancer type-specific aneuploidies.
Patkar, Sushant; Heselmeyer-Haddad, Kerstin; Auslander, Noam; Hirsch, Daniela; Camps, Jordi; Bronder, Daniel; Brown, Markus; Chen, Wei-Dong; Lokanga, Rachel; Wangsa, Darawalee; Wangsa, Danny; Hu, Yue; Lischka, Annette; Braun, Rüdiger; Emons, Georg; Ghadimi, B Michael; Gaedcke, Jochen; Grade, Marian; Montagna, Cristina; Lazebnik, Yuri; Difilippantonio, Michael J; Habermann, Jens K; Auer, Gert; Ruppin, Eytan; Ried, Thomas.
Affiliation
  • Patkar S; Cancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Heselmeyer-Haddad K; Department of Computer Science, University of Maryland, College Park, USA.
  • Auslander N; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Hirsch D; Department of Computer Science, University of Maryland, College Park, USA.
  • Camps J; National Center for Biotechnology Information, NIH, Bethesda, MD, 20892, USA.
  • Bronder D; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Brown M; Gastrointestinal and Pancreatic Oncology Team, Institut D'Investigacions Biomèdiques August Pi i Sunyer, (IDIBAPS), Hospital Clínic of Barcelona, CIBEREHD, 08036, Barcelona, Spain.
  • Chen WD; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Lokanga R; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Wangsa D; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Wangsa D; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Hu Y; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Lischka A; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Braun R; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Emons G; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Ghadimi BM; Section for Translational Surgical Oncology and Biobanking, Department of Surgery, University Medical Center Schleswig Holstein, Campus Lübeck, Lübeck, Germany.
  • Gaedcke J; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Grade M; Section for Translational Surgical Oncology and Biobanking, Department of Surgery, University Medical Center Schleswig Holstein, Campus Lübeck, Lübeck, Germany.
  • Montagna C; Section of Cancer Genomics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
  • Lazebnik Y; Department of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
  • Difilippantonio MJ; Department of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
  • Habermann JK; Department of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
  • Auer G; Department of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
  • Ruppin E; Department of Genetics and Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Ried T; Lerna Consulting, LLC, New Haven, CT, 06511, USA.
Genome Med ; 13(1): 93, 2021 05 25.
Article in En | MEDLINE | ID: mdl-34034815
ABSTRACT

BACKGROUND:

Many carcinomas have recurrent chromosomal aneuploidies specific to the tissue of tumor origin. The reason for this specificity is not completely understood.

METHODS:

In this study, we looked at the frequency of chromosomal arm gains and losses in different cancer types from the The Cancer Genome Atlas (TCGA) and compared them to the mean gene expression of each chromosome arm in corresponding normal tissues of origin from the Genotype-Tissue Expression (GTEx) database, in addition to the distribution of tissue-specific oncogenes and tumor suppressors on different chromosome arms.

RESULTS:

This analysis revealed a complex picture of factors driving tumor karyotype evolution in which some recurrent chromosomal copy number reflect the chromosome arm-wide gene expression levels of the their normal tissue of tumor origin.

CONCLUSIONS:

We conclude that the cancer type-specific distribution of chromosomal arm gains and losses is potentially "hardwiring" gene expression levels characteristic of the normal tissue of tumor origin, in addition to broadly modulating the expression of tissue-specific tumor driver genes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Gene Expression Regulation, Neoplastic / Chromosome Mapping / Aneuploidy / Neoplasms Limits: Humans Language: En Journal: Genome Med Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Gene Expression Regulation, Neoplastic / Chromosome Mapping / Aneuploidy / Neoplasms Limits: Humans Language: En Journal: Genome Med Year: 2021 Document type: Article Affiliation country: United States