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Verfasst von:Holowatyj, Andreana N. [VerfasserIn]   i
 Haffa, Mariam [VerfasserIn]   i
 Lin, Tengda [VerfasserIn]   i
 Scherer, Dominique [VerfasserIn]   i
 Gigić, Biljana [VerfasserIn]   i
 Ose, Jennifer [VerfasserIn]   i
 Warby, Christy A. [VerfasserIn]   i
 Himbert, Caroline [VerfasserIn]   i
 Abbenhardt-Martin, Clare [VerfasserIn]   i
 Achaintre, David [VerfasserIn]   i
 Boehm, Juergen [VerfasserIn]   i
 Boucher, Kenneth M. [VerfasserIn]   i
 Gicquiau, Audrey [VerfasserIn]   i
 Gsur, Andrea [VerfasserIn]   i
 Habermann, Nina [VerfasserIn]   i
 Herpel, Esther [VerfasserIn]   i
 Kauczor, Hans-Ulrich [VerfasserIn]   i
 Keski-Rahkonen, Pekka [VerfasserIn]   i
 Kloor, Matthias [VerfasserIn]   i
 Knebel Doeberitz, Magnus von [VerfasserIn]   i
 Kok, Dieuwertje E. [VerfasserIn]   i
 Nattenmüller, Johanna [VerfasserIn]   i
 Schirmacher, Peter [VerfasserIn]   i
 Schneider, Martin [VerfasserIn]   i
 Schrotz-King, Petra [VerfasserIn]   i
 Simon, Thomas [VerfasserIn]   i
 Ueland, Per M. [VerfasserIn]   i
 Viskochil, Richard [VerfasserIn]   i
 Weijenberg, Matty P. [VerfasserIn]   i
 Scalbert, Augustin [VerfasserIn]   i
 Ulrich, Alexis [VerfasserIn]   i
 Bowers, Laura W. [VerfasserIn]   i
 Hursting, Stephen D. [VerfasserIn]   i
 Ulrich, Cornelia M. [VerfasserIn]   i
Titel:Multi-omics analysis reveals adipose-tumor crosstalk in patients with colorectal cancer
Verf.angabe:Andreana N. Holowatyj, Mariam Haffa, Tengda Lin, Dominique Scherer, Biljana Gigic, Jennifer Ose, Christy A. Warby, Caroline Himbert, Clare Abbenhardt-Martin, David Achaintre, Juergen Boehm, Kenneth M. Boucher, Audrey Gicquiau, Andrea Gsur, Nina Habermann, Esther Herpel, Hans-Ulrich Kauczor, Pekka Keski-Rahkonen, Matthias Kloor, Magnus von Knebel-Doeberitz, Dieuwertje E. Kok, Johanna Nattenmüller, Peter Schirmacher, Martin Schneider, Petra Schrotz-King, Thomas Simon, Per M. Ueland, Richard Viskochil, Matty P. Weijenberg, Augustin Scalbert, Alexis Ulrich, Laura W. Bowers, Stephen D. Hursting, and Cornelia M. Ulrich
E-Jahr:2020
Jahr:July 12, 2020
Umfang:12 S.
Fussnoten:Gesehen am 13.11.2020
Titel Quelle:Enthalten in: Cancer Prevention Research
Ort Quelle:Philadelphia, Pa. : AACR, 2008
Jahr Quelle:2020
Band/Heft Quelle:13(2020), 10, Seite 817-828
ISSN Quelle:1940-6215
Abstract:Obesity and obesity-driven cancer rates are continuing to rise worldwide. We hypothesize that adipocyte-colonocyte interactions are a key driver of obesity-associated cancers. To understand the clinical relevance of visceral adipose tissue in advancing tumor growth, we analyzed paired tumor-adjacent visceral adipose, normal mucosa, and colorectal tumor tissues as well as presurgery blood samples from patients with sporadic colorectal cancer. We report that high peroxisome proliferator-activated receptor gamma (PPARG) visceral adipose tissue expression is associated with glycoprotein VI (GPVI) signaling—the major signaling receptor for collagen—as well as fibrosis and adipogenesis pathway signaling in colorectal tumors. These associations were supported by correlations between PPARG visceral adipose tissue expression and circulating levels of plasma 4-hydroxyproline and serum intercellular adhesion molecule 1 (ICAM1), as well as gene set enrichment analysis and joint gene-metabolite pathway results integration that yielded significant enrichment of genes defining epithelial-to-mesenchymal transition—as in fibrosis and metastasis—and genes involved in glycolytic metabolism, confirmed this association. We also reveal that elevated prostaglandin-endoperoxide synthase 2 (PTGS2) colorectal tumor expression is associated with a fibrotic signature in adipose-tumor crosstalk via GPVI signaling and dendritic cell maturation in visceral adipose tissue. Systemic metabolite and biomarker profiling confirmed that high PTGS2 expression in colorectal tumors is significantly associated with higher concentrations of serum amyloid A and glycine, and lower concentrations of sphingomyelin, in patients with colorectal cancer. This multi-omics study suggests that adipose-tumor crosstalk in patients with colorectal cancer is a critical microenvironment interaction that could be therapeutically targeted. - See related spotlight by Colacino et al., p. 803
DOI:doi:10.1158/1940-6207.CAPR-19-0538
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1158/1940-6207.CAPR-19-0538
 Volltext: https://cancerpreventionresearch.aacrjournals.org/content/13/10/817
 DOI: https://doi.org/10.1158/1940-6207.CAPR-19-0538
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1738663167
Verknüpfungen:→ Zeitschrift

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