Medical Journals

Human Cytomegalovirus-encoded Chemokine Receptor Us28 Promotes Tumorigenesis.

Authors:
  • Maussang David
  • Verzijl Dennis
  • van Walsum Marijke
  • Leurs Rob
  • Holl Jens
  • Pleskoff Olivier
  • Michel Detlef
  • van Dongen Guus A M S
  • Smit Martine J

From: Leiden/Amsterdam Center for Drug Research, Division of Medicinal Chemistry, Faculty of Sciences, Vrije Universiteit, De Boelelaan 1083, 1081 HV, Amsterdam, The Netherlands.

Proceedings of the National Academy of Sciences of the United States of America

  • Publish Date: Aug 2006
  • ISSN: 0027-8424
  • Volume: 103
  • Issue: 35
  • Pages: 13068-73
  • Medium: Print
  • Language: English
  • Citation (JAMA): Maussang David, Verzijl Dennis, van Walsum Marijke, et al. Human Cytomegalovirus-encoded Chemokine Receptor Us28 Promotes Tumorigenesis.. Proc. Natl. Acad. Sci. U.S.A. Aug 2006;103:13068-73

Abstract

Human cytomegalovirus (HCMV) is a widely spread herpesvirus, suggested to play a role in tumor progression. US28, a chemokine receptor encoded by HCMV, binds a broad spectrum of chemokines and constitutively activates various pathways linked to proliferation. Our studies reveal that expression of US28 induces a proangiogenic and transformed phenotype by up-regulating the expression of vascular endothelial growth factor and enhancing cell growth and cell cycle progression. US28-expressing cells promote tumorigenesis when injected into nude mice. The G protein-uncoupled constitutively inactive mutant of US28, induces delayed and attenuated tumor formation, indicating the importance of constitutive receptor activity in the early onset of tumor development. Importantly, also in glioblastoma cells infected with the newly isolated clinical HCMV strain Titan, US28 was shown to be involved in the HCMV-induced angiogenic phenotype. Hence, the constitutively activated chemokine receptor US28 might act as a viral oncogene and enhance and/or promote HCMV-associated tumor progression.

Mesh Headings (Keywords): Animals, COS Cells, Cell Cycle, Cell Transformation, Neoplastic, Cells, Cultured, Cercopithecus aethiops, Cytomegalovirus, Female, Gene Expression, Heterotrimeric GTP-Binding Proteins, Humans, Mice, Mice, Nude, Mitogen-Activated Protein Kinases, NIH 3T3 Cells, Neoplasms, Neovascularization, Pathologic, Phenotype, Promoter Regions (Genetics), Receptors, Chemokine, Vascular Endothelial Growth Factor A, Viral Proteins, p38 Mitogen-Activated Protein Kinases


Check for Full Text / PubMed Unique Identifier (PMID): 16924106


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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