Human cytomegalovirus-encoded chemokine receptor US28 promotes tumorigenesis
Author(s) -
David Maussang,
Dennis Verzijl,
Marijke van Walsum,
Rob Leurs,
Jens Holl,
Olivier Pleskoff,
Detlef Michel,
Guus A.M.S. van Dongen,
Martine J. Smit
Publication year - 2006
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0604433103
Subject(s) - chemokine receptor , biology , c c chemokine receptor type 6 , ccr1 , cancer research , carcinogenesis , human cytomegalovirus , tumor progression , chemokine receptor ccr5 , viral oncogene , ccl21 , microbiology and biotechnology , chemokine , receptor , immunology , virus , cancer , genetics
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.
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