| Literature DB >> 26998099 |
Takanobu Motoshima1, Yoshihiro Komohara2, Hasita Horlad2, Hirotake Tsukamoto3, Mitsugu Fujita4, Yoichi Saito2, Kenichiro Tanoue5, Yutaka Kasejima5, Yutaka Sugiyama5, Yoshiaki Kawano5, Yasuharu Nishimura3, Motohiro Takeya2, Masatoshi Eto5.
Abstract
Circulating cluster of differentiation (CD)14+ human leukocyte antigen (HLA)-DRlow/- monocytes, those with a lower HLA-DR expression or are negative for HLA-DR, are considered to be involved in systemic immunosuppression in patients with several malignant tumors. However, few studies have investigated in detail the gene expression profile of CD14+HLA-DRlow/- monocytes. In the present study, the mRNA expression levels of immune-associated molecules in CD14+ monocytes isolated from healthy donors and patients with renal cell carcinoma (RCC) were analyzed. Consistent with previous studies, the percentage of HLA-DRlow/- cells in CD14+ monocytes was significantly increased in patients with RCC compared with healthy donors. In 3 of the 4 patients who underwent surgical resection of the primary tumor, the percentage of CD14+HLA-DRlow/- cells was significantly decreased following surgery. The mRNA expression levels of cyclooxygenase 2, transforming growth factor β, interleukin 6R, chemokine (C-C motif) ligand 2 (CCL2), chemokine (C-X-C motif) ligand 10 (CXCL10), oncostatin M, and vascular endothelial growth factor-A in CD14+ monocytes were quantified using reverse transcription-quantitative polymerase chain reaction. The results of the present study revealed that increased expression levels of CCL2 and CXCL10 were inversely correlated with the percentage of CD14+HLA-DRlow/- monocytes. This suggested that monocytes in RCC patients were immunologically suppressed, and that immunosuppression in RCC patients may be due, in part, to the dysfunction of circulating monocytes.Entities:
Keywords: chemokine (C-C motif) ligand 2; chemokine (C-X-C motif) ligand 10; cluster of differentiation 14; myeloid-derived suppressor cells; renal cell carcinoma
Year: 2016 PMID: 26998099 PMCID: PMC4774459 DOI: 10.3892/ol.2016.4132
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967