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Tumor properties mediate the relationship between peripheral blood monocytes and tumor-associated macrophages in breast cancer M. N. Stakheyeva, M. R. Patysheva, E. V. Kaigorodova [et al.]

Contributor(s): Stakheyeva, Marina N | Patysheva, Marina R | Kaigorodova, Evgeniya V | Zavyalova, Marina V | Tarabanovskaya, Natalia A | Choynzonov, Evgeny L, 1952- | Cherdyntseva, Nadezhda VMaterial type: ArticleArticleContent type: Текст Media type: электронный Subject(s): рак молочной железы | моноциты | опухолеассоциированные макрофаги | циркулирующие опухолевые клеткиGenre/Form: статьи в журналах Online resources: Click here to access online In: Cancer investigation Vol. 40, № 5. P. 442-456Abstract: In cancer patients, circulating monocytes show functional alterations. Since monocytes are precursors of tumor-associated macrophages (TAMs), TAMs ensuring tumor viability are potentially replenished through the recruitment of monocytes with specific properties. We demonstrated that locoregional metastasis and circulating factors, such as CD45-EpCAM + CD44 + CD24-/low circulating tumor cells, and serum MCP-1 and HMGB1 were statistically associated with modulation of the monocyte features in breast cancer patients. The count of circulating CD45-EpCAM + cells correlated with CD68+, CD163 + monocyte in blood, and with density of CD68 + TAM in breast cancer tumors. Overall, the relationship between monocytes and TAMs is mediated by the tumor in breast cancer patients.
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In cancer patients, circulating monocytes show functional alterations. Since monocytes are precursors of tumor-associated macrophages (TAMs), TAMs ensuring tumor viability are potentially replenished through the recruitment of monocytes with specific properties. We demonstrated that locoregional metastasis and circulating factors, such as CD45-EpCAM + CD44 + CD24-/low circulating tumor cells, and serum MCP-1 and HMGB1 were statistically associated with modulation of the monocyte features in breast cancer patients. The count of circulating CD45-EpCAM + cells correlated with CD68+, CD163 + monocyte in blood, and with density of CD68 + TAM in breast cancer tumors. Overall, the relationship between monocytes and TAMs is mediated by the tumor in breast cancer patients.

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