Alternatively activated macrophages/mononuclear phagocytes promote growth and invasion of breast cancer cell line SKBR3.
- Author:
Ju-jiang GUO
1
;
Feng-xi SU
;
He-rui YAO
;
Ji-sheng CHEN
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Breast Neoplasms; metabolism; Cell Line, Tumor; Cell Proliferation; Chemokines, CC; metabolism; Chick Embryo; Coculture Techniques; Humans; Interleukin-4; metabolism; Macrophage Activation; Phagocytes; immunology; Tumor Necrosis Factor-alpha; metabolism
- From: Journal of Southern Medical University 2007;27(4):410-413
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the effect of alternatively activated macrophages /mononuclear phagocytes(MNP) on breast cancer cells and explore the mechanisms for the action of tumor-associated macrophages in breast cancer.
METHODSHuman peripheral blood monocytes were isolated and cultured in vitro and divided into 3 groups, namely classically activated monocytes (CAM) which were induced by lipopolysaccharide, alternatively activated monocytes (AAM) induce by IL-4, and control cells treated with the culture medium only. After cell culture for 48-72 h, the mRNA of tumor necrosis factor-alpha (TNF-alpha), alternative monocytes activation- associated CC-chemokine 1 (AMAC-1), and beta-actin of the 3 groups were extracted for RT-PCR, or the cells were cocultured with breast cancer cell line SKBR3, or seeded in chicken chorioallantoic membrane along with SKBR3.
RESULTSTNF-alpha mRNA was significantly increased in CAM, and AMAC-1 was highly expressed in AAM. The coculture experiments showed that CAM exhibited obvious inhibitory effect on SKBR3 cells after a 3-day culture whereas AAM significantly promoted the growth of SKBR3 cells after a 5-day culture. In chicken on chorioallantoic membrane experiment, the macrophages promoted tumor angiogenesis and AAM showed the most obvious effect.
CONCLUSIONIL-4 induces high expression of AMAC-1, a molecular marker of AAM, in the macrophages, and AAM can promote the growth of SKBR3 cells and tumor angiogenesis.