Goswami Sumanta, Sahai Erik, Wyckoff Jeffrey B, Cammer Michael, Cox Dianne, Pixley Fiona J, Stanley E Richard, Segall Jeffrey E, Condeelis John S
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Cancer Res. 2005 Jun 15;65(12):5278-83. doi: 10.1158/0008-5472.CAN-04-1853.
Previous studies have shown that macrophages and tumor cells are comigratory in mammary tumors and that these cell types are mutually dependent for invasion. Here we show that macrophages and tumor cells are necessary and sufficient for comigration and invasion into collagen I and that this process involves a paracrine loop. Macrophages express epidermal growth factor (EGF), which promotes the formation of elongated protrusions and cell invasion by carcinoma cells. Colony stimulating factor 1 (CSF-1) produced by carcinoma cells promotes the expression of EGF by macrophages. In addition, EGF promotes the expression of CSF-1 by carcinoma cells thereby generating a positive feedback loop. Disruption of this loop by blockade of either EGF receptor or CSF-1 receptor signaling is sufficient to inhibit both macrophage and tumor cell migration and invasion.
先前的研究表明,巨噬细胞和肿瘤细胞在乳腺肿瘤中共同迁移,并且这些细胞类型在侵袭过程中相互依赖。在此我们表明,巨噬细胞和肿瘤细胞对于共同迁移和侵袭进入I型胶原是必要且充分的,并且这一过程涉及一个旁分泌环。巨噬细胞表达表皮生长因子(EGF),其促进癌细胞形成细长的突起并促进细胞侵袭。癌细胞产生的集落刺激因子1(CSF-1)促进巨噬细胞表达EGF。此外,EGF促进癌细胞表达CSF-1,从而产生一个正反馈环。通过阻断EGF受体或CSF-1受体信号来破坏这个环足以抑制巨噬细胞和肿瘤细胞的迁移与侵袭。