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Cyclooxygenase-2 in tumor-associated macrophages promotes breast cancer cell survival by triggering a positive-feedback loop between macrophages and cancer cells

机译:肿瘤相关巨噬细胞中的环氧合酶2通过触发巨噬细胞与癌细胞之间的正反馈回路来促进乳腺癌细胞的存活

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摘要

Tumor-associated macrophages (TAMs) play an important role in cancer cell survival, however, the mechanism of which remains elusive. In this study, we found that COX-2 was abundantly expressed in breast TAMs, which was correlated to poor prognosis in breast cancer patients. Ectopic over-expression of COX-2 in TAMs enhanced breast cancer cell survival both in vitro and in vivo. COX-2 in TAMs was determined to be essential for the induction and maintenance of M2-phenotype macrophage polarity. COX-2+ TAMs promoted breast cancer cell proliferation and survival by increasing Bcl-2 and P-gp and decreasing Bax in cancer cells. Furthermore, COX-2 in TAMs induced the expression of COX-2 in breast cancer cells, which in turn promoted M2 macrophage polarization. Inhibiting PI3K/Akt pathway in cancer cells suppressed COX-2+ TAMs-induced cancer cell survival. These findings suggest that COX-2, functions as a key cancer promoting factor by triggering a positive-feedback loop between macrophages and cancer cells, which could be exploited for breast cancer prevention and therapy.
机译:肿瘤相关的巨噬细胞(TAM)在癌细胞的存活中起着重要的作用,但是其机制仍然难以捉摸。在这项研究中,我们发现COX-2在乳腺癌TAM中大量表达,这与乳腺癌患者的不良预后相关。 TAM中异位过量表达COX-2可提高体内和体外乳腺癌细胞的存活率。已确定TAM中的COX-2对于诱导和维持M2表型巨噬细胞极性至关重要。 COX-2 + TAM通过增加癌细胞中的Bcl-2和P-gp并降低Bax来促进乳腺癌细胞的增殖和存活。此外,TAM中的COX-2诱导乳腺癌细胞中COX-2的表达,进而促进M2巨噬细胞极化。抑制癌细胞中的PI3K / Akt通路可抑制COX-2 + TAMs诱导的癌细胞存活。这些发现表明,COX-2通过触发巨噬细胞和癌细胞之间的正反馈回路而起着关键的癌症促进因子的作用,可将其用于乳腺癌的预防和治疗。

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