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SNAIL1 action in tumor cells influences macrophage polarization and metastasis in breast cancer through altered GM-CSF secretion

机译:SNAIL1在肿瘤细胞中的作用通过改变GM-CSF分泌影响乳腺癌的巨噬细胞极化和转移

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The EMT inducer SNAIL1 regulates breast cancer metastasis and its expression in human primary breast tumor predicts for poor outcomes. During tumor progression SNAIL1 has multiple effects in tumor cells that can impact metastasis. An inflammatory tumor microenvironment also impacts metastasis and recently SNAIL1 has been implicated as modulating the secretion of cytokines that can influence the tumor immune infiltrate. Using a spontaneous genetic model of breast cancer metastasis and syngeneic orthotopic transplant experiments we show that the action of SNAIL1 in primary breast tumor cells is required for breast tumor growth and metastasis. It does so, in part, by regulating production of GM-CSF, IL1α, IL-6, and TNFα by breast cancer cells. The SNAIL1-dependent tumor cell secretome modulates the primary tumor-associated macrophage (TAM) polarization. GM-CSF alone modulates TAM polarization and impacts breast cancer metastasis in vivo. This study highlights another role for breast tumor SNAIL1 in cancer progression to metastasis—modulation of the immune microenvironment of primary breast tumors.
机译:EMT诱导剂SNAIL1调节乳腺癌的转移,其在人原发性乳腺癌中的表达预示不良结局。在肿瘤进展期间,SNAIL1在肿瘤细胞中具有多种作用,可影响转移。炎性肿瘤微环境也影响转移,最近,SNAIL1被认为与调节可影响肿瘤免疫浸润的细胞因子分泌有关。使用乳腺癌转移的自发遗传模型和同基因原位移植实验,我们表明SNAIL1在原发性乳腺癌细胞中的作用是乳腺癌生长和转移所必需的。这样做部分是通过调节乳腺癌细胞产生GM-CSF,IL1α,IL-6和TNFα来实现的。 SNAIL1依赖的肿瘤细胞分泌基因组调节原发性肿瘤相关巨噬细胞(TAM)极化。 GM-CSF单独调节TAM极化并影响体内乳腺癌转移。这项研究强调了乳腺肿瘤SNAIL1在癌症进展为转移中的另一作用-调节原发性乳腺肿瘤的免疫微环境。

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