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Stat3 orchestrates interaction between endothelial and tumor cells and inhibition of Stat3 suppresses brain metastasis of breast cancer cells

机译:Stat3协调内皮细胞与肿瘤细胞之间的相互作用抑制Stat3可抑制乳腺癌细胞的脑转移

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摘要

Brain metastasis is a major cause of morbidity and mortality in patients with breast cancer. Our previous studies indicated that Stat3 plays an important role in brain metastasis. Here, we present evidence that Stat3 functions at the level of the microenvironment of brain metastases. Stat3 controlled constitutive and inducible VEGFR2 expression in tumor-associated brain endothelial cells. Furthermore, inhibition of Stat3 by WP1066 decreased the incidence of brain metastases and increased survival in a preclinical model of breast cancer brain metastasis. WP1066 inhibited Stat3 activation in tumor-associated endothelial cells, reducing their infiltration and angiogenesis. WP1066 also inhibited breast cancer cell invasion. Our results indicate that WP1066 can inhibit tumor angiogenesis and brain metastasis mediated by Stat3 in endothelial and tumor cells.
机译:脑转移是乳腺癌患者发病和死亡的主要原因。我们以前的研究表明,Stat3在脑转移中起重要作用。在这里,我们提供证据表明Stat3在脑转移微环境的水平上起作用。 Stat3控制与肿瘤相关的脑内皮细胞中的组成型和诱导型VEGFR2表达。此外,在乳腺癌脑转移的临床前模型中,WP1066对Stat3的抑制作用降低了脑转移的发生率并提高了生存率。 WP1066抑制肿瘤相关内皮细胞中的Stat3活化,减少其浸润和血管生成。 WP1066还抑制乳腺癌细胞的侵袭。我们的结果表明,WP1066可以抑制Stat3介导的内皮细胞和肿瘤细胞中的肿瘤血管生成和脑转移。

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