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Leptin promotes bone metastasis of breast cancer by activating the SDF-1/CXCR4 axis

机译:瘦素通过激活SDF-1 / CXCR4轴来促进乳腺癌的骨转移

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摘要

Obesity is associated with an increased risk of tumorigenesis, and increased leptin levels can promote tumor metastasis. However, the effects of leptin on bone metastasis in breast cancer are not fully understood. Here, we examined leptin receptor expression and bone metastasis in tissue samples from 96 breast cancer patients. In addition, we investigated the effects of leptin on the metastatic capacity of breast cancer cells using a transwell assays. The results indicated that higher leptin receptor levels in breast cancer cells are associated with increased incidence of bone metastasis in breast cancer patients. Additionally, leptin promoted migration and invasion of breast cancer cells. The SDF-1/CXCR4 axis activated by leptin also promoted bone metastasis of breast cancer. Finally, increased CXCR4 expression was accompanied by high leptin receptor expression in bone metastatic tissues from breast cancer patients. These results indicate that leptin induces bone metastasis of breast cancer by activating the SDF-1/CXCR4 axis.
机译:肥胖与肿瘤发生的风险增加有关,并且增加的瘦素水平可以促进肿瘤转移。然而,瘦素对乳腺癌骨转移的影响尚不完全理解。在这里,我们检查了96例乳腺癌患者组织样本中的瘦素受体表达和骨转移。此外,我们研究了Leptin对乳腺癌细胞转移能力的影响 使用Transwell测定。结果表明,乳腺癌细胞中较高的瘦素受体水平与乳腺癌患者的骨转移发病率增加有关。另外,瘦素促进了乳腺癌细胞的迁移和侵袭。由瘦素激活的SDF-1 / CXCR4轴也促进了乳腺癌的骨转移。最后,增加的CXCR4表达伴随着来自乳腺癌患者的骨转移组织中的高瘦素受体表达。这些结果表明,瘦素通过激活SDF-1 / CXCR4轴来诱导乳腺癌的骨转移。

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