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The impact of bone morphogenetic protein 4 (BMP4) on breast cancer metastasis in a mouse xenograft model

机译:骨形态发生蛋白4(BMP4)对小鼠异种移植模型乳腺癌转移的影响

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Bone morphogenetic protein 4 (BMP4) is a key regulator of cell proliferation and differentiation. In breast cancer cells, BMP4 has been shown to reduce proliferation in vitro and interestingly, in some cases, also to induce migration and invasion. Here we investigated whether BMP4 influences breast cancer metastasis formation by using a xenograft mouse model. MDA-MB-231 breast cancer cells were injected intracardially into mice and metastasis formation was monitored using bioluminescence imaging. Mice treated with BMP4 developed metastases slightly earlier as compared to control animals but the overall number of metastases was similar in both groups (13 in the BMP4 group vs. 12 in controls). In BMP4treated mice, bone metastases were more common (10 vs. 7) but adrenal gland metastases were less frequent (1 vs. 5) than in controls. Immunostaining revealed no differences in signaling activation, proliferation rate, blood vessel formation, EMT markers or the number of cancer -associated fibroblasts between the treatment groups. In conclusion, BMP4 caused a trend towards accelerated metastasis formation, especially in bone. More work is needed to uncover the long-term effects of BMP4 and the clinical relevance of these findings. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:骨形态发生蛋白4(BMP4)是细胞增殖和分化的关键调节剂。在乳腺癌细胞中,已显示BMP4可以在体外减少增殖,有趣的是,在某些情况下,还可以诱导迁移和侵袭。在这里,我们调查了BMP4是否通过使用异种移植小鼠模型影响乳腺癌转移的形成。将MDA-MB-231乳腺癌细胞心内注射到小鼠中,并使用生物发光成像监测转移的形成。与对照动物相比,用BMP4处理的小鼠发生转移的时间稍早,但两组的转移总数相似(BMP4组为13,对照组为12)。在BMP4处理的小鼠中,骨转移更为常见(10比7),但肾上腺转移的频率(1比5)比对照组低。免疫染色显示治疗组之间在信号激活,增殖速率,血管形成,EMT标记或与癌症相关的成纤维细胞数量方面无差异。总之,BMP4导致加速转移形成的趋势,尤其是在骨中。需要更多的工作来揭示BMP4的长期作用以及这些发现的临床意义。 (C)2016 Elsevier Ireland Ltd.保留所有权利。

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