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Cancer stem cells from human breast tumors are involved in spontaneous metastases in orthotopic mouse models

机译:人类乳腺肿瘤的癌症干细胞参与原位小鼠模型的自发转移

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摘要

To examine the role of breast cancer stem cells (BCSCs) in metastasis, we generated human-in-mouse breast cancer orthotopic models using patient tumor specimens, labeled with optical reporter fusion genes. These models recapitulate human cancer features not captured with previous models, including spontaneous metastasis in particular, and provide a useful platform for studies of breast tumor initiation and progression. With noninvasive imaging approaches, as few as 10 cells of stably labeled BCSCs could be tracked in vivo, enabling studies of early tumor growth and spontaneous metastasis. These advances in BCSC imaging revealed that CD44+ cells from both primary tumors and lung metastases are highly enriched for tumor-initiating cells. Our metastatic cancer models, combined with noninvasive imaging techniques, constitute an integrated approach that could be applied to dissect the molecular mechanisms underlying the dissemination of metastatic CSCs (MCSCs) and to explore therapeutic strategies targeting MCSCs in general or to evaluate individual patient tumor cells and predict response to therapy.
机译:为了检查乳腺癌干细胞(BCSCs)在转移中的作用,我们使用患者的肿瘤标本生成了人鼠乳腺癌原位模型,并标有光学报告​​基因融合基因。这些模型概括了先前模型未捕获的人类癌症特征,尤其是自发转移,并为研究乳腺癌的发生和发展提供了有用的平台。使用非侵入性成像方法,可以在体内追踪多达10个稳定标记的BCSC细胞,从而能够研究早期肿瘤的生长和自发转移。 BCSC成像的这些进展表明,来自原发性肿瘤和肺转移的CD44 +细胞高度富含肿瘤引发细胞。我们的转移性癌症模型与无创成像技术相结合,构成了一种综合方法,可用于剖析转移性CSCs(MCSCs)传播的分子机制,并探索针对MCSCs的治疗策略,或评估单个患者肿瘤细胞和预测对治疗的反应。

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