癌细胞侵袭的细胞和分子机制。

O De Wever, L Lapeire, A De Boeck, A Hendrix
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引用次数: 0

摘要

恶性肿瘤的特点是癌细胞侵入局部和远处的生态系统。我们的实验室数据回顾,重点是癌细胞和宿主细胞,如肌成纤维细胞,间充质干细胞和脂肪细胞之间的交叉信号。侵袭相关的细胞活动,即上皮到间质转化、同型和异型细胞-细胞粘附、细胞-基质粘附、迁移、蛋白水解和囊泡胞外,依赖于信号转导途径的分支网络,包括三聚体G蛋白、磷酸肌醇3-激酶、src、信号转导和转录激活因子以及小gtp酶的Rab、Rac和Rho家族的激活。蛋白水解在入侵中的作用不仅限于细胞外基质的分解,而且还导致细胞表面糖蛋白的促血管生成片段的分裂。一些参与侵袭相关活动的细胞类型或分子可以作为预后生物标志物或患者定制治疗的靶点。
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Cellular and molecular mechanisms of cancer cell invasion.

Cancer malignancy is characterized by cancer cell invasion within local and distant ecosystems. Data from our laboratory are reviewed with a focus on cross-signaling between cancer cells and host cells such as myofibroblasts, mesenchymal stem cells and adipocytes. Invasion-associated cellular activities, namely epithelial to mesenchymal transition, homotypic and heterotypic cell-cell adhesion, cell-matrix adhesion, migration, proteolysis and vesicle exocytosis, depend on branching networks of signal transduction pathways including activation of trimeric G proteins, phosphoinositide 3-kinase, src, signal transducer and activator of transcription and the Rab, Rac and Rho family of small GTPases. The role of proteolysis in invasion is not limited to breakdown of extracellular matrix but also causes cleavage of pro-angiogenic fragments from cell surface glycoproteins. Some cell types or molecules implicated in invasion-associated activities may serve as prognostic biomarker or as target for patient-tailored therapy.

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