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人类血小板与肿瘤细胞的相互作用因肿瘤细胞系而异。

Human platelet-tumor cell interactions vary with the tumor cell lines.

作者信息

Camez A, Dupuy E, Bellucci S, Calvo F, Bryckaert M C, Tobelem G

出版信息

Invasion Metastasis. 1986;6(6):321-34.

PMID:3100472
Abstract

Platelets may promote the development of metastasis, and tumor cells that aggregate platelets are believed to be more malignant. We studied three different human mammary carcinoma cell lines, which had different interactions with human platelet-rich plasma (PRP). The MCF-7 and the T47-D cell lines induced an adenosine diphosphate (ADP)-mediated platelet aggregation. The third cell line, MDA-MB 231 did not induce any platelet aggregation. On the contrary, this cell line inhibited ADP- and arachidonic acid-induced platelet aggregation. This inhibiting activity is mainly adenosine-mediated. The mechanism by which platelets may contribute to the dissemination of cancer could be related to platelet growth factors. MCF-7 and T47-D cell lines induced a release of platelet-derived growth factor (PDGF). On the contrary, the MDA-MB 231 cell line did not induce any platelet release. The role of these platelet growth factors in tumor cell growth is discussed.

摘要

血小板可能促进转移的发展,并且聚集血小板的肿瘤细胞被认为更具恶性。我们研究了三种不同的人乳腺癌细胞系,它们与富含人血小板的血浆(PRP)有不同的相互作用。MCF-7和T47-D细胞系诱导二磷酸腺苷(ADP)介导的血小板聚集。第三种细胞系MDA-MB 231不诱导任何血小板聚集。相反,该细胞系抑制ADP和花生四烯酸诱导的血小板聚集。这种抑制活性主要由腺苷介导。血小板可能促进癌症扩散的机制可能与血小板生长因子有关。MCF-7和T47-D细胞系诱导血小板衍生生长因子(PDGF)的释放。相反,MDA-MB 231细胞系不诱导任何血小板释放。讨论了这些血小板生长因子在肿瘤细胞生长中的作用。

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