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趋化因子在黑色素瘤进展中的作用

[Role of chemokines in melanoma progression].

作者信息

Monteagudo C, Pellín-Carcelén A, Martín J M, Ramos D

机构信息

Departamento de Patología, Universidad de Valencia, España.

出版信息

Actas Dermosifiliogr. 2011 Sep;102(7):498-504. doi: 10.1016/j.ad.2011.03.004. Epub 2011 Apr 30.

Abstract

Metastasis is the main cause of death from melanoma. Chemokines are low molecular weight chemotactic cytokines that facilitate cellular migration. Thus, cells that express receptors for a given chemokine are attracted to the site of its production. As certain chemokines are found in abundance in organs that are common targets of metastasis and receptors for these chemokines are expressed by tumor cells, it was hypothesized that chemokine gradients might selectively facilitate metastasis to these organs. A later finding that these chemokines were produced by tumor cells, with evidence of autocrine effects, obliged the modification of that hypothesis. Many chemokines are also known to have opposing effects according to the type of cell they are acting on (tumor, inflammatory/immune, or endothelial cells), their functional status, or interactions with other molecules. The expression of chemokines and their receptors by melanoma cells enhances tumor progression by altering their microenvironment, stimulating angiogenesis, and inhibiting the immune response.

摘要

转移是黑色素瘤致死的主要原因。趋化因子是促进细胞迁移的低分子量趋化性细胞因子。因此,表达特定趋化因子受体的细胞会被吸引到其产生的部位。由于在转移的常见靶器官中发现某些趋化因子大量存在,且肿瘤细胞表达这些趋化因子的受体,因此有人推测趋化因子梯度可能会选择性地促进向这些器官的转移。后来发现这些趋化因子由肿瘤细胞产生,并存在自分泌效应的证据,这就需要对该假说进行修正。还已知许多趋化因子根据其作用的细胞类型(肿瘤细胞、炎症/免疫细胞或内皮细胞)、功能状态或与其他分子的相互作用而具有相反的作用。黑色素瘤细胞趋化因子及其受体的表达通过改变其微环境、刺激血管生成和抑制免疫反应来促进肿瘤进展。

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