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黑素细胞性病变中趋化因子受体的概况:CXCR6在黑色素瘤中的从头表达

Profiles of chemokine receptors in melanocytic lesions: de novo expression of CXCR6 in melanoma.

作者信息

Seidl Hannes, Richtig Erika, Tilz Hemma, Stefan Martina, Schmidbauer Ulrike, Asslaber Martin, Zatloukal Kurt, Herlyn Meenhard, Schaider Helmut

机构信息

Department of Dermatology, Tumor Biology Unit, Medical University of Graz, Graz, Austria.

出版信息

Hum Pathol. 2007 May;38(5):768-80. doi: 10.1016/j.humpath.2006.11.013. Epub 2007 Feb 15.

Abstract

Selective expression of certain chemokine receptors by melanoma cells and the presence of their ligands in tissues might govern organ site-specific metastasis. Because the expression profile of chemokine receptors in tissues of melanocytic origin is unknown, we performed a comprehensive study on melanocytic tissue samples investigating the expression of 18 chemokine receptors at the mRNA level by real-time polymerase chain reaction, using a semiquantitative approach, and of 3 chemokine receptors (CXCR6, CCR9, and XCR1) at the protein level. We report on the de novo expression of CXCR6 in primary melanomas and melanoma metastases, but absence in melanoma cell lines and congenital nevi. CXCR4 and CCR1 were the only 2 chemokine receptors that were consistently expressed in melanocytes, melanoma cell lines, primary, and metastatic melanoma; CCR1 expression increased significantly over progression. CCR9 and XCR1 transcripts were found in melanocytic lesions, and expression was confirmed by immunohistochemistry. Transcripts for CCR10 were not found in any of the lesions, but in some melanoma cell lines. Expression of CCR7 was observed in primary melanomas and some metastases. CCR5 was exclusively expressed in primary melanomas and some cutaneous metastases. Results revealed a restricted and differential pattern of chemokine receptor expression in melanoma tissue, which varies substantially from the expression profile of melanoma cell lines and warrants functional studies on some receptors.

摘要

黑色素瘤细胞对某些趋化因子受体的选择性表达以及其配体在组织中的存在可能决定了器官位点特异性转移。由于黑素细胞起源组织中趋化因子受体的表达谱尚不清楚,我们对黑素细胞组织样本进行了一项全面研究,采用半定量方法通过实时聚合酶链反应在mRNA水平上研究18种趋化因子受体的表达,并在蛋白质水平上研究3种趋化因子受体(CXCR6、CCR9和XCR1)的表达。我们报告了CXCR6在原发性黑色素瘤和黑色素瘤转移灶中的从头表达,但在黑色素瘤细胞系和先天性痣中不存在。CXCR4和CCR1是仅有的在黑素细胞、黑色素瘤细胞系、原发性和转移性黑色素瘤中持续表达的2种趋化因子受体;CCR1的表达在进展过程中显著增加。在黑素细胞病变中发现了CCR9和XCR1转录本,并通过免疫组织化学证实了其表达。在任何病变中均未发现CCR10的转录本,但在一些黑色素瘤细胞系中发现了。在原发性黑色素瘤和一些转移灶中观察到CCR7的表达。CCR5仅在原发性黑色素瘤和一些皮肤转移灶中表达。结果显示黑色素瘤组织中趋化因子受体表达存在受限且有差异的模式,这与黑色素瘤细胞系的表达谱有很大不同,因此需要对一些受体进行功能研究。

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