Department of Medical Treatment Cosmetology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, China.
Medical Department, The Second Affiliated Hospital of Guangxi Medical University, Nanning, China.
J Cell Mol Med. 2020 Mar;24(6):3407-3418. doi: 10.1111/jcmm.15015. Epub 2020 Jan 26.
Chemokines and their receptors have been reported to drive immune cells into tumours or to be directly involved in the promotion or inhibition of the development of tumours. However, their expression in regional lymph node (LN) tissues in melanoma patients remains unknown. The present study investigated the relationship between the expression of mRNA of chemokines and their receptors and clinicopathology of the regional LN tissues of skin cutaneous melanoma (SKCM) patients available in The Cancer Genome Atlas. The relationship between chemokines and their receptors and the composition of immune cells within the tumour was analysed. In SKCM regional LN tissues, the high expression of 32 types of chemokines and receptors, namely CCL2, 4-5, 7-8, 13, 22-25, CCR1-9, CXCL9-13, 16, CXCR3, 5, 6, XCL1-2 and XCR1 in LN was associated with favourable patient prognosis. Conversely, high expression of CXCL17 was an indicator of poor prognosis. The expression of mRNA for CXCL9-11, 13, CXCR3, 6, CCL2, 4, 5, 7, 8, 25, CCR1, 2, 5, and XCL1, 2 in regional LN tissues was positively correlated with the fraction of CD8-positive T cells and M1 macrophages, and was negatively correlated with M0 macrophages. CCR4, 6-9, CCL13, 22, 23 and XCR1 were positively correlated with the fraction of memory B cells and naive T cells, and negatively correlated with M0 macrophages and resting mast cells, suggesting that chemokines and their receptors may affect the prognosis of patients by guiding immune cells into the tumour microenvironment to eliminate tumour cells.
趋化因子及其受体已被报道可将免疫细胞驱入肿瘤,或直接参与肿瘤的促进或抑制发展。然而,它们在黑色素瘤患者区域淋巴结(LN)组织中的表达仍不清楚。本研究调查了在癌症基因组图谱(TCGA)中可获得的皮肤黑色素瘤(SKCM)患者区域 LN 组织中趋化因子及其受体的 mRNA 表达与临床病理学之间的关系。分析了趋化因子及其受体与肿瘤内免疫细胞组成之间的关系。在 SKCM 区域 LN 组织中,32 种趋化因子和受体(CCL2、4-5、7-8、13、22-25、CCR1-9、CXCL9-13、16、CXCR3、5、6、XCL1-2 和 XCR1)的高表达与患者预后良好相关。相反,CXCL17 的高表达是预后不良的指标。CXCL9-11、13、CXCR3、6、CCL2、4、5、7、8、25、CCR1、2、5 和 XCL1、2 在区域 LN 组织中的 mRNA 表达与 CD8+T 细胞和 M1 巨噬细胞的比例呈正相关,与 M0 巨噬细胞呈负相关。CCR4、6-9、CCL13、22、23 和 XCR1 与记忆 B 细胞和幼稚 T 细胞的比例呈正相关,与 M0 巨噬细胞和静止肥大细胞呈负相关,提示趋化因子及其受体可能通过引导免疫细胞进入肿瘤微环境来消除肿瘤细胞,从而影响患者的预后。