Exp Dermatol. 2011 Dec;20(12):1020-2. doi: 10.1111/j.1600-0625.2011.01377.x. Epub 2011 Oct 13.
The coincidence of skin tumors and elevated mast cell (MC) numbers has been known for many years. However, it has remained controversial whether, in this context, MCs promote or inhibit tumor growth. Addressing this problem, different melanoma and squamous cell carcinoma cell lines were co-cultivated with primary, dermal MC for 24 h and gene or protein expression of cytokines tumor necrosis factor (TNF-α), interleukin-6 (IL-6) and interleukin-8 (IL-8) estimated. Co-culture with MCs led to an increase in IL-8 gene expression and IL-8 protein release from melanoma cells and IL-6 and IL-8 gene expression and protein release from squamous cell carcinoma cells, respectively. Moreover induction of IL-6 and IL-8 was primarily regulated by MC-derived TNF-α. Our data suggest an interplay between MCs and tumor cells, which results in altered cytokine release and may, thus, have an impact on tumor growth, invasion and neovascularisation.
皮肤肿瘤与 mast cell(MC)数量升高的巧合现象已为人所知多年。然而,MC 是否促进或抑制肿瘤生长,在这方面一直存在争议。为了解决这个问题,我们将不同的黑色素瘤和鳞状细胞癌细胞系与原代真皮 MC 共同培养 24 小时,并评估细胞因子肿瘤坏死因子(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的基因或蛋白表达。与 MC 共培养导致黑色素瘤细胞中 IL-8 基因表达和 IL-8 蛋白释放增加,以及鳞状细胞癌细胞中 IL-6 和 IL-8 基因表达和蛋白释放增加。此外,IL-6 和 IL-8 的诱导主要受 MC 衍生的 TNF-α调节。我们的数据表明 MC 和肿瘤细胞之间存在相互作用,导致细胞因子释放改变,从而可能对肿瘤生长、侵袭和新生血管形成产生影响。