Marrapodi Ramona, Kovacs Daniela, Migliano Emilia, Caputo Silvia, Papaccio Federica, Pallara Tiziano, Cota Carlo, Bellei Barbara
Laboratory of Cutaneous Physiopathology and Integrated Center of Metabolomics Research, San Gallicano Dermatological Institute, IRCCS, 00144 Rome, Italy.
Department of Plastic and Regenerative Surgery, San Gallicano Dermatological Institute, IRCCS, 00144 Rome, Italy.
Int J Mol Sci. 2025 Aug 15;26(16):7901. doi: 10.3390/ijms26167901.
The Tumour Microenvironment (TME) is pivotal for melanoma progression and contributes to therapy resistance. While dermal cell involvement is well established, the role of epidermal cells remains less defined. To explore the contribution of Normal Human Keratinocytes (NHKs) to melanoma biology, we investigated the modification of gene and protein expression of NHKs exposed to melanoma-conditioned medium or maintained in a co-culture system. The analysis focused on pathways related to proliferation, inflammation, Extracellular Matrix (ECM) remodelling, and cell adhesion. Due to the well-documented melanoma-fibroblast crosstalk, Normal Human Fibroblasts (NHFs) and Cancer-Associated Fibroblasts (CAFs) were used as comparative references. Keratinocyte gene expression changes under the influence of melanoma secretome only partially overlapped with those of NHFs and CAFs, indicating cell-type-specific responses. Exposure to melanoma-conditioned medium induced the upregulation of bFGF, CXCL-16, TIMP-2, and E-cadherin in NHKs, alongside downregulating TGF-β and MMP-9. Although bFGF is a recognized pro-tumorigenic factor, the modulation of CXCL-16, TIMP-2, and TGF-β may reflect a protective response. Notably, under co-culture conditions, NHKs exhibited a pronounced pro-inflammatory and ECM-remodelling phenotype, characterized by elevated production of cytokines (IL-1α, IL-1β, and IL-8) and ECM-degrading enzymes (MMP-7, 9, 12, and 13), indicative of a pro-tumoral feature. Collectively, these findings underscore an active role for NHKs in melanoma initiation and progression.
肿瘤微环境(TME)对黑色素瘤的进展至关重要,并导致治疗抵抗。虽然真皮细胞的参与已得到充分证实,但表皮细胞的作用仍不太明确。为了探究正常人角质形成细胞(NHK)对黑色素瘤生物学的贡献,我们研究了暴露于黑色素瘤条件培养基或维持在共培养系统中的NHK的基因和蛋白质表达变化。分析聚焦于与增殖、炎症、细胞外基质(ECM)重塑和细胞黏附相关的信号通路。由于黑色素瘤与成纤维细胞之间的相互作用已有充分记录,因此将正常人成纤维细胞(NHF)和癌症相关成纤维细胞(CAF)用作比较参考。黑色素瘤分泌组影响下的角质形成细胞基因表达变化仅部分与NHF和CAF的变化重叠,表明存在细胞类型特异性反应。暴露于黑色素瘤条件培养基会诱导NHK中bFGF、CXCL-16、TIMP-2和E-钙黏蛋白的上调,同时下调TGF-β和MMP-9。虽然bFGF是一种公认的促肿瘤因子,但CXCL-16、TIMP-2和TGF-β的调节可能反映了一种保护反应。值得注意的是,在共培养条件下,NHK表现出明显的促炎和ECM重塑表型,其特征是细胞因子(IL-1α、IL-1β和IL-8)和ECM降解酶(MMP-7、9、12和13)的产生增加,表明具有促肿瘤特征。总的来说,这些发现强调了NHK在黑色素瘤起始和进展中的积极作用。