Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR, USA.
Pigment Cell Melanoma Res. 2010 Oct;23(5):635-48. doi: 10.1111/j.1755-148X.2010.00732.x. Epub 2010 Jul 9.
Keratinocytes contribute to melanocyte transformation by affecting their microenvironment, in part through the secretion of paracrine factors. Here we report a loss of expression of nuclear receptor RXRα in epidermal keratinocytes during human melanoma progression. In the absence of keratinocytic RXRα, in combination with mutant Cdk4, cutaneous melanoma was generated that metastasized to lymph nodes in a bigenic mouse model. Expression of several keratinocyte-derived mitogenic growth factors (Et-1, Hgf, Scf, α-MSH and Fgf 2 ) was elevated in skin of bigenic mice, whereas Fas, E-cadherin and Pten, implicated in apoptosis, cellular invasion and melanomagenesis, respectively, were downregulated within the microdissected melanocytic tumors. We demonstrated that RXRα is recruited on the proximal promoter of both Et-1 and Hgf, possibly directly regulating their transcription in keratinocytes. These studies demonstrate the contribution of keratinocytic paracrine signaling during the cellular transformation and malignant conversion of melanocytes.
角质形成细胞通过影响黑素细胞的微环境来促进黑素细胞的转化,部分是通过旁分泌因子的分泌。在这里,我们报告了在人类黑色素瘤进展过程中,表皮角质形成细胞中核受体 RXRα 的表达缺失。在缺乏角质形成细胞 RXRα 的情况下,与突变型 Cdk4 结合,在双基因小鼠模型中产生了转移性皮肤黑色素瘤。在双基因小鼠的皮肤中,几种由角质形成细胞衍生的促有丝分裂生长因子(内皮素-1、HGF、干细胞因子、α-MSH 和 FGF-2)的表达升高,而 Fas、E-钙粘蛋白和 Pten,分别涉及细胞凋亡、细胞侵袭和黑色素瘤发生,在微切割的黑素瘤肿瘤中下调。我们证明了 RXRα 被募集到 Et-1 和 HGF 的近端启动子上,可能直接调节它们在角质形成细胞中的转录。这些研究表明了角质形成细胞旁分泌信号在黑素细胞的细胞转化和恶性转化中的作用。