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Loss of nuclear receptor RXR? in epidermal keratinocytes promotes the formation of Cdk4-activated invasive melanomas.


ABSTRACT: 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 RXR? in epidermal keratinocytes during human melanoma progression. In the absence of keratinocytic RXR?, 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, ?-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 RXR? 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.

SUBMITTER: Hyter S 

PROVIDER: S-EPMC2939934 | biostudies-literature | 2010 Oct

REPOSITORIES: biostudies-literature

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Loss of nuclear receptor RXRα in epidermal keratinocytes promotes the formation of Cdk4-activated invasive melanomas.

Hyter Stephen S   Bajaj Gaurav G   Liang Xiaobo X   Barbacid Mariano M   Ganguli-Indra Gitali G   Indra Arup Kumar AK  

Pigment cell & melanoma research 20100709 5


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  ...[more]

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