AI Article Synopsis

  • A study using RNA sequencing showed that BCC induction in murine skin resulted in significant gene upregulation, with treatments like AFL and the hedgehog inhibitor vismodegib reversing these changes, though vismodegib was more effective.
  • Both treatments increased immune cell infiltration in the skin, with AFL notably recruiting a larger number of immune cells, suggesting different mechanisms at play that could inform future combined treatment strategies.

Article Abstract

Recent studies have demonstrated that ablative fractional laser (AFL) can inhibit the hedgehog pathway, enhance immune infiltration and clear basal cell carcinomas (BCCs) in murine models. In this study, we applied RNA sequencing to further characterise the impact of AFL on the transcriptome of murine skin containing early-stage microscopic BCCs, contrasting it with the effects of topical application of the hedgehog inhibitor vismodegib. Our results showed that BCC induction in murine skin was primarily linked to gene upregulation (significantly upregulated genes: 277, significantly downregulated genes: 24). Characterisation of these genes with Ingenuity Pathway Analysis showed that tumour induction was associated with activation of BCC and Sonic Hedgehog signalling. Both AFL and vismodegib treatments reversed these changes, with vismodegib demonstrating superior performance by reversing most of the upregulated genes (AFL: 59/277; vismodegib: 180/277). Surprisingly, Ingenuity Pathway Analysis also revealed that both AFL and vismodegib treatments caused considerable immune cell infiltration. Based on gene set enrichment analysis and cell type deconvolution, AFL treatment resulted in the largest immune cell recruitment, which for both treatments primarily consisted of infiltrating neutrophils, macrophages and monocytes. In conclusion, the distinct effects observed in BCC skin following AFL and vismodegib treatment suggest key differences between the two interventions. Future applications of AFL or vismodegib treatments could leverage their individual effects, for example by combining the effect of AFL on the immune system with other topical treatments.

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http://dx.doi.org/10.1111/exd.15187DOI Listing

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Article Synopsis
  • A study using RNA sequencing showed that BCC induction in murine skin resulted in significant gene upregulation, with treatments like AFL and the hedgehog inhibitor vismodegib reversing these changes, though vismodegib was more effective.
  • Both treatments increased immune cell infiltration in the skin, with AFL notably recruiting a larger number of immune cells, suggesting different mechanisms at play that could inform future combined treatment strategies.
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Background: Systemically delivered hedgehog inhibitors including vismodegib and sonidegib are widely used to treat basal cell carcinomas (BCCs). Ablative fractional laser (AFL)-assisted topical delivery of vismodegib has been demonstrated in preclinical studies. The aim of this explorative clinical study was to evaluate intratumoral vismodegib concentrations and effect on hedgehog pathway gene expression following AFL-assisted topical vismodegib delivery to BCCs.

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This study aimed to investigate the impact of ablative fractional laser (AFL) on hedgehog pathway gene expression in murine microscopic basal cell carcinomas (BCCs) and compare these results to the effect of topical treatment with vismodegib, an FDA-approved hedgehog inhibitor. In 25 mice, 1 cm skin test sites (n = 44) containing microscopic BCCs were exposed to one of three interventions: a single CO AFL treatment (1 pulse, 40 mJ/microbeam, wavelength 10.6 μm, 5% density, pulse rate 250 Hz, n = 12), eight topical vismodegib treatments (3.

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Background And Objective: Hedgehog inhibitors such as vismodegib are targeted drugs widely used for the treatment of basal cell carcinomas; however, their use is significantly limited by frequent systemic side effects due to oral administration route. We aim to use ablative fractional laser (AFL) to enable the topical delivery of vismodegib to relevant dermal depths.

Materials And Methods: Pig skin was treated in vitro with a fractional 10,600 nm CO laser at 0 or 80 mJ/microbeam and exposed to vismodegib (6.

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