Senescent fibroblasts can drive melanoma initiation and progression

TL;DR

This study uses a hybrid multiscale model and experiments to show that senescent fibroblasts in the skin microenvironment promote melanoma initiation and progression by creating a pro-oncogenic environment.

Contribution

It introduces a novel hybrid multiscale model of skin that incorporates senescent fibroblasts, revealing their role in melanoma development and potential as therapeutic targets.

Findings

Senescent fibroblasts promote melanoma cell growth and invasion.

Increased proteolytic activity observed near melanoma lesions.

Senescent fibroblasts create a pro-oncogenic skin microenvironment.

Abstract

Skin is one of the largest human organ systems whose primary purpose is the protection of deeper tissues. As such, the skin must maintain a homeostatic balance in the face of many microenvironmental and genetic perturbations. At its simplest, skin homeostasis is maintained by the balance between skin cell growth and death such that skin architecture is preserved. This study presents a hybrid multiscale mathematical model of normal skin (vSkin). The model focuses on key cellular and microenvironmental variables that regulate homeostatic interactions among keratinocytes, melanocytes and fibroblasts, key components of the skin. The model recapitulates normal skin structure, and is robust enough to withstand physical as well as biochemical perturbations. Furthermore, the vSkin model revealed the important role of the skin microenvironment in melanoma initiation and progression. Our experiments showed that dermal fibroblasts, which are an important source of growth factors in the skin, adopt a phenotype that facilitates cancer cell growth and invasion when they become senescent. Based on these experimental results, we incorporated senescent fibroblasts into vSkin model and showed that senescent fibroblasts transform the skin microenvironment and enhance the growth and invasion of normal melanocytes as well as early stage melanoma cells. These predictions are consistent with our experimental results as well as clinical observations. Our co-culture experiments show that the senescent fibroblasts promote the growth and invasion of non-tumorigenic melanoma cells. We also observed increased proteolytic activity in stromal fields adjacent to melanoma lesions in human histology. Collectively, senescent fibroblasts create a pro-oncogenic environment that synergizes with mutations to drive melanoma initiation and progression and should therefore be considered as a potential future therapeutic target.