Chronic Inflammation in Skin Malignancies

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DOI:

https://doi.org/10.5334/1750-2187-11-2

Keywords:

inflammation, skin cancer, cytokine, cancer immunotherapy

Abstract

Chronic inflammation is linked to the development and progression of multiple cancers, including those of the lung, stomach, liver, colon, breast and skin. Inflammation not only drives the oncogenic transformation of epithelial cells under the stress of chronic infection and autoimmune diseases, but also promotes the growth, progression and metastatic spread of cancers. Tumor-infiltrating inflammatory cells are comprised of a diverse population of myeloid and immune cell types, including monocytes, macrophages, dendritic cells, T and B cells, and others. Different myeloid and lymphoid cells within tumor microenvironment exert diverse, often contradicting, effects during skin cancer development and progression. The nature of tumor-immune interaction determines the rate of cancer progression and the outcome of cancer treatment. Inflammatory environment within skin tumor also inhibits naturally occurring anti-tumor immunity and limits the efficacy of cancer immunotherapy. In this article we aim to give an overview on the mechanism by which inflammation interferes with the development and therapeutic intervention of cancers, especially those of the skin.

Author Biography

Kepeng Wang, University of Connecticut Health Center

Kepeng worked on the role of inflammation in cancer development and found that disrupted epithelial barrier mechanism in early colorectal tumor cells results in infiltration of gut bacteria and their products into tumor stroma, leading to tumor elicited inflammation and up-regulation of IL-23 in tumor associated macrophages. IL-23 in turn promotes the development and progression of colorectal cancer by controlling the production of inflammatory cytokines including IL-6 and IL-17. Kepeng is currently working on the mechanism of IL-17 in promoting colorectal cancer development and found that the cytokine signaling directly on tumor cells to promote the growth of early aberrant foci by activating cell growth and survival.

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Published

2016-05-05

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