Abstract

Pleural mesothelioma (PM) is a rapidly fatal tumor. The Cancer Genome Atlas (TCGA) investigation of PM revealed that patients with activated type-I interferon (IFN) pathway have a better clinical outcome. We recently demonstrated that the expression of endogenous retroviruses (ERV) due to promoter demethylation contributes to dsRNA formation and activation of type-I IFN signaling in an experimental mouse model of mesothelioma development. The aim of this study is to investigate ERV and type-I IFN activation in human PM.

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