The investigation of the role of VHL-HIF signaling in DNA repair and apoptosis in zebrafish

Abstract

<jats:title>Abstract</jats:title><jats:p>pVHL is a tumor suppressor. The lack of its function leads to various tumors, among which ccRCC (clear cell renal cell carcinoma) has the most serious outcome due to its resistance to chemotherapies and radiotherapies. Although HIF promotes the progression of ccRCC, the precise mechanism by which the loss of VHL leads to tumor initiation remains unclear. We exploited two zebrafish <jats:italic>vhl</jats:italic> mutants, <jats:italic>vhl</jats:italic> and <jats:italic>vll</jats:italic>, and <jats:italic>Tg(phd3::GFP)<jats:sup>i144</jats:sup></jats:italic> fish to identify crucial functions of Vhl in tumor initiation. Through the mutant analysis, we found that the role of pVHL in DNA repair is conserved in zebrafish Vll. Interestingly, we also discovered that Hif activation strongly suppressed genotoxic stress induced DNA repair defects and apoptosis in <jats:italic>vll</jats:italic> and <jats:italic>brca2</jats:italic> mutants and in the embryos lacking ATM activity. These results suggest the potential of HIF as a clinical modulator that can protect cells from accumulating DNA damage and apoptosis which can lead to cancers and neurodegenerative disorders.</jats:p>