A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Hypoxia-inducible factor (HIF)-prolyl hydroxylase 3 (PHD3) maintains high HIF2A mRNA levels in clear cell renal cell carcinoma




TekijätMiikkulainen Petra, Högel Heidi, Seyednasrollah Fatemeh, Rantanen Krista, Elo Laura L., Jaakkola Panu M.

KustantajaAMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Julkaisuvuosi2019

JournalJournal of Biological Chemistry

Tietokannassa oleva lehden nimiJOURNAL OF BIOLOGICAL CHEMISTRY

Lehden akronyymiJ BIOL CHEM

Vuosikerta294

Numero10

Aloitussivu3760

Lopetussivu3771

Sivujen määrä12

ISSN0021-9258

eISSN1083-351X

DOIhttps://doi.org/10.1074/jbc.RA118.004902

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/39919058


Tiivistelmä
Most clear cell renal cell carcinomas (ccRCCs) have inactivation of the von Hippel-Lindau tumor suppressor protein (pVHL), resulting in the accumulation of hypoxia-inducible factor -subunits (HIF-) and their downstream targets. HIF-2 expression is particularly high in ccRCC and is associated with increased ccRCC growth and aggressiveness. In the canonical HIF signaling pathway, HIF-prolyl hydroxylase 3 (PHD3) suppresses HIF-2 protein by post-translational hydroxylation under sufficient oxygen availability. Here, using immunoblotting and immunofluorescence staining, qRT-PCR, and siRNA-mediated gene silencing, we show that unlike in the canonical pathway, PHD3 silencing in ccRCC cells leads to down-regulation of HIF-2 protein and mRNA. Depletion of other PHD family members had no effect on HIF-2 expression, and PHD3 knockdown in non-RCC cells resulted in the expected increase in HIF-2 protein expression. Accordingly, PHD3 knockdown decreased HIF-2 target gene expression in ccRCC cells and expression was restored upon forced HIF-2 expression. The effect of PHD3 depletion was pinpointed to HIF2A mRNA stability. In line with these in vitro results, a strong positive correlation of PHD3 and HIF2A mRNA expression in ccRCC tumors was detected. Our results suggest that in contrast to the known negative regulation of HIF-2 in most cell types, high PHD3 expression in ccRCC cells maintains elevated HIF-2 expression and that of its target genes, which may enhance kidney cancer aggressiveness.

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