Helge Waldum- Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway
HIF and renal cancer
Treatment of anemia due to chronic kidney disease with agents increasing erythropoietin (EPO) from erythropoietin producing cell (EPC) by inhibition of one of the enzymes causing degradation of hypoxia inducible factor (HIF) (HIF prolyl hydroxylase inhibitor (HIF-PHI)) is gaining popularity (Chen et al., 2022). It is, however, well-known that a small proportion of patients with clear cell renal cell cancer (CCRCC) has erythrocytosis and a larger part EPO production in the cancer cells (Palapattu et al., 2002; Wiesener et al., 2007). In a study applying immunohistochemistry with high sensitivity we found that practically all CCRCCs expressed erythropoietin as well as the neuroendocrine marker neuron-specific enolase (NSE) (Mjønes et al., 2017), the latter a marker with hitherto misrecognized reputation.We concluded that CCRCC (the dominating histological type of kidney cancer) (Mjønes et al., 2017; Waldum et al., 2022) originated from the EPC. There are many features in CCRCC in common with neuroendocrine tumours (Waldum et al., 2022). HIF is a major stimulator of EPO production, whereas von-Hippel Lindau factor is central in HIF degradation. Dysfunction of von-Hippel Lindau factor is an important factor in CCRCC demonstrating the role of HIF in renal carcinogenesis (Gnarra et al., 1994). There is generally a close correlation between stimulation of the function and proliferation of a cell. Chronic overstimulation of the cell of origin (whether a tubular cell or based upon our study, the EPO cell) by HIF predisposes to renal cancer in von-Hippel Lindau syndrome (Ohh et al., 2022). and it is reason to fear that increased stimulation of the EPO cell by elevated HIF due to inhibited degradation by HIF-PHI inhibitors including roxadustat, could in long-term predispose to CCRCC. The importance of long-term hyperstimulation by HIF in renal carcinogenesis is demonstrated by the latency of renal cancer even in patients with congenital von-Hippel Lindau syndrome. However, there is no study describing any neoplastic renal changes in human secondary to roxadustat although growth of renal cysts has been reported (Zhu et al., 2022). Lack of neoplastic renal changes in long-term rodent studies are also reassuring although the dosing of roxadustat was difficult due to rapid clearance. Although toxicology studies hitherto seem reassuring, taking into consideration the long latency for neoplasia in general, there is every reason to be vigilante concerning long-term use of agents inducing increased HIF exposure.
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Keywords: von Hippel Lindau factor, hypoxia inducible factor (HIF), renal cancer, prolyl hydroxylase inhibitor (roxadustat), renal anemia, erythropoietin producing cell
Citation: Waldum H (2023) Dysfunction of von-Hippel Lindau factor causes reduced degradation of HIF leading to renal cancer. Hypoxia-inducible factor-prolyl hydroxylase enzyme inhibitors also lessen HIF destruction and could therefore increase renal cancer. Front. Pharmacol. 14:1170796. doi: 10.3389/fphar.2023.1170796
Received: 21 February 2023; Accepted: 26 May 2023;
Published: 06 June 2023.
Edited by:
Giuseppe Remuzzi, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, ItalyReviewed by:
Marco Allinovi, Careggi University Hospital, ItalyCopyright © 2023 Waldum. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Helge Waldum, helge.waldum@ntnu.no