Baryla Izabela, Pluciennik Elzbieta, Kośla Katarzyna, Wojcik Marzena, Zieleniak Andrzej, Zurawska-Klis Monika, Cypryk Katarzyna, Wozniak Lucyna Alicja, Bednarek Andrzej K
Department of Molecular Carcinogenesis, Medical University of Lodz, Lodz, Poland.
Department of Structural Biology, Medical University of Lodz, Lodz, Poland.
PeerJ. 2021 Jan 14;9:e10604. doi: 10.7717/peerj.10604. eCollection 2021.
Although the WW-domain-containing oxidoreductase (WWOX)/Hypoxia-inducible factor 1 (HIF1) pathway is a well-known regulator of cellular glucose and energy metabolism in pathophysiological processes, its role in gestational diabetes mellitus (GDM), remains elusive. We undertook this study to determine the effect of WWOX/HIF1A signaling on the expression of glucose metabolism genes in GDM patients.
Leukocytes were obtained from 135 pregnant women with ( = 98) or without ( = 37) GDM and, in turn, 3 months ( = 8) and 1 year ( = 12) postpartum. Quantitative RT-PCR was performed to determine gene expression profiles of the WWOX/HIF1A-related genes, including those involved in glucose transport (), glycolytic pathway (), Wnt pathway (), and inflammatory response ().
GDM patients displayed a significant downregulation of with simultaneous upregulation of which resulted in approximately six times reduction in ratio. As a consequence, induced genes () were found to be overexpressed in GDM compared to normal pregnancy and negative correlate with ratio. The postpartum expression was higher than during GDM, but its level was comparable to that observed in normal pregnancy.
The obtained results suggest a significant contribution of the gene to glucose metabolism in patients with gestational diabetes. Decreased expression in GDM compared to normal pregnancy, and in particular reduction of ratio, indicate that WWOX modulates HIF1α activity in normal tissues as described in the tumor. The effect of HIF1α excessive activation is to increase the expression of genes encoding proteins directly involved in the glycolysis which may lead to pathological changes in glucose metabolism observed in gestational diabetes.
尽管含WW结构域的氧化还原酶(WWOX)/缺氧诱导因子1(HIF1)通路是病理生理过程中细胞葡萄糖和能量代谢的著名调节因子,但其在妊娠期糖尿病(GDM)中的作用仍不清楚。我们进行了这项研究,以确定WWOX/HIF1A信号对GDM患者葡萄糖代谢基因表达的影响。
从135名患有(n = 98)或未患(n = 37)GDM的孕妇中获取白细胞,随后在产后3个月(n = 8)和1年(n = 12)时再次获取。进行定量逆转录聚合酶链反应(qRT-PCR)以确定WWOX/HIF1A相关基因的基因表达谱,包括参与葡萄糖转运()、糖酵解途径()、Wnt途径()和炎症反应()的基因。
GDM患者显示出显著下调,同时上调,导致比值降低约六倍。因此,与正常妊娠相比,GDM中诱导基因()被发现过度表达,并且与比值呈负相关。产后表达高于GDM期间,但其水平与正常妊娠时观察到的水平相当。
所得结果表明基因对妊娠期糖尿病患者的葡萄糖代谢有显著贡献。与正常妊娠相比,GDM中表达降低,特别是比值降低,表明WWOX在正常组织中调节HIF1α活性,如在肿瘤中所描述的那样。HIF1α过度激活的作用是增加编码直接参与糖酵解的蛋白质的基因的表达,这可能导致妊娠期糖尿病中观察到的葡萄糖代谢的病理变化。