Dysregulation of the Sirt5/IDH2 axis contributes to sunitinib resistance in human renal cancer cells. Issue 3 (8th February 2021)
- Record Type:
- Journal Article
- Title:
- Dysregulation of the Sirt5/IDH2 axis contributes to sunitinib resistance in human renal cancer cells. Issue 3 (8th February 2021)
- Main Title:
- Dysregulation of the Sirt5/IDH2 axis contributes to sunitinib resistance in human renal cancer cells
- Authors:
- Meng, Liang
Chen, Deqiang
Meng, Gaopei
Lu, Li
Han, Chenggang - Abstract:
- Abstract : Sunitinib (Sun), a tyrosine kinase inhibitor of vascular endothelial growth factor receptor, is the standard first‐line treatment against advanced clear cell renal cell carcinoma (RCC), but resistance to therapy is inevitable. Reactive oxygen species production is associated with sensitivity to chemotherapy, but the underlying mechanisms are not completely understood. Here, we investigated the mechanisms contributing to Sun resistance using the RCC cell lines ACHN and 786‐O. We report that Sun‐resistant cells exhibited reduced apoptosis, increased cell viability, increased reactive oxygen species production and disrupted mitochondrial function. Furthermore, chronic Sun treatment resulted in an up‐regulation of Sirt5/isocitrate dehydrogenase 2 (IDH2) expression levels. Knockdown of Sirt5/IDH2 impaired mitochondrial function and partially attenuated Sun resistance. Finally, up‐regulation of Sirt5 enhanced the expression of IDH2 via modulation of succinylation at K413 and promoted protein stability. In conclusion, dysregulation of Sirt5/IDH2 partially contributes to Sun resistance in RCC cells by affecting antioxidant capacity. Abstract : Sunitinib‐resistant cells exhibited up‐regulation of Sirt5/isocitrate dehydrogenase 2 (IDH2) expression levels, which confer drug resistance. Up‐regulation of Sirt5 enhanced the expression of IDH2 via modulation of succinylation at K413 and promotion of protein stability. Dysregulation of Sirt5/IDH2 partially contributes to SunAbstract : Sunitinib (Sun), a tyrosine kinase inhibitor of vascular endothelial growth factor receptor, is the standard first‐line treatment against advanced clear cell renal cell carcinoma (RCC), but resistance to therapy is inevitable. Reactive oxygen species production is associated with sensitivity to chemotherapy, but the underlying mechanisms are not completely understood. Here, we investigated the mechanisms contributing to Sun resistance using the RCC cell lines ACHN and 786‐O. We report that Sun‐resistant cells exhibited reduced apoptosis, increased cell viability, increased reactive oxygen species production and disrupted mitochondrial function. Furthermore, chronic Sun treatment resulted in an up‐regulation of Sirt5/isocitrate dehydrogenase 2 (IDH2) expression levels. Knockdown of Sirt5/IDH2 impaired mitochondrial function and partially attenuated Sun resistance. Finally, up‐regulation of Sirt5 enhanced the expression of IDH2 via modulation of succinylation at K413 and promoted protein stability. In conclusion, dysregulation of Sirt5/IDH2 partially contributes to Sun resistance in RCC cells by affecting antioxidant capacity. Abstract : Sunitinib‐resistant cells exhibited up‐regulation of Sirt5/isocitrate dehydrogenase 2 (IDH2) expression levels, which confer drug resistance. Up‐regulation of Sirt5 enhanced the expression of IDH2 via modulation of succinylation at K413 and promotion of protein stability. Dysregulation of Sirt5/IDH2 partially contributes to Sun resistance by disturbing mitochondrial functions and affecting antioxidant capacity of renal cell carcinoma cells. … (more)
- Is Part Of:
- FEBS open bio. Volume 11:Issue 3(2021)
- Journal:
- FEBS open bio
- Issue:
- Volume 11:Issue 3(2021)
- Issue Display:
- Volume 11, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 11
- Issue:
- 3
- Issue Sort Value:
- 2021-0011-0003-0000
- Page Start:
- 921
- Page End:
- 931
- Publication Date:
- 2021-02-08
- Subjects:
- clear cell renal cell carcinoma -- desuccinylation -- isocitrate dehydrogenase 2 -- Sirt5 -- sunitinib
Molecular biology -- Periodicals
Cytology -- Periodicals
Life sciences -- Periodicals
Biological Science Disciplines -- Periodicals
Molecular Biology -- Periodicals
Cell Biology -- Periodicals
Cytology
Life sciences
Molecular biology
Periodicals
572.805 - Journal URLs:
- http://febs.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)2211-5463/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1002/2211-5463.13090 ↗
- Languages:
- English
- ISSNs:
- 2211-5463
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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