4.7 Article

Sunitinib versus Pazopanib Dilemma in Renal Cell Carcinoma: New Insights into the In Vitro Metabolic Impact, Efficacy, and Safety

期刊

出版社

MDPI
DOI: 10.3390/ijms23179898

关键词

metastatic renal cell carcinoma; tyrosine kinase inhibitors; toxicity; oxidative stress; metabolomics; H-1 NMR spectroscopy; endometabolome; exometabolome

资金

  1. FEDER-Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020-Operacional Programme for Competitiveness and Internationalisation (POCI)
  2. Portuguese funds through FCT-Fundacao para a Ciencia e a Tecnologia [POCI-01-0145-FEDER-030388-PTDC/SAU-SER/30388/2017]
  3. FCT [UI/BD/151313/2021, UIDP/04378/2020, UIDB/04378/2020]
  4. Associate Laboratory Institute for Health and Bioeconomy-i4HB [LA/P/0140/2020]
  5. Fundação para a Ciência e a Tecnologia [UI/BD/151313/2021] Funding Source: FCT

向作者/读者索取更多资源

This study compared the different cellular and metabolic responses of sunitinib and pazopanib in treating metastatic renal cell carcinoma, suggesting that sunitinib has better in vitro efficacy against target RCC cells and lesser nephrotoxic potential than pazopanib.
Sunitinib and pazopanib are tyrosine kinase inhibitors (TKIs) used as first-line therapy for metastatic renal cell carcinoma (RCC). Although these TKIs are associated with similar survival outcomes, some differences have been reported in their safety profiles. In this work, traditional toxicological endpoints (cell viability and growth, oxidative stress, and nuclear morphology) and H-1 NMR spectroscopy-based metabolomics analysis were used to provide new insights into the cytotoxicity and metabolic mechanisms underlying sunitinib and pazopanib treatments. Tumoral (Caki-1) and non-tumoral (HK-2) human renal cells were exposed to clinically relevant concentrations of sunitinib (2 mu M) or pazopanib (50 mu M). Sunitinib showed selectivity for cancer cells, inhibiting proliferation, and inducing apoptotic death of Caki-1 cells, whereas pazopanib had a similar cytotoxic effect in both tumoral and non-tumoral cells. H-1-NMR metabolomics unveiled a higher impact of sunitinib on the levels of intracellular metabolites of Caki-1 cells (seven dysregulated metabolites), suggesting dysregulations on amino acid, glutathione and glycerophospholipid metabolisms. In contrast, pazopanib had a higher impact on the levels of extracellular metabolites of Caki-1 cells (seven dysregulated metabolites in culture medium), unveiling alterations on amino acid and energetic metabolisms. In HK-2 cells, sunitinib caused only a minor increase in intracellular isoleucine levels, whereas pazopanib induced several alterations on the intracellular (three dysregulated metabolites) and extracellular (three dysregulated metabolites) compartments suggesting changes on amino acid, glycerophospholipid, and energy metabolisms. Our results demonstrate that these TKIs elicit distinct cellular and metabolic responses, with sunitinib showing better in vitro efficacy against target RCC cells and lesser nephrotoxic potential than pazopanib.

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