| RRC ID |
69911
|
| 著者 |
Emberley E, Pan A, Chen J, Dang R, Gross M, Huang T, Li W, MacKinnon A, Singh D, Sotirovska N, Steggerda SM, Wang T, Parlati F.
|
| タイトル |
The glutaminase inhibitor telaglenastat enhances the antitumor activity of signal transduction inhibitors everolimus and cabozantinib in models of renal cell carcinoma.
|
| ジャーナル |
PLoS One
|
| Abstract |
Dysregulated metabolism is a hallmark of cancer that manifests through alterations in bioenergetic and biosynthetic pathways to enable tumor cell proliferation and survival. Tumor cells exhibit high rates of glycolysis, a phenomenon known as the Warburg effect, and an increase in glutamine consumption to support the tricarboxylic acid (TCA) cycle. Renal cell carcinoma (RCC) tumors express high levels of glutaminase (GLS), the enzyme required for the first step in metabolic conversion of glutamine to glutamate and the entry of glutamine into the TCA cycle. We found that RCC cells are highly dependent on glutamine for proliferation, and this dependence strongly correlated with sensitivity to telaglenstat (CB-839), an investigational, first-in-class, selective, orally bioavailable GLS inhibitor. Metabolic profiling of RCC cell lines treated with telaglenastat revealed a decrease in glutamine consumption, which was concomitant with a decrease in the production of glutamate and other glutamine-derived metabolites, consistent with GLS inhibition. Treatment of RCC cells with signal transduction inhibitors everolimus (mTOR inhibitor) or cabozantinib (VEGFR/MET/AXL inhibitor) in combination with telaglenastat resulted in decreased consumption of both glucose and glutamine and synergistic anti-proliferative effects. Treatment of mice bearing Caki-1 RCC xenograft tumors with cabozantinib plus telaglenastat resulted in reduced tumor growth compared to either agent alone. Enhanced anti-tumor activity was also observed with the combination of everolimus plus telaglenastat. Collectively, our results demonstrate potent, synergistic, anti-tumor activity of telaglenastat plus signal transduction inhibitors cabozantinib or everolimus via a mechanism involving dual inhibition of glucose and glutamine consumption.
|
| 巻・号 |
16(11)
|
| ページ |
e0259241
|
| 公開日 |
2021-1-1
|
| DOI |
10.1371/journal.pone.0259241
|
| PII |
PONE-D-20-39834
|
| PMID |
34731180
|
| PMC |
PMC8565744
|
| MeSH |
Anilides / administration & dosage*
Anilides / pharmacology
Animals
Benzeneacetamides / administration & dosage*
Benzeneacetamides / pharmacology
Carcinoma, Renal Cell / drug therapy*
Carcinoma, Renal Cell / metabolism
Cell Line, Tumor
Cell Proliferation / drug effects
Cell Survival / drug effects
Drug Synergism
Everolimus / administration & dosage*
Everolimus / pharmacology
Female
Gene Expression Regulation, Neoplastic / drug effects
Glucose / metabolism
Glutaminase / antagonists & inhibitors
Glutamine / metabolism
Humans
Kidney Neoplasms / drug therapy*
Kidney Neoplasms / metabolism
Mice
Pyridines / administration & dosage*
Pyridines / pharmacology
Signal Transduction / drug effects
Thiadiazoles / administration & dosage*
Thiadiazoles / pharmacology
Xenograft Model Antitumor Assays
|
| IF |
2.74
|
| リソース情報 |
| ヒト・動物細胞 |
TUHR10TKB(RCB1275)
OS-RC-2(RCB0735)
RCC10RGB(RCB1151) |
