Citations
1 publicationsPublications from researchers using this productDescription
Telaglenastat (CB-839) is a reversible, orally bioavailable glutaminase 1 (GLS1) inhibitor that induces autophagy and has antitumor activity[1]. Compared to GLS2, Telaglenastat selectively inhibits the GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C)[2]. The IC50 values of Telaglenastat for endogenous glutaminase in mouse kidney and brain are 23nM and 28nM, respectively.
Telaglenastat(0.1-1000nM; 72 hours) had antiproliferative activity in HCC1806 and MDA-MB-231 cells with IC50s of 49nM and 26nM, respectively[1].Telaglenastat (1μM; 72 hours) activated caspase 3/7 and induced apoptosis in MDA-MB-231 and HCC1806 cells[1].
Telaglenastat (200mg/kg; p.o.; twice daily for 28 days) had antitumor activity in mice xenograft models of TNBC[1].
References:
[1]. Gross MI, et al. Antitumor activity of the glutaminase inhibitor CB-839 in triple-negative breast cancer. Mol Cancer Ther. 2014 Apr;13(4):890-901.
[2]. Biancur DE, et al. Compensatory metabolic networks in pancreatic cancers upon perturbation of glutaminemetabolism. Nat Commun. 2017 Jul 3;8:15965.
Protocol
| Cell experiment [1]: | |
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Cell lines |
TNBC cell lines HCC1806 and MDA-MB-231, T47D cell line |
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Preparation method |
Soluble in DMSO. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months. |
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Reacting condition |
1 μmol/L, 4 hours |
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Applications |
CB-839 treatment showed a potent effect on the proliferation of HCC1806 and MDA-MB-231 cells with the IC50 of 20–55 nmol/L. CB-839 (1 μmol/L) inhibited the metabolism of glutamine, the rates of glutamine consumption and glutamate production in HCC1806 and T47D cell lines. TNBC cell lines exhibited greater sensitivity as measured by the extent of cell growth or cell loss following treatment with 1 μmol/L CB-839 for 72 hours. CB-839 (1 μmol/L, 72 hours) showed antiproliferative activity on breast cancer cell lines. |
| Animal experiment [1]: | |
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Animal models |
Scid/Beige mice bearing orthotopically implanted HCC1806 tumors, Patient-derived TNBC and JIMT-1 cell line xenograft models |
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Dosage form |
Oral administration, 200 mg/kg, twice daily |
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Application |
In primary patient-derived TNBC mouse model, oral dosing of single agent CB-839 (200 mg/kg twice daily) suppressed tumor growth. In the mouse JIMT-1 xenograft model, oral dosing of CB-839 alone (200 mg/kg twice daily) resulted in 54% tumor growth inhibition (TGI). Combination of CB-839 (200 mg/kg, p.o.) with paclitaxel (10 mg/kg, p.o.) largely suppressed the regrowth of the tumors resulting in a TGI relative to vehicle control of 100%. |
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Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
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References: [1]. Gross M I, Demo S D, Dennison J B, et al. Antitumor activity of the glutaminase inhibitor CB-839 in triple-negative breast cancer[J]. Molecular cancer therapeutics, 2014, 13(4): 890-901. |
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Product Documents
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