Abstract | PURPOSE: EXPERIMENTAL DESIGN: The activity of GTx-134 as a single agent and in combination was tested in MM cell lines and primary patient samples. Downstream effector proteins and correlation with apoptosis was evaluated. Cytotoxcity in bone marrow stroma coculture experiments was assessed. Finally, the in vivo efficacy was evaluated in a human myeloma xenograft model. RESULTS:
GTx-134 inhibited the growth of 10 of 14 myeloma cell lines (<5 μmol/L) and induced apoptosis. Sensitivity to GTx-134 correlated with IGF-1R signal inhibition. Expression of MDR-1 and CD45 were associated with resistance to GTx-134. Coculture with insulin-growth factor-1 (IGF-1) or adherence to bone marrow stroma conferred modest resistance, but did not overcome GTx-134-induced cytotoxicity. GTx-134 showed in vitro synergies when combined with dexamethasone or lenalidomide. Further, GTx-134 enhanced the activity of PD173074, a fibroblast growth factor receptor 3 (FGFR3) inhibitor, against t(4;14) myeloma cells. Therapeutic efficacy of GTx-134 was shown against primary cells and xenograft tumors. Although dysregulation of glucose homeostasis was observed in GTx-134-treated mice, impairment of glucose tolerance was modest. CONCLUSIONS: These studies support the potential therapeutic efficacy of GTx-134 in MM. Further, they provide a rationale for clinical application in combination with established antimyeloma treatments and novel targeted therapies.
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Authors | Sheng-Ben Liang, Xiu-Zhi Yang, Young Trieu, Zhihua Li, Jessica Zive, Chungyee Leung-Hagesteijn, Ellen Wei, Sergey Zozulya, Christopher C Coss, James T Dalton, Ivan George Fantus, Suzanne Trudel |
Journal | Clinical cancer research : an official journal of the American Association for Cancer Research
(Clin Cancer Res)
Vol. 17
Issue 14
Pg. 4693-704
(Jul 15 2011)
ISSN: 1557-3265 [Electronic] United States |
PMID | 21632854
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- GTx 134
- Heterocyclic Compounds, 3-Ring
- Sulfones
- Receptor, IGF Type 1
- Proto-Oncogene Proteins c-akt
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Topics |
- Animals
- Antineoplastic Agents
(chemistry, pharmacology, toxicity)
- Apoptosis
(drug effects)
- Cell Line, Tumor
- Cell Survival
(drug effects)
- Disease Models, Animal
- Drug Synergism
- Female
- Heterocyclic Compounds, 3-Ring
(chemistry, pharmacology, toxicity)
- Humans
- Mice
- Multiple Myeloma
(metabolism)
- Phosphorylation
(drug effects)
- Proto-Oncogene Proteins c-akt
(antagonists & inhibitors)
- Receptor, IGF Type 1
(antagonists & inhibitors)
- Signal Transduction
(drug effects)
- Stromal Cells
(drug effects, metabolism)
- Sulfones
(chemistry, pharmacology, toxicity)
- Tumor Burden
(drug effects)
- Xenograft Model Antitumor Assays
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