Reference - Detail
| RRC ID | 49630 |
|---|---|
| Author | Ibata M, Iwasaki J, Fujioka Y, Nakagawa K, Darmanin S, Onozawa M, Hashimoto D, Ohba Y, Hatakeyama S, Teshima T, Kondo T. |
| Title | Leukemogenic kinase FIP1L1-PDGFRA and a small ubiquitin-like modifier E3 ligase, PIAS1, form a positive cross-talk through their enzymatic activities. |
| Journal | Cancer Sci |
| Abstract |
Fusion tyrosine kinases play a crucial role in the development of hematological malignancies. FIP1L1-PDGFRA is a leukemogenic fusion kinase that causes chronic eosinophilic leukemia. As a constitutively active kinase, FIP1L1-PDGFRA stimulates downstream signaling molecules, leading to cellular proliferation and the generation of an anti-apoptotic state. Contribution of the N-terminal FIP1L1 portion is necessary for FIP1L1-PDGFRA to exert its full transforming activity, but the underlying mechanisms have not been fully characterized. We identified PIAS1 as a FIP1L1-PDGFRA association molecule by yeast two-hybrid screening. Our analyses indicate that the FIP1L1 portion of FIP1L1-PDGFRA is required for efficient association with PIAS1. As a consequence of the association, FIP1L1-PDGFRA phosphorylates PIAS1. Moreover, the kinase activity of FIP1L1-PDGFRA stabilizes PIAS1. Therefore, PIAS1 is one of the downstream targets of FIP1L1-PDGFRA. Moreover, we found that PIAS1, as a SUMO E3 ligase, sumoylates and stabilizes FIP1L1-PDGFRA. In addition, suppression of PIAS1 activity by a knockdown experiment resulted in destabilization of FIP1L1-PDGFRA. Therefore, FIP1L1-PDGFRA and PIAS1 form a positive cross-talk through their enzymatic activities. Suppression of sumoylation by ginkgolic acid, a small molecule compound inhibiting a SUMO E1-activating enzyme, also destabilizes FIP1L1-PDGFRA, and while the tyrosine kinase inhibitor imatinib suppresses FIP1L1-PDGFRA-dependent cell growth, ginkgolic acid or siRNA of PIAS1 has a synergistic effect with imatinib. In conclusion, our results suggest that sumoylation by PIAS1 is a potential target in the treatment of FIP1L1-PDGFRA-positive chronic eosinophilic leukemia. |
| Volume | 108(2) |
| Pages | 200-207 |
| Published | 2017-2-1 |
| DOI | 10.1111/cas.13129 |
| PMID | 27960034 |
| PMC | PMC5367148 |
| MeSH | Apoptosis Cell Nucleus / metabolism* HEK293 Cells Humans Hypereosinophilic Syndrome / drug therapy Hypereosinophilic Syndrome / metabolism Imatinib Mesylate / therapeutic use Immunoblotting Immunoprecipitation Oncogene Proteins, Fusion / chemistry Oncogene Proteins, Fusion / metabolism* Protein Inhibitors of Activated STAT / chemistry Protein Inhibitors of Activated STAT / metabolism* Protein Kinase Inhibitors / therapeutic use Protein-Tyrosine Kinases / metabolism Receptor, Platelet-Derived Growth Factor alpha / chemistry Receptor, Platelet-Derived Growth Factor alpha / metabolism* STAT1 Transcription Factor / chemistry STAT1 Transcription Factor / metabolism* Signal Transduction Sumoylation Transfection / methods mRNA Cleavage and Polyadenylation Factors / chemistry mRNA Cleavage and Polyadenylation Factors / metabolism* |
| IF | 4.966 |
| Times Cited | 1 |
| Altmetric score |
オルトメトリクス指標項目
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| The most frequently cited source | Wikipedia |
| Total number of mentions | 1 |
| Altmetric score changes over past 6months | 3.0 |
| Resource | |
| DNA material | pFLAG-FIP1L1-PDGFRA-FL (RDB15460) pFLAG-FIP1L1-PDGFRA-KD (RDB15461) pFLAG-PDGFRA-C (RDB15462) pCGT-FIP1L1-PDGFRA-FL (RDB15463) pCGT-FIP1L1-PDGFRA-KD (RDB15464) pCGT-PDGFRAC (RDB15465). |