4.6 Article

Engagement of DYRK2 in proper control for cell division

期刊

CELL CYCLE
卷 14, 期 6, 页码 802-807

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/15384101.2015.1007751

关键词

apoptosis; cell cycle regulation; DYRK2; EMT; proteasomal degradation

资金

  1. Japan Society for the Promotion of Science
  2. Jikei University Graduate Research Fund
  3. Uehara Memorial Foundation
  4. Nakajima Foundation
  5. Sagawa Foundation for Promotion of Cancer Research
  6. Japan Foundation for Applied Enzymology
  7. Project Mirai Cancer Research Grants
  8. Vehicle Racing Commemorative Foundation
  9. Grants-in-Aid for Scientific Research [26830083] Funding Source: KAKEN

向作者/读者索取更多资源

Dysregulation of cell cycle machinery causes abnormal cell division, leading to cancer development. To drive cell cycle properly, expression levels of cell cycle regulators are tightly regulated through the cell cycle. Dual specificity tyrosine phosphorylation-regulated kinase 2 (DYRK2) is a Ser/Thr kinase, and its intracellular functions had not been elucidated for decades. Recent studies have shown that DYRK2 down-regulates key molecules on cell cycle control. This review mainly highlights the DYRK2 function during cell division. In addition, we summarize tumor suppressive role of DYRK2 in cancer cells and discuss future research directions for DYRK2 toward the novel cancer therapies.

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