4.6 Review

Targeting Never-In-Mitosis-A Related Kinase 5 in Cancer: A Review

期刊

CURRENT MEDICINAL CHEMISTRY
卷 28, 期 30, 页码 6096-6109

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/0929867328666210322101749

关键词

Never-in-mitosis kinase family; mitosis; NEK5; therapeutic target; breast cancer; metastasis

资金

  1. Krewe de Pink, the local breast cancer survivor community organization
  2. Tulane Cancer Center
  3. AbbVie
  4. Bayer Pharma AG
  5. Boehringer Ingelheim
  6. Canada Foundation for Innovation
  7. Eshelman Institute for Innovation
  8. Genome Canada
  9. Innovative Medicines Initiative (EU/EFPIA)
  10. Janssen
  11. Merck KGaA Darmstadt Germany
  12. MSD
  13. Novartis Pharma AG
  14. Ontario Ministry of Economic Development and Innovation
  15. Pfizer
  16. Takeda
  17. Wellcome

向作者/读者索取更多资源

NEK5, an understudied member of the NEK family, is emerging as a key player in various solid tumors. Although there are currently no selective NEK5-targeting agents to test the effects of pharmacologic inhibition on cancer, recent advancements in this area are promising.
Mitotic kinases have integral roles in cell processes responsible for cancer development and progression in all tumor types and are common targets for therapeutics. However, a large subset of the human kinome remains unexplored with respect to functionality in cancer systems. Within the mitotic kinases, the never-in-mitosis kinase (NEK) family is emerging as novel kinase targets in various cancer types. NEK5 is an understudied member of the NEK family. While there are more recent studies describing the physiologic function of NEK5, its role in cancer biology remains widely understudied. However, emerging studies implicate that NEK5 has potentially crucial functions in various solid tumors. In this review, we discuss current knowledge regarding the role of NEK5 in cancer and the implications of NEK5 expression and activity in tumor development and metastasis. We summarize current studies that examine NEK5 activity in diverse cancer systems and cellular processes. As an understudied kinase, there are currently no selective NEK5-targeting agents to test the effects of pharmacologic inhibition on cancer, although there exist recent advancements in this area. Here we also include an update on efforts to develop selective pharmacologic inhibition of NEK5, and we discuss the current direction of NEK5-targeting therapeutic development. The generation of selective NEK5 inhibitors is promising new targeted therapies for cancer growth and metastasis.

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