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Article

T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug

  • Authors:
    • Zhen Wang
    • Xing-Min Li
    • Kun Shang
    • Peng Zhang
    • Chao-Fu Wang
    • Yu-Hu Xin
    • Lu Zhou
    • Ying-Yi Li
  • View Affiliations / Copyright

    Affiliations: Cancer Research Institute, Fudan University Shanghai Cancer Center, Shanghai, P.R. China, Community Health Service Management Center, Yuhong District, Shengyang, Liaoning, P.R. China, Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, P.R. China
  • Pages: 1245-1251
    |
    Published online on: January 11, 2013
       https://doi.org/10.3892/or.2013.2233
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Abstract

Pim-3 kinase has been shown to be aberrantly expressed in premalignant and malignant lesions of endoderm-derived organs such as the liver, pancreas, colon and stomach. Pim-3 kinase inactivates the Bad protein, a proapoptotic molecule, and improves the expression of Bcl-xL, an antiapoptotic molecule, to promote cell proliferation. Thus, blocking Pim-3 kinase activity may be a new strategy for the treatment of pancreatic cancer. In this study, we screened low molecular compounds and observed that the stemonamide synthetic intermediate, T-18, potently inhibited Pim kinase activity. Moreover, T-18 inhibited the proliferation of human pancreatic, as well as that of hepatocellular and colon cancer cells in vitro. It also induced the apoptosis of human pancreatic carcinoma cells in vitro by decreasing the levels of phospho-Ser112-Bad; the levels of Pim-3 kinase and total Bad protein were not altered. Furthermore, T-18 inhibited the growth of human pancreatic cancer cells in nude mice without apparent adverse effects when the tumor was palpable. These observations indicate that stemonamide synthetic intermediates may be novel drugs for the treatment of gastrointestinal cancers, particularly pancreatic cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Wang Z, Li X, Shang K, Zhang P, Wang C, Xin Y, Zhou L and Li Y: T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug. Oncol Rep 29: 1245-1251, 2013.
APA
Wang, Z., Li, X., Shang, K., Zhang, P., Wang, C., Xin, Y. ... Li, Y. (2013). T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug. Oncology Reports, 29, 1245-1251. https://doi.org/10.3892/or.2013.2233
MLA
Wang, Z., Li, X., Shang, K., Zhang, P., Wang, C., Xin, Y., Zhou, L., Li, Y."T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug". Oncology Reports 29.3 (2013): 1245-1251.
Chicago
Wang, Z., Li, X., Shang, K., Zhang, P., Wang, C., Xin, Y., Zhou, L., Li, Y."T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug". Oncology Reports 29, no. 3 (2013): 1245-1251. https://doi.org/10.3892/or.2013.2233
Copy and paste a formatted citation
x
Spandidos Publications style
Wang Z, Li X, Shang K, Zhang P, Wang C, Xin Y, Zhou L and Li Y: T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug. Oncol Rep 29: 1245-1251, 2013.
APA
Wang, Z., Li, X., Shang, K., Zhang, P., Wang, C., Xin, Y. ... Li, Y. (2013). T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug. Oncology Reports, 29, 1245-1251. https://doi.org/10.3892/or.2013.2233
MLA
Wang, Z., Li, X., Shang, K., Zhang, P., Wang, C., Xin, Y., Zhou, L., Li, Y."T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug". Oncology Reports 29.3 (2013): 1245-1251.
Chicago
Wang, Z., Li, X., Shang, K., Zhang, P., Wang, C., Xin, Y., Zhou, L., Li, Y."T-18, a stemonamide synthetic intermediate inhibits Pim kinase activity and induces cell apoptosis, acting as a potent anticancer drug". Oncology Reports 29, no. 3 (2013): 1245-1251. https://doi.org/10.3892/or.2013.2233
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