PTEN is involved in Kanglaite® injection-induced apoptosis of human pancreatic cancer cells

被引:0
作者
Liu, Ying [1 ]
Sun, Xuejia [2 ]
Xiao, Yin [1 ]
Liu, Shi [3 ]
Zhao, Jing [3 ]
Qin, Wei [4 ]
机构
[1] Qiqihar Med Univ, Affiliated Hosp 3, Dept Oncol, 27 Taishun Rd, Qiqihar 161099, Heilongjiang, Peoples R China
[2] Qiqihar Med Univ, Affiliated Hosp 3, Dept Radiol, Qiqihar 161099, Heilongjiang, Peoples R China
[3] Qiqihar Med Univ, Affiliated Hosp 3, Dept Gen Surg, Qiqihar 161099, Heilongjiang, Peoples R China
[4] Qiqihar Med Univ, Qiqihar 161099, Heilongjiang, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2019年 / 12卷 / 02期
关键词
Coix; oncogene protein v-akt; pancreatic neoplasms; PTEN phosphohydrolase; TOR serine-threonine kinases; INHIBITION; EXPRESSION; MECHANISM; THERAPY; PATHWAY; KLT; AKT;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Kanglaite (R) injection (KLT) exhibits anti-cancer activities in a variety of cancers. The main ingredient is the traditional Chinese medicine Coix seed oil, which has been previously used in the adjunctive therapy of cancer in China. The PI3K/Akt/mTOR signaling pathway be able to progress cell survival and proliferation in various cancers. PTEN (Phosphatase and tensin homolog deleted on the chromosome 10) is a major inhibitory controller of the PI3K/Akt/mTOR signaling and a critical cancer-suppressor protein. In this study, we examined the mechanisms underlying the effects of KLT in pancreatic cancer cells and the potential role of PTEN. Methods: Flow cytometry and CCK-8 assay were used to examine apoptosis and proliferation, respectively, of PANC-1 cells. RT-PCR and western blotting were performed to measure the expression of genes and proteins, respectively, in the PI3K/Akt/mTOR signaling pathway. Results: KLT induced growth inhibition and apoptosis in pancreatic cancer cells, and these activities were weakened in PTEN-knockdown cells. KLT treatment also resulted in decreased levels of p-Akt and p-mTOR, along with enhanced PTEN. Conclusions: Our results revealed that KLT can induce apoptosis and suppress proliferation of pancreatic cancer cells through the induction of PTEN and downregulation of pAkt and p-mTOR and the PI3K/Akt/mTOR pathway. Our study shows that KLT could be a potential treatment strategy for pancreatic cancer that harbors functional PTEN.
引用
收藏
页码:1658 / 1665
页数:8
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