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南瓜多糖通过抑制人肝癌 HepG2 细胞中的 JAK2/STAT3 通路诱导细胞凋亡。

A pumpkin polysaccharide induces apoptosis by inhibiting the JAK2/STAT3 pathway in human hepatoma HepG2 cells.

机构信息

Department of Medical Oncology, The 2nd affiliated Hospital of Harbin Medical University, Harbin 150086, China.

Department of Medical Oncology, Second Tumor Hospital of Heilongjiang Province, Harbin 150088, China.

出版信息

Int J Biol Macromol. 2017 Nov;104(Pt A):681-686. doi: 10.1016/j.ijbiomac.2017.06.078. Epub 2017 Jun 17.

Abstract

The purpose of this study is to investigate the effect of a purified polysaccharide (PPPF) from pumpkin fruit on the Janus activated kinase (JAK)/signal transducer and activator of transcription (STAT) signaling during apoptotic process. The results showed that PPPF or STAT3 siRNA inhibits the cell growth of HepG2 cells via induction of apoptosis. Moreover, PPPF is able to suppress both constitutive and IL-6-induced phosphorylation of STAT3 (on Tyr705) and subsequent nuclear translocation in cancer cells. Such inhibition is found to be achieved through down-regulation of constitutive phosphorylation of JAK2, but not JAk1, c-Src, ERK1/2, and Akt, which means STAT3 tyrosine phosphorylation in HepG2 cells following PPPF treatment is associated with a reduction in JAK2 activity. In addition, the protein expression of SHP-1 was increased in cells in response to PPPF treatment, whereas SHP-2, SOCS-1 and SCOS-3 protein expression remain unchanged. In vivo animal experiment also indicated that PPPF had a potent inhibitory effect on tumor growth in mice bearing HepG2 xenograft tumors. Thus we can conclude that PPPF directly induces apoptotic cell death of HepG2 cells via down-regulation of the JAK2/STAT3 signal transduction pathways, which may facilitates the development of a therapeutic strategy for treating HCC.

摘要

本研究旨在探讨南瓜果实中一种纯化多糖(PFFF)在凋亡过程中对 Janus 激活激酶(JAK)/信号转导和转录激活因子(STAT)信号的影响。结果表明,PFFF 或 STAT3 siRNA 通过诱导细胞凋亡抑制 HepG2 细胞的生长。此外,PFFF 能够抑制癌细胞中组成型和 IL-6 诱导的 STAT3(Tyr705 上)磷酸化以及随后的核易位。这种抑制作用是通过下调组成型磷酸化 JAK2 实现的,而不是 JAK1、c-Src、ERK1/2 和 Akt,这意味着 PPPF 处理后 HepG2 细胞中的 STAT3 酪氨酸磷酸化与 JAK2 活性的降低有关。此外,细胞对 PPPF 处理的反应中 SHP-1 的蛋白表达增加,而 SHP-2、SOCS-1 和 SCOS-3 蛋白表达保持不变。体内动物实验也表明,PFFF 对荷瘤小鼠的 HepG2 移植瘤生长具有很强的抑制作用。因此,我们可以得出结论,PFFF 通过下调 JAK2/STAT3 信号转导通路直接诱导 HepG2 细胞的凋亡性细胞死亡,这可能有助于开发治疗 HCC 的治疗策略。

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