Zhang Xiao-Lan, Wang Bin-Bin, Mo Jian-Shu
Department of Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310006, P.R. China.
Department of Oncology, Cixi City Hospital of Traditional Chinese Medicine, Ningbo, Zhejiang 315300, P.R. China.
Oncol Lett. 2018 Nov;16(5):5557-5564. doi: 10.3892/ol.2018.9364. Epub 2018 Aug 24.
Puerarin 6″-O-xyloside (PRX) is a major compound found in the root of the (Willd.) Ohwi. The present study aimed to investigate the antitumor activity of PRX against colon cancer and examine its possible mechanism. In the present study, the anti-proliferative effects of PRX against colon cell lines (SW480, LoVo and HCT-116) were evaluated using a Cell Counting Kit-8 assay, and the half maximal inhibitory concentration values of the SW480, LoVo and HCT-11 cells were 37.114, 49.213 and 43.022 µg/ml, respectively. Furthermore, the apoptosis of SW480 cells was detected using flow cytometry with Annexin V-fluorescein isothiocyanate/propidium iodide staining. Subsequently, western blot analysis was performed to examine the expression of proteins associated with apoptosis, invasion and metastasis of tumors. The results showed that PRX possessed antitumor activity against colon cancer cell lines in a dose-dependent and time-dependent manner. In addition, PRX significantly upregulated the expression levels of cleaved (c)-caspase-3, c-caspase-9, B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein and phosphorylated c-Jun terminal kinase, and downregulated the expression levels of Bcl-2, matrix metalloproteinase (MMP)-3, MMP-9 and vascular endothelial growth factor (P<0.01). Therefore, the present study demonstrated the PRX exerted antitumor activity against colon cancer cell lines and that the anticancer mechanisms of PRX may be associated with the induction of mitochondria-mediated intrinsic apoptosis, and inhibition of tumor invasion and metastasis. The present study provides a scientific basis for the clinical use of PRX for the treatment of colon cancer.
葛根素6″-O-木糖苷(PRX)是野葛(Willd.)Ohwi根中发现的一种主要化合物。本研究旨在探讨PRX对结肠癌的抗肿瘤活性并研究其可能的作用机制。在本研究中,使用细胞计数试剂盒-8法评估PRX对结肠癌细胞系(SW480、LoVo和HCT-116)的抗增殖作用,SW480、LoVo和HCT-11细胞的半数最大抑制浓度值分别为37.114、49.213和43.022μg/ml。此外,采用膜联蛋白V-异硫氰酸荧光素/碘化丙啶染色的流式细胞术检测SW480细胞的凋亡情况。随后,进行蛋白质印迹分析以检测与肿瘤凋亡、侵袭和转移相关的蛋白质表达。结果表明,PRX对结肠癌细胞系具有剂量和时间依赖性的抗肿瘤活性。此外,PRX显著上调了裂解型(c)-半胱天冬酶-3、c-半胱天冬酶-9、B细胞淋巴瘤2(Bcl-2)、Bcl-2相关X蛋白和磷酸化c-Jun末端激酶的表达水平,并下调了Bcl-2、基质金属蛋白酶(MMP)-3、MMP-9和血管内皮生长因子的表达水平(P<0.01)。因此,本研究表明PRX对结肠癌细胞系具有抗肿瘤活性,且PRX的抗癌机制可能与诱导线粒体介导的内源性凋亡以及抑制肿瘤侵袭和转移有关。本研究为PRX临床治疗结肠癌提供了科学依据。