Sericultural Research Institute, Zhejiang Academy of Agricultural Science, Hangzhou 310021, China.
Int J Biol Macromol. 2011 Apr 1;48(3):511-7. doi: 10.1016/j.ijbiomac.2011.01.014. Epub 2011 Jan 22.
Proteoglycan (P1) purified from Phellinus linteus has been reported to have anti-disease activities. The objectives of our research were to determine the anti-tumor effect and possible mechanisms of P1 on human cancer cells. Cell inhibition assay showed that P1 has an antiproliferative effect on HepG2, HT-29, NCI-H 460 and MCF-7 human colon cancer cells, especially it was very effective in inhibiting HT-29 cells. When HT-29-bearing mice were treated with P1(100mg/kg), there was relative increase in spleen and thymus weights, the plasmatic pIgR and IgA levels were significantly increased, also there was a notable decrease in plasmatic PGE2, Reg IV, EGFR and Akt concentrations measured by ELISA. RT-PCR analysis suggested that P1-induced HT-29 apoptosis appeared to be associated with a decrease in the levels of expression of Reg IV and EGFR. These results suggest that P1 might have two potential roles in treating cancer; it acts as an immunopotentiator partly through protecting T cells from escaping PGE2 attack and enhancing the mucosal IgA response, and as a direct inhibitor by disrupting the Reg IV/EGFR/Akt signaling pathway.
从木蹄层孔菌中提取的蛋白聚糖(P1)已被报道具有抗疾病活性。我们的研究目的是确定 P1 对人类癌细胞的抗肿瘤作用及其可能的机制。细胞抑制试验表明,P1 对 HepG2、HT-29、NCI-H460 和 MCF-7 人结肠癌细胞具有增殖抑制作用,特别是对 HT-29 细胞的抑制作用非常显著。当荷瘤 HT-29 小鼠用 P1(100mg/kg)治疗时,脾脏和胸腺重量相对增加,血浆 pIgR 和 IgA 水平显著升高,ELISA 检测到血浆 PGE2、RegIV、EGFR 和 Akt 浓度也明显降低。RT-PCR 分析表明,P1 诱导的 HT-29 细胞凋亡似乎与 RegIV 和 EGFR 表达水平的降低有关。这些结果表明,P1 可能在治疗癌症方面具有两个潜在作用;它作为一种免疫增强剂,部分通过保护 T 细胞免受 PGE2 攻击并增强黏膜 IgA 反应,以及通过破坏 RegIV/EGFR/Akt 信号通路作为直接抑制剂。