The Four-Herb Chinese Medicine PHY906 Reduces Chemotherapy-Induced Gastrointestinal Toxicity

被引:342
作者
Lam, Wing [1 ]
Bussom, Scott [1 ]
Guan, Fulan [1 ]
Jiang, Zaoli [1 ,2 ]
Zhang, Wei [1 ]
Gullen, Elizabeth A. [1 ]
Liu, Shwu-Huey [2 ]
Cheng, Yung-Chi [1 ]
机构
[1] Yale Univ, Sch Med, New Haven, CT 06520 USA
[2] PhytoCeutica Inc, New Haven, CT 06511 USA
关键词
HUMAN LIVER CARBOXYLESTERASE; INTESTINAL STEM-CELLS; NITRIC-OXIDE SYNTHASE; FACTOR-KAPPA-B; IRINOTECAN CPT-11; PROSTAGLANDIN E-2; SCUTELLARIA-BAICALENSIS; CANCER-THERAPY; INHIBITION; WOGONIN;
D O I
10.1126/scitranslmed.3001270
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
PHY906, a four-herb Chinese medicine formula first described 1800 years ago, decreases gastrointestinal toxicity induced by the chemotherapeutic drug CPT-11 ( irinotecan), as shown in a phase I/II clinical study. Similarly, in a murine colon 38 allograft model, PHY906 increased the antitumor activity of CPT-11 while decreasing animal weight loss caused by CPT-11. Here, we have further examined the effect of PHY906 on the intestinal toxicity caused by CPT-11 in mice. PHY906 did not protect against the initial DNA damage and apoptosis triggered by CPT-11 in the intestine, but by 4 days after CPT-11 treatment, PHY906 had restored the intestinal epithelium by promoting the regeneration of intestinal progenitor or stem cells and several Wnt signaling components. PHY906 also potentiated Wnt3a activity in human embryonic kidney-293 cells. Furthermore, PHY906 exhibited anti-inflammatory effects in mice by decreasing the infiltration of neutrophils or macrophages, tumor necrosis factor-alpha expression in the intestine, and pro-inflammatory cytokine concentrations in plasma. Chemical constituents of PHY906 potently inhibited nuclear factor kappa B, cyclooxygenase-2, and inducible nitric oxide synthase. Our results show that the herbal medicine PHY906 can counteract the toxicity of CPT-11 via several mechanisms that act simultaneously.
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页数:8
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