Diterpenoids from Scutellaria barbata D. Don Exert the Antiproliferative Effect on Colorectal Cancer Cells Via Hedgehog Signaling Pathway

被引:0
作者
Wang, Wenwen [1 ,3 ]
Tao, Zhongyi [1 ,3 ]
Tu, Linglan [1 ,3 ]
Huang, Wenkang [1 ,3 ]
Ye, Yiping [1 ,3 ]
Gao, Lijuan [1 ,3 ]
Li, Xiaoyu [1 ,2 ,3 ,4 ]
机构
[1] Hangzhou Med Coll, Sch Pharm, Hangzhou, Zhejiang, Peoples R China
[2] First Peoples Hosp Xiaoshan Dist, Dept Pathol, Hangzhou, Zhejiang, Peoples R China
[3] Hangzhou Med Coll, Sch Pharm, Key Lab Neuropsychiat Drug Res Zhejiang Prov, Hangzhou, Zhejiang, Peoples R China
[4] Hangzhou Med Coll, Sch Pharm, Hangzhou 310013, Zhejiang, Peoples R China
关键词
Scutellaria barbata D. Don; diterpenoids; colorectal cancer; Hedgehog pathway; SHH; NEOCLERODANE DITERPENOIDS; COLON-CANCER; CHLOROFORM FRACTION; ALKALOIDS; APOPTOSIS; GROWTH; PROLIFERATION; SUPPRESSION; INDUCTION; PROMOTES;
D O I
10.1177/09731296241234714
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Scutellaria barbata D. Don, also known as "Banzhilian" in China, the diterpenes of Banzhilian (Bzl-D) is a commonly used herbal medicine for treating various tumors including colorectal cancer (CRC). Objectives: This study aimed to examine the function of Bzl-D in inhibiting CRC development and explore its potential targets and mechanisms involving the Hedgehog (HH) pathway. Materials and methods: To determine the major components in Bzl-D, we performed ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-qTOF-MS) analysis. The proliferation, migration, invasion, and apoptosis abilities of the CRC HT-29 cell line were examined, and the related protein expression was tested. Tumorigenesis after treatment was detected by in vivo experiments. Results: Nineteen diterpenoids were detected, Bzl-D significantly inhibited the cell proliferation and metastasis and induced the apoptosis of HT-29 cells through binding to Sonic HH (SHH) and down-regulating the key proteins (SHH, patched, smoothened, and glioma-associated oncogene) of the HH pathway, thus. Of note, Bzl-D remarkably suppressed the growth of HT-29 xenografts in nude mice. Conclusion: This research demonstrates that Bzl-D is a promising anti-rectal cancer drug, providing a new entry point for targeted therapy of CRC.
引用
收藏
页码:877 / 886
页数:10
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