ReferenceID 4130

Chinese Dragon's Blood EtOAc Extract Inhibits Liver Cancer Growth Through Downregulation of Smad3

Front Pharmacol

Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies, which ranks the third leading cause of cancer-related death worldwide. The screening of anti-HCC drug with high efficiency and low toxicity from t

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Reference Id
4130
Evidence Id
20720
Core Evidence Id
20720
Source Reference Id
1536
Herb2 Reference Id
HBREF002333
Subject Paper Key
HERB002817_32477135
Pubmed Id
32477135
Doi
10.3389/fphar.2020.00669
Paper Title
Chinese Dragon's Blood EtOAc Extract Inhibits Liver Cancer Growth Through Downregulation of Smad3
Paper Abstract
Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies, which ranks the third leading cause of cancer-related death worldwide. The screening of anti-HCC drug with high efficiency and low toxicity from traditional Chinese medicine (TCM) has attracted more and more attention. As a TCM, Chinese dragon's blood has been used for the treatment of cardiovascular illness, gynecological illness, skin disorder, otorhinolaryngological illness, and diabetes mellitus complications for many years. However, the anti-tumor effect and underlying mechanisms of Chinese dragon's blood remain ill-defined. Herein we have revealed that Chinese dragon's blood EtOAc extract (CDBEE) obviously suppressed the growth of human hepatoma HepG2 and SK-HEP-1 cells. Moreover, CDBEE inhibited the migration and invasion of HepG2 and SK-HEP-1 cells. Additionally, CDBEE displayed good in vitro anti-angiogenic activity. Importantly, CDBEE treatment significantly blunted the oncogenic capability of HepG2 cells in nude mice. Mechanistically, CDBEE inhibited Smad3 expression in human hepatoma cells and tumor tissues from nude mice. Using RNA interference, we demonstrated that CDBEE exerted anti-hepatoma activity partially through down-regulation of Smad3, one of major members in TGF-beta/Smad signaling pathway. Therefore, CDBEE may be a promising candidate drug for HCC treatment, especially for liver cancer with aberrant TGF-beta/Smad signaling pathway.
Journal
Front Pharmacol
Publish Year
2020
Experiment Subject
mouse; human; hepg2; hepg2 cells; human hepatoma hepg2; sk-hep-1 cells
Experiment Type
Animal & Cell Experiment
Phenotype Related
Hepatoma; Cancer-related Death; Malignancies; Tumor; Cardiovascular Illness; Liver Cancer; Gynecological Illness; Diabetes Mellitus; Skin Disorder; Otorhinolaryngological Illness; Hepatocellular Carcinoma
Paper Title Cn
Paper Title En
Chinese Dragon's Blood EtOAc Extract Inhibits Liver Cancer Growth Through Downregulation of Smad3
Bilingual Status
semi_complete