3.9 Article

Exposure of Hepatocellular Carcinoma Cells to Ankaferd Blood Stopper® Alters Cell Death Signaling Networks Confirmed by Oncoproteomic and Genomic Profiling Studies

Journal

CURRENT TRADITIONAL MEDICINE
Volume 7, Issue 2, Pages 223-235

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/2215083806666200117093815

Keywords

Hepatocellular carcinoma; Ankaferd (R); endoplasmic reticulumi; blood stopper; oncoproteomics and gene expression

Funding

  1. Scientific Research Projects Coordination Unit of Hacettepe University, Ankara - Turkey [17656]

Ask authors/readers for more resources

The commercially available herbal extract Ankaferd Blood Stopper was studied for its effects on HEPG2 hepatocellular carcinoma cells, revealing no significant inhibition of cell viability after 24 hours but a clear reduction after 72 hours. Genomic and oncoproteomic analysis showed diversification, with effects on protein processing networks and potential activation of the mitochondrial apoptotic pathway. Unlike many chemotherapeutic agents, Ankaferd did not induce drug resistance, indicating its potential for combination therapy against hepatocellular carcinoma.
Background: Ankaferd Blood Stopper (R) is a commercially available herbal extract with potent blood-stopping property and is clinically used to treat immediate dental, dermal, external and internal bleeding. Its possible anti-neoplastic effect or whether it ingenerates drug resistance in cells has not been previously scrutinized. Objective: In the present study, HEPG2 hepatocellular carcinoma cell line was exposed to clinically used dose (8 mu L/mL) of the blood stopper for 24 h and the behavioral changes were investigated on both proteomic and genomic levels. Methods: Cell culture experiments were performed by using Ankaferd (R) application in HEPG2 cell line. Cytotoxic activity experiments with MTT, oncoproteomic studies with 2- D gel electrophoresis, genomic studies were performed with RT-PCR. Results: It was seen that the agent did not significantly inhibit cell viability subsequent to 24 h of the treatment meanwhile, it clearly deducted cell viability after 72 h. Although reduction of HEPG2 cell proliferation was not witnessed as a response to 24 h of treatment with Ankaferd (R), genomic and oncoproteomic analysis demonstrated diversification. Conclusion: It was established that protein processing networks in endoplasmic reticulum which regulate protein folding, relocation and degradation were effected. Additionally, it was proved that along with the elongation of the exposure period, mitochondrial apoptotic pathway may be activated due to hnRNP F-p53 interaction. Given to the fact that the agent did not cause P-glycoprotein-dependent drug resistance unlike many clinically used chemotherapeutic agents, it can also be considered for combination treatment. Overall, these findings suggest that Ankaferd (R) offers a novel promising approach against hepatocellular carcinoma which needs further investigation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.9
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available