Unknown

Dataset Information

0

Probing Synergistic Targets by Natural Compounds for Hepatocellular Carcinoma.


ABSTRACT:

Background

Designing combination drugs for malignant cancers has been restricted due to the scarcity of synergy-medicated targets, while some natural compounds have demonstrated potential to enhance anticancer effects.

Methods

We here explored the feasibility of probing synergy-mediated targets by Berberine (BER) and Evodiamine (EVO) in hepatocellular carcinoma (HCC). Using the genomics-derived HCC signaling networks of compound treatment, NF-κB and c-JUN were inferred as key responding elements with transcriptional activity coinhibited during the synergistic cytotoxicity induction in BEL-7402 cells. Then, selective coinhibitors of NF-κB and c-JUN were tested demonstrating similar synergistic antiproliferation activity.

Results

Consistent with in vivo experiments of zebrafish, coinhibitors were found to significantly reduce tumor growth by 79% and metastasis by 96% compared to blank control, accompanied by anti-angiogenic activity. In an analysis of 365 HCC individuals, the low expression group showed significantly lower malignancies and better prognosis, with the median survival time increased from 67 to 213%, compared to the rest of the groups.

Conclusion

Together, NF-κB and c-JUN were identified as promising synergistic inducers in developing anti-HCC therapies. Also, our method may provide a feasible strategy to explore new targeting space from natural compounds, opening opportunities for the rational design of combinational formulations in combatting malignant cancers.

SUBMITTER: Gao J 

PROVIDER: S-EPMC8355820 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC7894118 | biostudies-literature
| S-EPMC7443834 | biostudies-literature
| S-EPMC8750630 | biostudies-literature
| S-EPMC8708931 | biostudies-literature
| S-EPMC8509806 | biostudies-literature
| S-EPMC5501181 | biostudies-literature
| S-EPMC8505848 | biostudies-literature
| S-EPMC5958667 | biostudies-literature
| S-EPMC4427038 | biostudies-literature
| S-EPMC9006883 | biostudies-literature