4.7 Article

Systematic transcriptome analysis reveals molecular mechanisms and indications of bupleuri radix

期刊

FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.1010520

关键词

herbal medicine; transcriptome; gene signature; pathway enrichment analysis; drug repurposing; wound healing

资金

  1. Korea Institute of Oriental Medicine [KSN2023120]
  2. National Research Council of Science & Technology (NST), Republic of Korea [KSN2023120] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Pharmacogenomic analysis revealed the molecular mechanisms of action of the herbal medicine Bupleuri Radix (BR) in inhibiting cancer cell proliferation and inducing apoptosis. The study also showed enhanced cell adhesion and migration with BR treatment, indicating its potential therapeutic effects for skin disorders. In addition, BR demonstrated a wound-healing effect in skin and lung cells. The main active ingredients of BR exhibited anti-cancer effects, but further research is needed on the minor ingredients.
Pharmacogenomic analysis based on drug transcriptomic signatures is widely used to identify mechanisms of action and pharmacological indications. Despite accumulating reports on the efficacy of medicinal herbs, related transcriptome-level analyses are lacking. The aim of the present study was to elucidate the underlying molecular mechanisms of action of Bupleuri Radix (BR), a widely used herbal medicine, through a systematic transcriptomic analysis. We analyzed the drug-responsive transcriptome profiling of A549 lung cancer cell line after treating them with multiple doses of BR water (W-BR) and ethanol (E-BR) extracts and their phytochemicals. In vitro validation experiments were performed using both A549 and the immortalized human keratinocyte line HaCaT. Pathway enrichment analysis revealed the anti-cancer effects of BR treatment via inhibition of cell proliferation and induction of apoptosis. Enhanced cell adhesion and migration were observed with the W-BR but not with the E-BR. Comparison with a disease signature database validated an indication of the W-BR for skin disorders. Moreover, W-BR treatment showed the wound-healing effect in skin and lung cells. The main active ingredients of BR showed only the anti-cancer effect of the E-BR and not the wound healing effect of the W-BR, suggesting the need for research on minor ingredients of BR.

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