Evidence map›Paper›PMID 33436534›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2021

Systems Pharmacology-Based Identification of Mechanisms of Action of Bolbostemma paniculatum for the Treatment of Hepatocellular Carcinoma.

Lan-Lan Wang, Chen Liao, Xiao-Qiang Li, Rong Dai, Qing-Wei Ren, Hai-Long Shi, Xiao-Ping Wang, Xue-Song Feng, Xu Chao

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Lan-Lan WangCollege of Basic Medicine, Shaanxi University of Chinese Medicine, Xi'an, Shaanxi, China (mainland).
Chen LiaoDepartment of Pharmacology, Yunnan University of Chinese Medicine, Kunming, Yunnan, China (mainland).
Xiao-Qiang LiKey Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Rong DaiDepartment of Pharmacology, Yunnan University of Chinese Medicine, Kunming, Yunnan, China (mainland).
Qing-Wei RenThe Second Affiliated Hospital of Shaanxi University of Chinese Medicine, Xi'an, Shaanxi, China (mainland).
Hai-Long ShiCollege of Basic Medicine, Shaanxi University of Chinese Medicine, Xi'an, Shaanxi, China (mainland).
Xiao-Ping WangCollege of Basic Medicine, Shaanxi University of Chinese Medicine, Xi'an, Shaanxi, China (mainland).
Xue-Song FengCollege of Basic Medicine, Shaanxi University of Chinese Medicine, Xi'an, Shaanxi, China (mainland).
Xu ChaoCollege of Basic Medicine, Shaanxi University of Chinese Medicine, Xi'an, Shaanxi, China (mainland).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Traditional Chinese medicine has widely used Bolbostemma paniculatum to treat diseases, including cancer, but its underlying mechanisms remain unclear. The present study aimed to elucidate the potential pharmacological mechanisms of "Tu Bei Mu" (TBM), the Chinese name for Bolbostemmatis Rhizoma, the dry tuber of B. paniculatum, for the treatment of hepatocellular carcinoma (HCC). MATERIAL AND METHODS The active components and putative therapeutic targets of TBM were explored using SwissTargetPrediction, Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP), and Search Tool for Interactions of Chemicals (STITCH). The HCC-related target database was built using DrugBank, DisGeNet, Online Mendelian Inheritance in Man (OMIM), and Therapeutic Target Database (TTD). A protein-protein interaction network of the common targets was constructed, based on the matches between TBM potential targets and HCC-related targets, using Cytoscape software. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses of the cluster networks were used to elucidate the biological functions of TBM. RESULTS Pharmacological network diagrams of the TBM compound-target network and HCC-related target network were successfully constructed. A total of 22 active components, 191 predicted biological targets of TBM, and 3775 HCC-related targets were identified. Through construction of an HCC-related target database and a protein-protein interaction network of the common targets, TBM was predicted to be effective in treating HCC mainly through the PI3K-Akt, HIF-1, p53, and PPAR signaling pathways. CONCLUSIONS The PI3K/Akt, HIF1, p53, and PPAR pathways may play vital roles in TBM treatment of HCC. Also, the potential anti-cancer effect of TBM on HCC appears to stem from the synergetic effect of multiple targets and mechanisms.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularDatabases, ChemicalDatabases, GeneticDrugs, Chinese HerbalHumansLiver NeoplasmsProtein Interaction MapsSignal TransductionSystems BiologyAntineoplastic AgentsDrugs, Chinese Herbal

Identifiers

PMID33436534
PMCPMC7812697

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.