Evidence map›Paper›PMID 38504574›Full record

ArticleCombinatorial chemistry & high throughput screening2024

The Role of Emodin in the Treatment of Bladder Cancer Based on Network Pharmacology and Experimental Verification.

Fule Liu, Jianghao Li, Boruo Zhou, Yang Shen, Jingyuan Tang, Jie Han, Changpeng Chen, Kang Shao, Haojie Chen, Lin Yuan

Abstract read
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In one paragraph

Article in Combinatorial chemistry & high throughput screening, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 25% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 1 country.

Fule LiuThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Jianghao LiThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Boruo ZhouThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Yang ShenDepartment of Urology, The Second Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Second Chinese Medicine Hospital, Jiangsu, 210017, China.
Jingyuan TangDepartment of Urology, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, 210004, China.
Jie HanDepartment of Urology, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, 210004, China.
Changpeng ChenDepartment of Urology, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, 210004, China.
Kang ShaoThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Haojie ChenThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Lin YuanDepartment of Urology, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, 210004, China.
Jiangsu Province Hospital · CNNanjing University of Chinese Medicine · CN58.com (China) · CN

Funding

Affiliated Hospital of Nanjing University of Chinese Medicine Foundation, China Y2022ZR25Jiangsu Commission of Health Foundation H2023130
6 · The paper itself

Abstract

background and purposeEmodin, a compound derived from rhubarb and various traditional Chinese medicines, exhibits a range of pharmacological actions, including antiinflammatory, antiviral, and anticancer properties. Nevertheless, its pharmacological impact on bladder cancer (BLCA) and the underlying mechanism are still unclear. This research aimed to analyze the pharmacological mechanisms of Emodin against BLCA using network pharmacology analysis and experimental verification.

methodsInitially, network pharmacology was employed to identify core targets and associated pathways affected by Emodin in bladder cancer. Subsequently, the expression of key targets in normal bladder tissues and BLCA tissues was assessed by searching the GEPIA and HPA databases. The binding energy between Emodin and key targets was predicted using molecular docking. Furthermore,

resultsOur analysis identified 148 common genes targeted by Emodin and BLCA, with the top ten target genes including

conclusionThis study integrates network pharmacology with

Indexed as

Cell ProliferationEmodinMolecular Docking SimulationNetwork PharmacologyUrinary Bladder NeoplasmsAntineoplastic AgentsAntineoplastic Agents, PhytogenicApoptosisCell Line, TumorCell MovementDrug Screening Assays, AntitumorHumansAntineoplastic AgentsAntineoplastic Agents, PhytogenicEmodinBladder canceremodinexperimental verification.molecular dockingmolecular mechanismnetwork pharmacology

Identifiers

PMID38504574
OpenAlexW4393010813

What Socratic holds

Textmetadata
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Registered trials

None linked

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 Socratic graph.