Evidence map›Paper›PMID 35770417›Full record

ArticleCombinatorial chemistry & high throughput screening2025

Mitigation of QingLuoTongMai Pills on Chemotherapy-induced Phlebitis: A Network Pharmacology Study and Experimental Validation.

Ning Yu, Shi-Kai Zhang, Jian Chen, Cheng Zhao, Ye-Min Cao, Ling Li, Yong-Bing Cao

Abstract read
PubMed Publisher
In one paragraph

Article in Combinatorial chemistry & high throughput screening, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

7 authors at 4 institutions in 2 countries.

Ning YuShanghai University of Traditional Chinese Medicine, Shanghai, China.
Shi-Kai ZhangInstitute of Vascular Disease, Shanghai University of TCM Shanghai TCM-Integrated Hospital, Shanghai, China.
Jian ChenInstitute of Vascular Disease, Shanghai University of TCM Shanghai TCM-Integrated Hospital, Shanghai, China.
Cheng ZhaoShanghai Traditional Chinese Medicine Integrated Institute of Vascular Department, Shanghai, China.
Ye-Min CaoShanghai Traditional Chinese Medicine Integrated Institute of Vascular Department, Shanghai, China.
Ling LiInstitute of Vascular Disease, Shanghai University of TCM Shanghai TCM-Integrated Hospital, Shanghai, China.
Yong-Bing CaoInstitute of Vascular Disease, Shanghai University of TCM Shanghai TCM-Integrated Hospital, Shanghai, China.
Shanghai University of Traditional Chinese Medicine · CNShanghai University · CNCM Hospital · KRShanghai Traditional Chinese Medicine Hospital · CN

Funding

National Natural Science Foundation of China 2018ZX09201008-002-091, 2018ZX09201008-002-092, 82104873Science and Technology Commission of Shanghai Municipality 19401901400Science and Technology Commission of Shanghai Municipality 19ZR1451800, 21ZR1460400Scientific Research Project of Traditional Chinese Medicine of Hongkou District Health HKQ-ZYY-2020-19Shanghai Sailing Program 20YF1445900Special Clinical Research Project of Health Profession of Shanghai Municipal Commission of Health 20194Y0081Xinglin Young Talent training Program of Shanghai University of Traditional Chinese Medicine RCPY0040
6 · The paper itself

Abstract

objectiveChemotherapy-induced phlebitis (CIP) is a side product of chemotherapy treatment for malignant tumors, which affects the therapeutic effect and quality of life of cancer patients, and still lacks a clear therapeutic means. In this study, we investigated the therapeutic effects of QLTMP on CIP using network pharmacology and verified the anti-inflammatory mechanism of QLTMP in a mice model induced by vinorelbine.

methodsNetwork pharmacology analysis was performed to identify bioactive compounds in QLTMP. The protein-protein interaction network was used to identify the core therapeutic targets of QLTMP against CIP, analyze biological function and pathway enrichment based on the identified core therapeutic targets, and evaluate the therapeutic effect of QLTMP in a model of CIP induced by vinorelbine to confirm the reliability of the network pharmacological analysis. One hundred and sixty-five bioactive compounds of QLTMP matched the screening criteria and identified 19 core therapeutic targets of QLTMP against CIP. Biofunctional analysis showed that the therapeutic effect of QLTMP on CIP was mainly related to the inhibition of inflammation, while pathway enrichment analysis showed that the TNF signaling pathway was involved in the inflammatory process.

resultsExperimental confirmation in a mice model showed that QLTMP exerts anti-inflammatory effects through modulation of the PI3K/AKT/TNF signaling pathway, a discovery consistent with the network pharmacological analysis. DISCUSSION AND

conclusionThe network pharmacological analysis of the anti-inflammatory mechanism of QLTMP on CIP and its exploration of

Indexed as

Anti-Inflammatory AgentsAntineoplastic AgentsDrugs, Chinese HerbalNetwork PharmacologyPhlebitisAnimalsDisease Models, AnimalHumansMiceMice, Inbred BALB CProtein Interaction MapsVinorelbineAnti-Inflammatory AgentsAntineoplastic AgentsDrugs, Chinese HerbalVinorelbinebioactive compounds.Chemotherapeutic phlebitischemotherapymitigationnetwork pharmacologytraditional Chinese medicine

Identifiers

PMID35770417
OpenAlexW4283755335

What OpenQuestion holds

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Registered trials

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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.