Evidence map›Paper›PMID 39398618›Full record

ArticleAmerican journal of translational research2024

Identification of molecular targets and underlying mechanisms of Fuzheng Shengbai Decoction against colon cancer based on network pharmacology.

Yu Wang, Shuiming Wang, Min Li, Qijia Zhang, Mingzhi Fang, Qin Zheng

Abstract read
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Article in American journal of translational research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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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

6 authors.

Yu WangDepartment of Oncology, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine Nanjing 210022, Jiangsu, China.
Shuiming WangDepartment of Proctology, Nanjing Hospital of Traditional Chinese Medicine Nanjing 210022, Jiangsu, China.
Min LiDepartment of Oncology, Nanjing Hospital of Traditional Chinese Medicine Nanjing 210022, Jiangsu, China.
Qijia ZhangDepartment of Oncology, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.
Mingzhi FangDepartment of Oncology, Nanjing Hospital of Traditional Chinese Medicine Nanjing 210022, Jiangsu, China.
Qin ZhengDepartment of Oncology, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine Nanjing 210003, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the molecular targets and underlying mechanisms of Fuzheng Shengbai Decoction (FZSBD) against colon cancer (CC).

methodsMultiple network pharmacology approaches were used to predict the molecular targets and underlying mechanisms of FZSBD against CC. The expression of potential molecular targets was determined. The effects of FZSBD on cell viability, proliferation, migration, invasion, and the cell cycle of CC cells were investigated. The therapeutic efficacy, hematological, immunological, and inflammatory data in patients with CC were evaluated after treatment with the XELOX regimen with and without FZSBD.

resultsA total of 912 potential targets in FZSBD and 2765 DEGs in CC specimens were screened. Five hub genes (TP53, MYC, VEGFA, CCND1, and IL1B) closely associated with immune-related signaling pathways and the cell cycle process were identified. The five hub genes were of prognostic value in CC. The gene and protein expression of the five hub genes was significantly higher in CC tumor tissue samples than that of normal tissue samples. Furthermore, with increasing doses, FZSBD increasingly inhibited growth, migration, and invasion, and suppressed the cell cycle process of CC cells. Supplementing of FZSBD to the XELOX regimen enhanced immune modulation and alleviated inflammatory responses.

conclusionsThis study identified the molecular targets and underlying mechanisms of FZSBD treatment against CC and may provide clues for future research on the treatment of CC with FZSBD.

Indexed as

colon cancerFuzheng Shengbai Decoctioninflammatory responsenetwork pharmacology

Identifiers

PMID39398618
PMCPMC11470291

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