Evidence map›Paper›PMID 34311656›Full record

ArticleBioengineered2021

Anti-neoplastic characteristics and potential targets of calycosin against bisphenol A-related osteosarcoma: bioinformatics analysis.

Qijin Pan, Ka Wu, Jiachang Tan, Yu Li, Xiao Liang, Min Su

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Bioinformatics andFrontiers in endocrinology · 2022
    Article
  5. Article
  6. Review
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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

6 authors at 3 institutions in 1 country.

Qijin PanDepartment of Oncology, Guigang City Peoples' Hospital, The Eighth Affiliated Hospital of Guangxi Medical University, Guigang, Guangxi, PR China.
Ka WuDepartment of Pharmacy, The Second People's Hospital of Nanning City, the Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jiachang TanDepartment of Bone and Soft Tissue Surgery, Affiliated Tumor Hospital, Guangxi Medical University, Nanning, PR China.
Yu LiLaboratory of Environmental Pollution and Integrative Omics, Guilin Medical University, Guilin, PR China.
Xiao LiangLaboratory of Environmental Pollution and Integrative Omics, Guilin Medical University, Guilin, PR China.
Min SuLaboratory of Environmental Pollution and Integrative Omics, Guilin Medical University, Guilin, PR China.ORCID 0000-0002-7867-1539
Guilin Medical University · CNGuangxi Medical University · CNTumor Hospital of Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Environmentally, bisphenol A (BPA) is a well-known pollutant caused human health risk, including osteosarcoma (OS). OS, a deadly bone neoplasia, may occur in children and adults. However, the anti-OS pharmacotherapy prescribes limitedly in clinical practice. Interestingly, previous experimental evidences indicate calycosin-exerting potential anti-OS actions. Thus, in this report, we aimed to further characterize and detail the therapeutic targets and molecular mechanisms of calycosin-anti-BPA-related OS by using network pharmacology and molecular docking analyses. In results, the bioinformatics data disclosed all mapped, core targets, biological functions, molecular pathways of calycosin to treat BPA-related OS. The computational analysis using molecular docking indicated that potential binding ability of core targets in calycosin to treat BPA-related OS was identified. Moreover, detailed biological functions and optimal pathways of calycosin-anti-BPA-related OS were revealed, as shown in integrated network maps. Taken together, these network pharmacology and structural biology findings illustrate the core biotargets, pharmacological functions and pathways of calycosin-anti-BPA-related OS. Potentially, these core targets identified by molecular docking may attribute to the potential clinical application of calycosin against BPA-related OS.[Formula: see text].

Indexed as

Antineoplastic AgentsIsoflavonesBenzhydryl CompoundsBisphenol A CompoundsBone NeoplasmsComputational BiologyGene Expression Regulation, NeoplasticHumansMolecular Docking SimulationOsteosarcomaPhenols7,3'-dihydroxy-4'-methoxyisoflavoneAntineoplastic AgentsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsIsoflavonesPhenolsBisphenol Acalycosinfindingsmolecular dockingnetwork pharmacologyOsteosarcoma

Identifiers

PMID34311656
PMCPMC8806932
OpenAlexW3185317324

What OpenQuestion holds

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Read underepoch 390

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 OpenQuestion graph.