Evidence map›Paper›PMID 36451247›Full record

ArticleHereditas2022

Identification of GINS1 as a therapeutic target in the cancer patients infected with COVID-19: a bioinformatics and system biology approach.

Changpeng Hu, Yue Dai, Huyue Zhou, Jing Zhang, Dandan Xie, Rufu Xu, Mengmeng Yang, Rong Zhang

Open access · goldAbstract read
In one paragraph

Article in Hereditas, 2022. 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
0.4field-weighted citation impact, top 36% 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, 4 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

8 authors at 1 institution in 1 country.

Changpeng Hu *Department of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China.
Yue Dai *Department of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China.
Huyue ZhouDepartment of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China.
Jing ZhangDepartment of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China.
Dandan XieDepartment of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China.
Rufu XuDepartment of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China.
Mengmeng YangDepartment of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China. ymengmeng1980@163.com.
Rong ZhangDepartment of Pharmacy, The Second Affiliated Hospital of Army Medical University, 83 Xinqiao Road, 400037, Chongqing, China. xqpharmacylab@126.com.
Army Medical University · CN

Funding

the National Natural Science Foundation of China 81874357
6 · The paper itself

Abstract

backgroundCoronavirus disease 2019 (COVID-19) caused a series of biological changes in cancer patients which have rendered the original treatment ineffective and increased the difficulty of clinical treatment. However, the clinical treatment for cancer patients infected with COVID-19 is currently unavailable. Since bioinformatics is an effective method to understand undiscovered biological functions, pharmacological targets, and therapeutic mechanisms. The aim of this study was to investigate the influence of COVID-19 infection in cancer patients and to search the potential treatments.

methodsFirstly, we obtained the COVID-19-associated genes from seven databases and analyzed the cancer pathogenic genes from Gene Expression Omnibus (GEO) databases, respectively. The Cancer/COVID-19-associated genes were shown by Venn analyses. Moreover, we demonstrated the signaling pathways and biological functions of pathogenic genes in Cancer/COVID-19.

resultsWe identified that Go-Ichi-Ni-San complex subunit 1 (GINS1) is the potential therapeutic target in Cancer/COVID-19 by GEPIA. The high expression of GINS1 was not only promoting the development of cancers but also affecting their prognosis. Furthermore, eight potential compounds of Cancer/COVID-19 were identified from CMap and molecular docking analysis.

conclusionWe revealed the GINS1 is a potential therapeutic target in cancer patients infected with COVID-19 for the first time, as COVID-19 will be a severe and prolonged pandemic. However, the findings have not been verified actually cancer patients infected with COVID-19, and further studies are needed to demonstrate the functions of GINS1 and the clinical treatment of the compounds.

Indexed as

COVID-19NeoplasmsComputational BiologyDNA-Binding ProteinsHumansMolecular Docking SimulationPandemicsDNA-Binding ProteinsGINS1 protein, humanBioinformatics analysesCancer patientsCOVID-19GINS1Prognosis

Identifiers

PMID36451247
PMCPMC9713126
OpenAlexW4310496841

What OpenQuestion holds

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LicenceCC BY
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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.