Evidence map›Paper›PMID 33794574›Full record

ArticleRadiation oncology journal2021

Exploring the differentially expressed genes in human lymphocytes upon response to ionizing radiation: a network biology approach.

Tamizh Selvan Gnana Sekaran, Vishakh R Kedilaya, Suchetha N Kumari, Praveenkumar Shetty, Pavan Gollapalli

Open access · diamondAbstract read
In one paragraph

Article in Radiation oncology journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Tamizh Selvan Gnana SekaranCentral Research Laboratory, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangalore, India.
Vishakh R KedilayaCentral Research Laboratory, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangalore, India.
Suchetha N KumariCentral Research Laboratory, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangalore, India.
Praveenkumar ShettyCentral Research Laboratory, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangalore, India.
Pavan GollapalliCentral Research Laboratory, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangalore, India.
K S Hegde Medical Academy · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe integration of large-scale gene data and their functional analysis needs the effective application of various computational tools. Here we attempted to unravel the biological processes and cellular pathways in response to ionizing radiation using a systems biology approach. MATERIALS AND

methodsAnalysis of gene ontology shows that 80, 42, 25, and 35 genes have roles in the biological process, molecular function, the cellular process, and immune system pathways, respectively. Therefore, our study emphasizes gene/protein network analysis on various differentially expressed genes (DEGs) to reveal the interactions between those proteins and their functional contribution upon radiation exposure.

resultsA gene/protein interaction network was constructed, which comprises 79 interactors with 718 interactions and TP53, MAPK8, MAPK1, CASP3, MAPK14, ATM, NOTCH1, VEGFA, SIRT1, and PRKDC are the top 10 proteins in the network with high betweenness centrality values. Further, molecular complex detection was used to cluster these associated partners in the network, which produced three effective clusters based on the Molecular Complex Detection (MCODE) score. Interestingly, we found a high functional similarity from the associated genes/proteins in the network with known radiation response genes.

conclusionThis network-based approach on DEGs of human lymphocytes upon response to ionizing radiation provides clues for an opportunity to improve therapeutic efficacy.

Indexed as

GO enrichmentLymphocytesProtein-protein interactionRadiationTP53

Identifiers

PMID33794574
PMCPMC8024183
OpenAlexW3137019250

What OpenQuestion holds

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LicenceCC BY-NC
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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.