Evidence map›Paper›PMID 33539530›Full record

ArticleBriefings in bioinformatics2021

Diseasome and comorbidities complexities of SARS-CoV-2 infection with common malignant diseases.

Md Shahriare Satu, Md Imran Khan, Md Rezanur Rahman, Koushik Chandra Howlader, Shatabdi Roy, Shuvo Saha Roy, Julian M W Quinn, Mohammad Ali Moni

Open access · bronzeAbstract read
In one paragraph

Article in Briefings in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 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

8 authors at 5 institutions in 2 countries.

Md Shahriare SatuDepartment of Management Information Systems, Noakhali Science & Technology University, Bangladesh.
Md Imran KhanDepartment of Computer Science and Engineering, Gono Bishwabidyalay, Bangladesh.
Md Rezanur RahmanDepartment of Biochemistry and Biotechnology, School of Biomedical Science, Khwaja Yunus Ali University, Enayetpur, Sirajganj, Bangladesh.
Koushik Chandra HowladerDepartment of Computer Science and Telecommunication Engineering, Noakhali Science & Technology University, Bangladesh.
Shatabdi RoyDepartment of Computer Science and Telecommunication Engineering, Noakhali Science & Technology University, Bangladesh.
Shuvo Saha RoyDepartment of Computer Science and Telecommunication Engineering, Noakhali Science & Technology University, Bangladesh.
Julian M W QuinnThe Garvan Institute of Medical Research, Healthy Ageing Theme, Darlinghurst, NSW, Australia.
Mohammad Ali MoniDepartment of Management Information Systems, Noakhali Science & Technology University, Bangladesh.
Noakhali Science and Technology University · BDGarvan Institute of Medical Research · AUGono University · BDIslamic University · BDUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the increasing number of immunoinflammatory complexities, cancer patients have a higher risk of serious disease outcomes and mortality with SARS-CoV-2 infection which is still not clear. In this study, we aimed to identify infectome, diseasome and comorbidities between COVID-19 and cancer via comprehensive bioinformatics analysis to identify the synergistic severity of the cancer patient for SARS-CoV-2 infection. We utilized transcriptomic datasets of SARS-CoV-2 and different cancers from Gene Expression Omnibus and Array Express Database to develop a bioinformatics pipeline and software tools to analyze a large set of transcriptomic data and identify the pathobiological relationships between the disease conditions. Our bioinformatics approach revealed commonly dysregulated genes (MARCO, VCAN, ACTB, LGALS1, HMOX1, TIMP1, OAS2, GAPDH, MSH3, FN1, NPC2, JUND, CHI3L1, GPNMB, SYTL2, CASP1, S100A8, MYO10, IGFBP3, APCDD1, COL6A3, FABP5, PRDX3, CLEC1B, DDIT4, CXCL10 and CXCL8), common gene ontology (GO), molecular pathways between SARS-CoV-2 infections and cancers. This work also shows the synergistic complexities of SARS-CoV-2 infections for cancer patients through the gene set enrichment and semantic similarity. These results highlighted the immune systems, cell activation and cytokine production GO pathways that were observed in SARS-CoV-2 infections as well as breast, lungs, colon, kidney and thyroid cancers. This work also revealed ribosome biogenesis, wnt signaling pathway, ribosome, chemokine and cytokine pathways that are commonly deregulated in cancers and COVID-19. Thus, our bioinformatics approach and tools revealed interconnections in terms of significant genes, GO, pathways between SARS-CoV-2 infections and malignant tumors.

Indexed as

COVID-19Gene OntologyHumansNeoplasmsSARS-CoV-2Signal TransductionTranscriptomecancerscomorbiditiesCOVID-19

Identifiers

PMID33539530
PMCPMC7929360
OpenAlexW3126184947

What OpenQuestion holds

Textmetadata
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.