Evidence map›Paper›PMID 33488608›Full record

ArticleFrontiers in immunology2020

Transcriptomic and Network Analysis of Minor Salivary Glands of Patients With Primary Sjögren's Syndrome.

Akinsola Oyelakin, Erich Horeth, Eun-Ah Christine Song, Sangwon Min, Monika Che, Brandon Marzullo, Christopher J Lessard, Astrid Rasmussen, Lida Radfar, R Hal Scofield and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 39 citations in OpenAlex.

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  16. Tlr7 drives sex- and tissue-dependent effects in Sjögren's disease.Frontiers in cell and developmental biology · 2024
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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

20 authors at 5 institutions in 1 country.

Akinsola OyelakinDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
Erich HorethDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
Eun-Ah Christine SongDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
Sangwon MinDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
Monika CheDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
Brandon MarzulloGenomics and Bioinformatics Core, State University of New York at Buffalo, Buffalo, NY, United States.
Christopher J LessardArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Astrid RasmussenArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Lida RadfarCollege of Dentistry, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.
R Hal ScofieldArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
David M LewisCollege of Dentistry, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.
Donald U StoneDean McGee Eye Institute, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.
Kiely GrundahlArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Scott S De RossiDental College of Georgia, Augusta University, Augusta, GA, United States.
Zoya KuragoDental College of Georgia, Augusta University, Augusta, GA, United States.
A Darise FarrisArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Kathy L SivilsArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Satrajit SinhaDepartment of Biochemistry, State University of New York at Buffalo, Buffalo, NY, United States.
Jill M KramerDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
Rose-Anne RomanoDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.
University at Buffalo, State University of New York · USOklahoma Medical Research Foundation · USUniversity of Oklahoma Health Sciences Center · USAugusta University · USDean McGee Eye Institute · US

Funding

Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TIMOTHY M VANWAGONER · 2013 to 2026
$68.2M
Advanced Training in Oral BiologyT32DE023526 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Stefan Hans-Klaus Ruhl · 2013 to 2026
$3.7M
Functional Evaluation of Established Sjogren's Syndrome Immune Response LociR01AR065953 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI LESSARD, CHRISTOPHER J · 2015 to 2018
$2.1M
NIAMS NIH HHS R01 AR065953NIDCR NIH HHS T32 DE023526NIGMS NIH HHS U54 GM104938
6 · The paper itself

Abstract

Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease characterized primarily by immune-mediated destruction of exocrine tissues, such as those of the salivary and lacrimal glands, resulting in the loss of saliva and tear production, respectively. This disease predominantly affects middle-aged women, often in an insidious manner with the accumulation of subtle changes in glandular function occurring over many years. Patients commonly suffer from pSS symptoms for years before receiving a diagnosis. Currently, there is no effective cure for pSS and treatment options and targeted therapy approaches are limited due to a lack of our overall understanding of the disease etiology and its underlying pathology. To better elucidate the underlying molecular nature of this disease, we have performed RNA-sequencing to generate a comprehensive global gene expression profile of minor salivary glands from an ethnically diverse cohort of patients with pSS. Gene expression analysis has identified a number of pathways and networks that are relevant in pSS pathogenesis. Moreover, our detailed integrative analysis has revealed a primary Sjögren's syndrome molecular signature that may represent important players acting as potential drivers of this disease. Finally, we have established that the global transcriptomic changes in pSS are likely to be attributed not only to various immune cell types within the salivary gland but also epithelial cells which are likely playing a contributing role. Overall, our comprehensive studies provide a database-enriched framework and resource for the identification and examination of key pathways, mediators, and new biomarkers important in the pathogenesis of this disease with the long-term goals of facilitating earlier diagnosis of pSS and to mitigate or abrogate the progression of this debilitating disease.

Indexed as

Gene Expression ProfilingGene Regulatory NetworksTranscriptomeCase-Control StudiesComputational BiologyEpithelial CellsFemaleHumansMiddle AgedSalivary Glands, MinorSjogren's Syndromebioinformaticsgene expressionRNA-sequencingsalivary glandSjögren’s syndrome

Identifiers

PMID33488608
PMCPMC7821166
OpenAlexW3118552580

What OpenQuestion holds

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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.