Evidence map›Paper›PMID 34339312›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2021

SPM Receptor Expression and Localization in Irradiated Salivary Glands.

Harim Tavares Dos Santos, Kihoon Nam, Jason P Hunt, Luke O Buchmann, Marcus M Monroe, Olga J Baker

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 54% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Review
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 2 institutions in 1 country.

Harim Tavares Dos SantosDepartment of Otolaryngology-Head and Neck Surgery, University of Missouri, Columbia, Missouri.
Kihoon NamDepartment of Otolaryngology-Head and Neck Surgery, University of Missouri, Columbia, Missouri.
Jason P HuntDepartment of Otolaryngology, Department of Surgery, The University of Utah, Salt Lake City, Utah.
Luke O BuchmannDepartment of Otolaryngology, Department of Surgery, The University of Utah, Salt Lake City, Utah.
Marcus M MonroeDepartment of Otolaryngology, Department of Surgery, The University of Utah, Salt Lake City, Utah.
Olga J BakerDepartment of Otolaryngology-Head and Neck Surgery, University of Missouri, Columbia, Missouri.
University of Missouri · USUniversity of Utah · US

Funding

A Targeted Approach to Managing Salivary Gland Inflammation Using ResolvinsR01DE027884 · NIDCR · UNIVERSITY OF UTAH · PI BAKER, OLGA JULIANA · 2018 to 2022
$1.7M
NIDCR NIH HHS R01 DE027884
6 · The paper itself

Abstract

Radiation therapy-mediated salivary gland destruction is characterized by increased inflammatory cell infiltration and fibrosis, both of which ultimately lead to salivary gland hypofunction. However, current treatments (e.g., artificial saliva and sialagogues) only promote temporary relief of symptoms. As such, developing alternative measures against radiation damage is critical for restoring salivary gland structure and function. One promising option for managing radiation therapy-mediated damage in salivary glands is by activation of specialized proresolving lipid mediator receptors due to their demonstrated role in resolution of inflammation and fibrosis in many tissues. Nonetheless, little is known about the presence and function of these receptors in healthy and/or irradiated salivary glands. Therefore, the goal of this study was to detect whether these specialized proresolving lipid mediator receptors are expressed in healthy salivary glands and, if so, if they are maintained after radiation therapy-mediated damage. Our results indicate that specialized proresolving lipid mediator receptors are heterogeneously expressed in inflammatory as well as in acinar and ductal cells within human submandibular glands and that their expression persists after radiation therapy. These findings suggest that epithelial cells as well as resident immune cells represent potential targets for modulation of resolution of inflammation and fibrosis in irradiated salivary glands.

Indexed as

Radiation ToleranceAcinar CellsAdultAgedEndothelial CellsFemaleGamma RaysGene ExpressionHumansLeukocytes, MononuclearMaleMiddle AgedReceptors, ChemokineReceptors, Formyl PeptideReceptors, G-Protein-CoupledReceptors, Leukotriene B4CMKLR1 protein, humanFPR2 protein, humanGPR32 protein, humanLTB4R protein, humanReceptors, ChemokineReceptors, Formyl PeptideReceptors, G-Protein-CoupledReceptors, Leukotriene B4Receptors, Lipoxinfibrosisinflammationradiation therapyspecialized proresolving lipid mediators

Identifiers

PMID34339312
PMCPMC8335844
OpenAlexW3191849856

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.