Evidence map›Paper›PMID 35669852›Full record

ArticleOxidative medicine and cellular longevity2022

Exosomal CXCL14 Contributes to M2 Macrophage Polarization through NF-

Hong-Yang Tian, Qi Liang, Zhen Shi, Hang Zhao

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 48 citations in OpenAlex.

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  19. Exploring G Protein-Coupled Receptors in Hematological Cancers.ACS pharmacology & translational science · 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

4 authors at 1 institution in 1 country.

Hong-Yang TianDepartment of Urology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Qi LiangDepartment of Urology Surgery, Dalinghe Hospital Affiliated to Medical College of Jinzhou Medical University, Jinzhou 121206, China.
Zhen ShiDepartment of Urology Surgery, Dalinghe Hospital Affiliated to Medical College of Jinzhou Medical University, Jinzhou 121206, China.
Hang ZhaoDepartment of Hepatobiliary Diseases, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.ORCID https://orcid.org/0000-0003-0523-0721
Jinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokine (C-X-C motif) ligand 14 (CXCL14) plays a critical role in maintaining homeostasis and inflammation in the local cell environment and regulating cancer progression. However, the role of CXCL14 in prostate cancer (PC) has not been fully investigated. In this study, the expression of CXCL14 was determined in PC tumor tissues by qRT-PCR and immunohistochemistry assay. Wound healing, invasion, colony formation, cell proliferation, and apoptosis assays were performed to evaluate the role of CXCL14 in PC progression. Exosomes were isolated from PC cell-condition medium by using ultracentrifugation assay and identified by using transmission electron microscopy and nanoparticle tracking analysis. M2 macrophage polarization-associated genes were measured by using qRT-PCR and Western blot assays. A PC xenograft mouse model was used to assess the role of CXCL14 in tumor growth in vivo. The results showed that CXCL14 was significantly upregulated in PC tissues and was positively correlated with pathological stages, lymph node metastasis, and angiolymphatic invasion. The positive correlations were also observed between CXCL14 and PD-L1 and IL-10. Knockdown CXCL14 dramatically inhibited PC cell proliferation, invasion, and colony formation, but not apoptosis. CXCL14 promoted M2 macrophage polarization through the NF-

Indexed as

MicroRNAsProstatic NeoplasmsAnimalsCell Line, TumorCell ProliferationChemokines, CXCHumansMacrophage ActivationMacrophagesMaleMiceNF-kappa BSignal TransductionChemokines, CXCCXCL14 protein, humanCXCL14 protein, mouseMicroRNAsNF-kappa B

Identifiers

PMID35669852
PMCPMC9166984
OpenAlexW4281688732

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.