Evidence map›Paper›PMID 34218325›Full record

ArticleJournal of cancer research and clinical oncology2021

Human umbilical cord mesenchymal stem cells-derived exosomal microRNA-181a retards nasopharyngeal carcinoma development by mediating KDM5C.

Jin Liu, Mingyi Zhu, Qianli Tang

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
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  4. Non-coding RNA and drug resistance in head and neck cancer.Cancer drug resistance (Alhambra, Calif.) · 2024
    Review
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  8. Targeting epigenetic regulators to overcome drug resistance in cancers.Signal transduction and targeted therapy · 2023
    Review
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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

3 authors at 2 institutions in 1 country.

Jin LiuSchool of the Integrated Traditional Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha, 410128, China.
Mingyi ZhuDepartment of Pathophysiology, Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China.
Qianli TangHunan University of Chinese Medicine, No.113 Shaoshan Middle Road, Changsha, 410208, Hunan, China. liujin_1983@163.com.ORCID http://orcid.org/0000-0003-1842-6985
Hunan University of Traditional Chinese Medicine · CNAffiliated Hospital of Youjiang Medical University for Nationalities · CN

Funding

2018 Guangxi scholarship Fund of Guangxi Education Department; Special Funding for Guangxi Special Experts No. GRCT[2019]13#Basic Ability Improvement Project for young and middle-aged Teachers in Universities of Guangxi NO. 2018KY0451Guangxi Medical High-level Leading Talents Training "139" Project No. GWKJ[2018] 22#The Self-funded Research Projects of National Health and Family Planning Commission of Guangxi NO. Z20170226
6 · The paper itself

Abstract

objectiveIt has been studied that mesenchymal stem cells (MSCs)-derived exosomes could suppress tumor growth in nasopharyngeal carcinoma (NPC) and microRNA-181a (miR-181a) could mediate drug resistance in NPC. Focused on this work, the mechanism of human umbilical cord MSCs (hUC-MSCs)-derived exosomal miR-181a was explored in NPC cell progression.

methodsNPC tissues and normal tissues were obtained from patients, and miR-181a and KDM5C expression was examined. hUC-MSCs-derived exosomes were extracted, identified and co-cultured with NPC cells (C666-1 and SUNE1). C666-1 cell progression in vitro and/or tumor growth in vivo were examined after incubation with exosomes, miR-181a or lysine-specific demethylase 5C (KDM5C). miR-181a and KDM5C expression were examined in NPC.

resultsmiR-181a expression was reduced while KDM5C expression was elevated in NPC. hUC-MSCs-derived exosomes restrained NPC cell growth in vivo and in vitro. Depleting or restoring exosomal miR-181a promoted or delayed NPC cell progression. KDM5C silencing suppressed NPC cell progression.

conclusionThis study concluded that hUC-MSCs-derived exosomal miR-181a retards NPC development via negatively modulating KDM5C, serving as a candidate reference for the therapy of NPC.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAged, 80 and overAnimalsApoptosisBiomarkers, TumorCell MovementCell ProliferationExosomesFemaleHistone DemethylasesHumansMaleMesenchymal Stem CellsMesenchymal Stem Cell TransplantationBiomarkers, TumorHistone DemethylasesKDM5C protein, humanMicroRNAsMIrn181 microRNA, humanExosomesHuman umbilical cord mesenchymal stem cellsLysine specific demethylase 5CMicroRNA-181aNasopharyngeal carcinoma

Identifiers

PMID34218325
PMCPMC11802003
OpenAlexW3182064359

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.