Evidence map›Paper›PMID 40855526›Full record

ArticleBMC infectious diseases2025

Plasma exosomal miR-122-5p_R-1, miR-23b-3p_R + 1, and miR-15a-5p_R-1 are associated with multidrug-resistant tuberculosis.

Yang Zhang, Linyu Zhang, Liying Shi, Liliang Wei, Lin Gan, Yuting Hu, Huai Huang, Keping Xie, Tingting Jiang, Ji-Cheng Li

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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. Article
  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

10 authors.

Yang Zhang *Center for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China.
Linyu Zhang *Center for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China.
Liying Shi *Department of Clinical Laboratory, Zhejiang Hospital, 310030, Hangzhou, China.
Liliang WeiDepartment of Pneumology, Affiliated Hospital of Shaoxing University, 312000, Shaoxing, China.
Lin GanCenter for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China.
Yuting HuCenter for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China.
Huai HuangCenter for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China.
Keping XieCenter for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China. mcxiekeping@scut.edu.cn.
Tingting JiangCenter for Pancreatic Cancer Research, The South China University of Technology School of Medicine, 382 Waihuan Road, Guangzhou, Guangdong, 510006, China. ttjiang@scut.edu.cn.
Ji-Cheng LiInstitute of Cell Biology, Zhejiang University, Hangzhou, 310031, China. Zjulijicheng@163.com.

Funding

Guangzhou Ruiqian Biological Technology Co., LTD 20230330The Zhejiang Province Traditional Chinese Medicine Science and Technology Plan Project 2025072985
6 · The paper itself

Abstract

backgroundPatients with multidrug-resistant tuberculosis (MDR-TB) who are resistant to at least both rifampicin and isoniazid, lack effective treatment options in clinic. The gold standard for the diagnosis of MDR-TB is drug sensitivity test, which is time-consuming and has a relatively low positive detection rate. Screening early diagnostic biomarker for MDR-TB is urgent need in clinical practice.

methodsA total of 33 patients with MDR-TB, healthy controls and drug-sensitive tuberculosis (DS-TB) were included in this study. Total plasma exosomal RNA was extracted from the subjects, and the MDR-TB plasma-specific exosomal miRNAs were obtained by Illumina sequencing.

resultsThere were 644 and 647 differentially expressed miRNAs in the plasma exosomes of MDR-TB patients obtained by sequencing and biogenic analysis compared with DS-TB patients and healthy controls, respectively. Differential miRNAs are mainly involved in the biological function of regulation of transcription and protein binding, and enriched in the pathways in cancer and MAPK signaling pathway. Moreover, seven plasma exosomal miRNAs in MDR-TB patients were significantly different from those in DS-TB patients and healthy controls. Among them, three of the miRNAs (hsa-miR-122-5p_R-1, hsa-miR-23b-3p_R + 1, and hsa-miR-15a-5p_R-1) were found to be in target relationship with MDR-TB related genes (NTRK2, KIDINS220, NCKAP1, MAPK9, NFAT5, ATF6 and SLC11A2) by target gene prediction analysis. Further the bioinformatic analysis showed that hsa-miR-122-5p_R-1 targets the protein PGLYRP2, a diagnostic biomarker identified in our previous study.

conclusionsWe suggest that hsa-miR-122-5p_R-1, hsa-miR-23b-3p_R + 1, and hsa-miR-15a-5p_R-1 are closely related to MDR-TB.

Indexed as

ExosomesMicroRNAsTuberculosis, Multidrug-ResistantAdultAgedBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedBiomarkersMicroRNAsMIRN122 microRNA, humanMIRN15 microRNA, humanBiomarker.ExosomeMDR-TBMiRNAPlasma

Identifiers

PMID40855526
PMCPMC12376478

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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.