Evidence map›Paper›PMID 40937397›Full record

ArticleIndian journal of clinical biochemistry : IJCB2025

Plasma-Derived Exosomal tRF-Phe-GAA-001 and tRF-Gly-GCC-037 as Novel Diagnostic Biomarkers for Cervical Cancer.

Zheng Li, Hongyan Wang, Ruijun Yang, Xiangchun Jin, Qing Han, Zhaoyuan She, Peng Ge

Abstract read
In one paragraph

Article in Indian journal of clinical biochemistry : IJCB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

  1. Transcriptomic and functional analysis of fibroid extracellular vesicles.Clinical science (London, England : 1979) · 2026
    Article
  2. 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

7 authors.

Zheng LiDepartment of Clinical Laboratory, Tianjin Medical University Cancer Institute and Hospital: Tianjin Tumor Hospital, Tianjin, China.
Hongyan WangDepartment of Clinical Laboratory, Tianjin Cancer Hospital Airport Hospital, National Clinical Research Center for Cancer, No. 99 East Fifth Road, Airport Economic Zone, Tianjin, China.
Ruijun YangDepartment of Clinical Laboratory, Tianjin Cancer Hospital Airport Hospital, National Clinical Research Center for Cancer, No. 99 East Fifth Road, Airport Economic Zone, Tianjin, China.
Xiangchun JinDepartment of Clinical Laboratory, Tianjin Cancer Hospital Airport Hospital, National Clinical Research Center for Cancer, No. 99 East Fifth Road, Airport Economic Zone, Tianjin, China.
Qing HanDepartment of Clinical Laboratory, Tianjin Cancer Hospital Airport Hospital, National Clinical Research Center for Cancer, No. 99 East Fifth Road, Airport Economic Zone, Tianjin, China.
Zhaoyuan SheDepartment of Clinical Laboratory, Tianjin Cancer Hospital Airport Hospital, National Clinical Research Center for Cancer, No. 99 East Fifth Road, Airport Economic Zone, Tianjin, China.
Peng GeDepartment of Clinical Laboratory, Tianjin Medical University Cancer Institute and Hospital: Tianjin Tumor Hospital, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study delves into the exploration of exosomal transfer RNA-derived fragments (tRFs) as potential diagnostic markers for cervical cancer (CC). Employing plasma-derived exosomes isolated through ultracentrifugation and confirmed via transmission electron microscopy (TEM), qNano, and western blot analysis, we extracted total RNA from CC and adjacent tissues (n = 48), alongside exosomes from cervical cancer patients (n = 140) and healthy donors (n = 140) using Trizol reagents. The expression of exosomal tRFs was assessed through quantitative polymerase chain reaction (qPCR) and subjected to statistical analysis using Mann-Whitney U or t-tests, along with receiver operating characteristic (ROC) analysis. The findings unveiled a significant downregulation of exosomal tRF-Phe-GAA-001 and tRF-Gly-GCC-037 in both CC tissues and plasma samples from early-stage patients compared to healthy controls. Remarkably, these two exosomal tRFs exhibited promising capabilities as circulating biomarkers for both the diagnosis and early detection of CC, as evidenced by their high area under the curve (AUC) values of 0.9337 and 0.9432, respectively. Consequently, exosomal tRF-Phe-GAA-001 and tRF-Gly-GCC-037 were downregulated in CC and early-stage CC, indicating their potential as innovative non-invasive biomarkers for early CC diagnosis. Supplementary Information: The online version contains supplementary material available at 10.1007/s12291-024-01235-7.

Indexed as

BiomarkerCervical cancerDerived fragments (tRFs)ExosomestRF-Gly-GCC-037tRF-Phe-GAA-001tRNA

Identifiers

PMID40937397
PMCPMC12420557

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.