Evidence map›Paper›PMID 41756775›Full record

ReviewChemical & biomedical imaging2026

Lighting Up Endogenous RNA: Fluorescent Aptamer Sensors for Live-Cell Imaging.

Zhe Ma, Kulsoom, Fu Wang

Abstract readReview
In one paragraph

Review in Chemical & biomedical imaging, 2026. 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. Resolving Sub-Nuclear Architecture from Compartments to Functional Domains.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
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.

Zhe MaDepartment of Urology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
KulsoomDepartment of Urology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Fu WangDepartment of Urology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID https://orcid.org/0000-0001-9222-0833

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endogenous RNAs orchestrate cellular processes through precise spatiotemporal regulation, and live-cell imaging of these molecules is essential for dissecting their roles in gene expression, disease progression, and cellular homeostasis. While traditional methods rely on exogenous labeling or fixation, fluorescent RNA aptamer-based sensors have emerged as transformative tools for visualizing endogenous RNAs in their native context. These sensors allow real-time tracking of mRNA localization, miRNA activity, and RNA-protein interactions with minimal disturbance. However, challenges such as the requirement for exogenous fluorogenic dyes, limited brightness, photostability, and target specificity in complex cellular environments hinder their wider application. This review provides a comprehensive overview of recent advances in fluorescent RNA aptamer-based sensors, discussing the design principles, mechanisms of fluorescence activation, and their application in live-cell RNA imaging. We also address the current limitations and future directions for improving these sensors, highlighting their transformative potential in RNA biology and their implications for diagnostic and therapeutic strategies.

Indexed as

BiosensorsFluorogenic DyesImagingRNA AptamersRNA Dynamics

Identifiers

PMID41756775
PMCPMC12933491

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.