Evidence map›Paper›PMID 41673894›Full record

ReviewCell communication and signaling : CCS2026

RNA G-quadruplexes in oncogene regulation and as emerging targets for cancer therapy.

Zi-Yan Liu, Xiao-Yan Wang, Dan-Dan Gong, Xuan Tang, Chang-Feng Man, Shi-Qi Zhang, Yu Fan

Abstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zi-Yan Liu *Cancer Institue, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, People's Republic of China.
Xiao-Yan Wang *Digestive Department, The Suqian Clinical College of Xuzhou Medical University, Suqian, Jiangsu, People's Republic of China.
Dan-Dan Gong *Cancer Institue, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, People's Republic of China.
Xuan TangCancer Institue, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, People's Republic of China.
Chang-Feng ManCancer Institue, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, People's Republic of China.
Shi-Qi ZhangDigestive Department, The Suqian Clinical College of Xuzhou Medical University, Suqian, Jiangsu, People's Republic of China.
Yu FanCancer Institue, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, People's Republic of China. yuf12345@ujs.edu.cn.

Funding

Key project fund of Jiangsu Provincial Health Commission ZD2022052, K2023016Suqian science and technology support project fund KY202203Zhenjiang Key Research and Development Fund SH2024002, SH2024075, JC2024031
6 · The paper itself

Abstract

RNA G-quadruplexes (rG4s) are RNA secondary structures formed by the folding of guanine-rich sequences. As emerging post-transcriptional regulatory elements, rG4s play crucial roles at multiple levels of gene expression regulation. In recent years, the pivotal roles of rG4s in cancer initiation and progression have gained increasing attention. In tumor biology, the structural stability and dynamic folding properties of rG4s directly influence the expression of key oncogenes, thereby regulating malignant phenotypes such as tumor cell proliferation, invasion, metastasis, and drug resistance. We summarize the diverse mechanisms by which rG4s regulate cancer-related genes and review recent advances in their roles in translational control, alternative splicing, mRNA stability, and noncoding RNA functions. Furthermore, we discuss emerging rG4-targeting technologies and their potential to specifically modulate rG4-mediated gene expression in tumors. Our aim is to provide new insights into the mechanisms of rG4 function in cancer and to offer novel strategies for developing targeted cancer therapies directed at specific rG4-containing transcripts.

Indexed as

Gene Expression Regulation, NeoplasticG-QuadruplexesMolecular Targeted TherapyNeoplasmsOncogenesRNAAnimalsHumansRNACancer gene regulationPost-transcriptional regulationrG4srG4-targeting ligandsTargeted therapy

Identifiers

PMID41673894
PMCPMC13001201

What OpenQuestion holds

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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.