Evidence map›Paper›PMID 41935089›Full record

ReviewCell death & disease2026

Regulating the dormancy of cancer stem cells: a novel approach to preventing cancer relapse.

Qian Wang, Ning Liang, Xiongchao Fang, Tao Yang, Xianli He, Gang Wang, Nan Wang

Abstract readReview
In one paragraph

Review in Cell death & disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Qian Wang *Department of General Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.ORCID http://orcid.org/0000-0002-1904-7787
Ning Liang *Department of Gastroenterology, 920th Hospital of the Joint Logistics Support Force, PLA, Kunming, China.ORCID http://orcid.org/0000-0003-4201-9220
Xiongchao Fang *Department of General Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Tao Yang *Department of Interventional Radiology, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Xianli HeDepartment of General Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China. wanghe@fmmu.edu.cn.ORCID http://orcid.org/0000-0001-6869-9418
Gang WangDepartment of General Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China. wanggangfmmu@163.com.ORCID http://orcid.org/0009-0000-5047-1407
Nan WangDepartment of General Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China. wangnanafmu@163.com.ORCID http://orcid.org/0000-0003-1389-9900

Funding

Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2025A1515012583
6 · The paper itself

Abstract

Dormant cancer stem cells (CSCs) are the root cause of the drug resistance and metastatic processes of malignant tumors, but an in-depth analysis of their biological mechanisms is needed. Dormant CSCs are in the G0 phase of the cell cycle and are characterized by enhanced autophagic activity, a stable genomic structure and strong plasticity. Recently, several new specific markers of dormant CSCs, such as p27, CD13, QSOX1, Survivin, GPD1 and BEX2, have been identified, which offer hope for targeted therapy. In addition, epigenetic modifications such as DNA methylation and histone modifications have been reported to regulate the transition between the quiescent and proliferative states of dormant CSCs. From a clinical perspective, keeping cancer stem cells in a dormant state is helpful for preventing tumor recurrence and metastasis. To this end, clarifying the potential mechanisms and molecular regulation of cancer stem cell dormancy is vital. Here, in this review, we examine recent significant findings regarding tumor stem cell dormancy in both experimental and human disease models, emphasizing the underlying molecular mechanisms, regulatory processes, experimental models, and prospective research directions aimed at advancing this field and enhancing clinical translation.

Indexed as

Neoplasm Recurrence, LocalNeoplasmsNeoplastic Stem CellsAnimalsEpigenesis, GeneticHumans

Identifiers

PMID41935089
PMCPMC13186972

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.