Evidence map›Paper›PMID 42426902›Full record

ReviewJournal of hematology & oncology2026

Cancer stem cell plasticity: mechanisms, immune microenvironment crosstalk, and therapeutic implications.

Jingyu Tan, Tao Wen, Jian Liu, Xiaoli Ru

Abstract readReview
In one paragraph

Review in Journal of hematology & oncology, 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

4 authors.

Jingyu TanMedical Research Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China.
Tao WenMedical Research Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China.
Jian LiuMedical Research Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China. liujian2004811@126.com.
Xiaoli RuDepartment of Gynecology and Obstetrics, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China. 18801350216@163.com.

Funding

National Natural Science Foundation of China No. 82473039
6 · The paper itself

Abstract

Cancer stem cells (CSCs) represent functionally defined and phenotypically plastic tumor cell populations implicated in therapeutic resistance, relapse, and metastasis. CSC plasticity is regulated through coordinated stemness signaling and epigenetic mechanisms. Canonical stemness-associated pathways, including Wnt, Notch, and Hedgehog, interact with epigenetic programs to maintain dynamic stem-like states and facilitate cellular adaptation to environmental and therapeutic stress. These regulatory networks are also associated with metabolic reprogramming and may support CSC survival under therapeutic and immune pressure. This review summarizes recent advances in our understanding of CSC plasticity, with a particular focus on the bidirectional interplay between CSCs and the tumor immune microenvironment. From a translational perspective, it further summarizes emerging strategies for targeting CSC plasticity in combination with immunotherapy, and discusses the present limitations and challenges of combination strategies. These observations may provide a conceptual framework for the development of more rational combination strategies, although their clinical benefit remains to be validated.

Indexed as

Cell PlasticityNeoplasmsNeoplastic Stem CellsTumor MicroenvironmentAnimalsHumansImmunotherapySignal TransductionCancer plasticityCancer stem cellImmune evasionImmunotherapyTumor immune microenvironment

Identifiers

PMID42426902
PMCPMC13536802

What Socratic holds

Textmetadata
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.