Evidence map›Paper›PMID 40759634›Full record

ReviewSignal transduction and targeted therapy2025

Cancer stem cells: landscape, challenges and emerging therapeutic innovations.

Haksoo Lee, Byeongsoo Kim, Junhyeong Park, Sujin Park, Gaeun Yoo, Soomin Yum, Wooseok Kang, Jae-Myung Lee, HyeSook Youn, BuHyun Youn

Abstract readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 1 pooled it
–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

120 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Polysaccharides and carbohydrate polymers: innovations from nature to industry.Journal of the science of food and agriculture · 2026
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60 more citing papers are in PubMed but not listed here.

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

10 authors.

Haksoo Lee *Department of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Byeongsoo Kim *Department of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Junhyeong Park *Department of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Sujin ParkDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Gaeun YooDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Soomin YumDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Wooseok KangDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Jae-Myung LeeDepartment of Naval Architecture and Ocean Engineering, Pusan National University, Busan, Republic of Korea.
HyeSook YounDepartment of Integrative Bioscience and Biotechnology, Sejong University, Seoul, Republic of Korea.
BuHyun YounDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea. bhyoun72@pusan.ac.kr.ORCID 0000-0002-8010-519X

Funding

National Research Foundation of Korea (NRF) No. RS-2023-00301938National Research Foundation of Korea (NRF) RS-2023-00207904
6 · The paper itself

Abstract

Cancer stem cells (CSCs) constitute a highly plastic and therapy-resistant cell subpopulation within tumors that drives tumor initiation, progression, metastasis, and relapse. Their ability to evade conventional treatments, adapt to metabolic stress, and interact with the tumor microenvironment makes them critical targets for innovative therapeutic strategies. Recent advances in single-cell sequencing, spatial transcriptomics, and multiomics integration have significantly improved our understanding of CSC heterogeneity and metabolic adaptability. Metabolic plasticity allows CSCs to switch between glycolysis, oxidative phosphorylation, and alternative fuel sources such as glutamine and fatty acids, enabling them to survive under diverse environmental conditions. Moreover, interactions with stromal cells, immune components, and vascular endothelial cells facilitate metabolic symbiosis, further promoting CSC survival and drug resistance. Despite substantial progress, major hurdles remain, including the lack of universally reliable CSC biomarkers and the challenge of targeting CSCs without affecting normal stem cells. The development of 3D organoid models, CRISPR-based functional screens, and AI-driven multiomics analysis is paving the way for precision-targeted CSC therapies. Emerging strategies such as dual metabolic inhibition, synthetic biology-based interventions, and immune-based approaches hold promise for overcoming CSC-mediated therapy resistance. Moving forward, an integrative approach combining metabolic reprogramming, immunomodulation, and targeted inhibition of CSC vulnerabilities is essential for developing effective CSC-directed therapies. This review discusses the latest advancements in CSC biology, highlights key challenges, and explores future perspectives on translating these findings into clinical applications.

Indexed as

NeoplasmsNeoplastic Stem CellsTumor MicroenvironmentAnimalsDrug Resistance, NeoplasmHumans

Identifiers

PMID40759634
PMCPMC12322150

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.