Evidence map›Paper›PMID 42536274›Full record

ReviewInternational journal of clinical oncology2026

Current therapeutic interventions to target cancer stem cells for metastasis.

Priyancka Arora, Rakesh Bhatia, Sheetal Sharma, Anupam Sharma, Subhash C Chauhan, Jagmohan Singh, Anil Kumar Sharma

Abstract readReview
PubMed Publisher
In one paragraph

Review in International journal of clinical 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

7 authors.

Priyancka AroraDepartment of Biotechnology, Amity School of Biological Sciences, Amity University Punjab, Sector 82A, IT City, International Airport Road, Sahibzada Ajit Singh Nagar, Punjab, 140306, India.
Rakesh BhatiaDepartment of Biotechnology, Amity School of Biological Sciences, Amity University Punjab, Sector 82A, IT City, International Airport Road, Sahibzada Ajit Singh Nagar, Punjab, 140306, India. rbhatia@pb.amity.edu.
Sheetal SharmaDepartment of Experimental Medicine and Biotechnology, PGIMER Chandigarh, Chandigarh, 160012, India.
Anupam SharmaDepartment of Physics, Guru Kashi University, Talwandi Sabo, Bathinda, Punjab, India.
Subhash C ChauhanDepartment of Microbiology and Immunology, School of Medicine, University of Texas Rio Grande Valley (UTRGV), Edinburg, TX, 78504, USA.
Jagmohan SinghDepartment of Biotechnology, Amity School of Biological Sciences, Amity University Punjab, Sector 82A, IT City, International Airport Road, Sahibzada Ajit Singh Nagar, Punjab, 140306, India.
Anil Kumar SharmaDepartment of Biotechnology, Amity School of Biological Sciences, Amity University Punjab, Sector 82A, IT City, International Airport Road, Sahibzada Ajit Singh Nagar, Punjab, 140306, India. anibiotech18@gmail.com.ORCID http://orcid.org/0000-0002-9768-1644

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer metastasis contributes to the high mortality rate in patients and remains a significant challenge in treating solid malignancies. The limitations of current therapeutic interventions are underscored by the mere 5% survivorship of patients with metastatic disease. Since cancer stem cells (CSCs) are the major cause of metastatic spread, emerging therapeutic modalities specifically targeting CSCs present a lucrative approach to curtail metastatic disease. The literature demonstrating the promise of targeting CSCs to limit metastatic spread holds immense potential but remains scattered. This review provides concise knowledge of CSC targeting strategies and their impact on the metastatic burden in cancer patients. Current therapeutic strategies, early screening of cancer and reduction in smoking have drastically reduced the cancer-associated deaths by 34% in the US [1]. However, CSCs and therapy resistance pose major clinical challenges. Therefore, new way to address CSCs such as targeting stemness pathways, cellular plasticity and stress tolerance, nano theranostic approaches, the effect of phytochemicals and new radiotherapy technologies such as microbeam radiotherapy are being extensively studied. The detailed molecular studies on CSCs provide a platform for identifying factors intrinsic to cancer cells, host cells, and tumor microenvironment (TME) influencing stemness and overall metastasis. In addition to emerging anti-metastasis therapeutic modalities, the review provides information regarding exclusive targets and signalling molecules involved in metastasis. Simultaneous targeting of factors regulating CSCs and TME, along with standard of care therapies, proves a better strategy to tackle CSC heterogeneity and their adaptation for metastatic disease. Further approaches impacting CSCs offer a promising avenue for enhancing the effectiveness of cancer therapeutics and discovering new anti-metastatic drug candidates.

Indexed as

Neoplasm MetastasisNeoplasmsNeoplastic Stem CellsAnimalsAntineoplastic AgentsHumansMolecular Targeted TherapyTumor MicroenvironmentAntineoplastic AgentsCancer stem cellsMetastasisMicrobeam radiotherapyNanotheranosticsPhytochemicalsSignaling pathwaysSurface markersTumor-associated antigensTumor phenotypic plasticity

Identifiers

What OpenQuestion holds

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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.