Evidence map›Paper›PMID 40650799›Full record

ReviewStem cell reviews and reports2025

Stem Cell for Cancer Immunotherapy: Current Approaches and Challenges.

Zainab Alali, Umme Tamanna Ferdous, Alexis Nzila, Farhana Easmin, Adnan Shakoor, Abdul Wasy Zia, Shihab Uddin

Abstract readReview
In one paragraph

Review in Stem cell reviews and reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Zainab AlaliDepartment of Bioengineering, King Fahd University of Petroleum & Minerals, 31261, Dhahran, Saudi Arabia.
Umme Tamanna FerdousCenter for Biosystems and Machines, King Fahd University of Petroleum & Minerals, 31261, Dhahran, Saudi Arabia.
Alexis NzilaDepartment of Bioengineering, King Fahd University of Petroleum & Minerals, 31261, Dhahran, Saudi Arabia.
Farhana EasminDepartment of Biological Engineering, Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA, 02139, USA.
Adnan ShakoorCenter for Biosystems and Machines, King Fahd University of Petroleum & Minerals, 31261, Dhahran, Saudi Arabia.
Abdul Wasy ZiaInstitute of Mechanical, Process, and Energy Engineering (IMPEE), School of Engineering and Physical Sciences, Heriot-Watt University, Edinburgh, EH14 4AS, UK. a.zia@hw.ac.uk.
Shihab UddinDepartment of Bioengineering, King Fahd University of Petroleum & Minerals, 31261, Dhahran, Saudi Arabia. shihab.uddin@kfupm.edu.sa.

Funding

King Fahd University of Petroleum and Minerals ISBN2504
6 · The paper itself

Abstract

Stem cell-based immunotherapy represents a groundbreaking advancement in cancer treatment, leveraging the immune system's inherent capacity to target and eradicate cancer cells. This review explores some of the examples of stem cells used in cancer immunotherapy, including hematopoietic, mesenchymal, and induced pluripotent stem cells (IPSCs). It also describes stem cell functionalities like modifying tumor microenvironment (TME) and developing engineered immune cells like chimeric antigen receptor (CAR)-T cells and natural killer (NK) cells. Additionally, the clinical applications of stem cells for improving cancer immunotherapies and delivering drugs directly to solid tumors are discussed. However, several challenges limit the effectiveness of stem cell technology, including safety risks, tumor avoidance by the immune system, and regulatory protocols as well as manufacturing barriers. This article reviews current advancements to overcome these challenges, such as CRISPR-based gene editing and targeted drug delivery systems and provides an outlook on emerging trends, such as the progress of personalized stem cell therapies and the increasing effectiveness of treatment by combining them with other cancer treatments.

Indexed as

ImmunotherapyNeoplasmsStem CellsAnimalsGene EditingHumansReceptors, Chimeric AntigenTumor MicroenvironmentReceptors, Chimeric AntigenCancerCAR-T cellsCRISPRImmunotherapyMicroenvironmentStem cells

Identifiers

PMID40650799
PMCPMC12408727

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.