Evidence map›Paper›PMID 41152935›Full record

ReviewMolecular cancer2025

Advances in engineering immune-tumor microenvironments on-a-chip: integrative microfluidic platforms for immunotherapy and drug discovery.

Farnaz Dabbagh Moghaddam, Ali Anvar, Ehsan Ilkhani, Delara Dadgar, Maedeh Rafiee, Najmeh Ranjbaran, Pejman Mortazavi, Seyed Majid Ghoreishian, Yun Suk Huh, Pooyan Makvandi

Abstract readReview
In one paragraph

Review in Molecular cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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  8. 3D Bioprinting Strategies in Autoimmune Disease Models.International journal of molecular sciences · 2025
    Review
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  10. 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

10 authors.

Farnaz Dabbagh Moghaddam *Institute for Photonics and Nanotechnologies, National Research Council, Via Fosso del Cavaliere, 100, Rome, 00133, Italy. Farnaz.dabbaghmoghaddam@cnr.it.
Ali Anvar *Blood Diseases Research Center (BDRC), Iranian Comprehensive Hemophilia Care Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Ehsan IlkhaniFaculty of Veterinary Medicine, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Delara DadgarDepartment of Veterinary Pathobiology, SR.C, Islamic Azad University, Tehran, Iran.
Maedeh RafieeDepartment of Veterinary Sciences, University of Wyoming, Snowy Range Road Laramie, Laramie, WY, 82070, USA.
Najmeh RanjbaranDepartment of Veterinary Pathobiology, SR.C, Islamic Azad University, Tehran, Iran.
Pejman MortazaviDepartment of Veterinary Pathobiology, SR.C, Islamic Azad University, Tehran, Iran.
Seyed Majid GhoreishianCenter for Energy and Environmental Solutions (CEES), College of STEM-T, South Carolina State University, Orangeburg, SC, 29117, USA.
Yun Suk HuhDepartment of Biological Sciences and Bioengineering, NanoBio High-Tech Materials Research Center, Inha University, Incheon, 22212, Republic of Korea. yunsuk.huh@inha.ac.kr.
Pooyan MakvandiThe Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, 324000, China. pooyanmakvandi@wmu.edu.cn.

Funding

National Research Foundation of Korea 2022R1C1C1005384
6 · The paper itself

Abstract

The design and application of microfluidic immune system-on-a-chip (ISOC) technology have played a critical role in cancer immunology and drug discovery over the past decades. The system provides a highly controlled and physiologically relevant platform for studying immune responses and therapeutic interventions. Emerging trends in 3D bioprinting, organoid fusion, and multi-organ systems-on-a-chip further expand the capabilities of ISOC by enabling systemic immune interactions and modeling of the tumor microenvironment. Despite these advances, scalability, standardization, and long-term immune cell viability remain significant challenges that must be addressed to fully harness the potential of ISOC in clinical applications. Overall, ISOC represents a transformative tool in cancer research, offering innovative solutions for immunotherapy trials, biomarker discovery, and precision medicine. Therefore, in this study, the role of ISOC in cancer immunotherapy was investigated, focusing on its ability to recapitulate primary and secondary immune functions, model immune-tumor interactions, and enhance screening and optimization of immune-based therapies. Device design and modeling strategies were also discussed, demonstrating how ISOC platforms simulate dynamic immune cell activity, cytokine signaling, and antigen presentation to improve drug efficacy assessments. The application of ISOC technology in drug discovery and its potential to accelerate clinical trials and develop personalized immunotherapy were further explored.

Indexed as

Drug DiscoveryImmunotherapyLab-On-A-Chip DevicesMicrofluidicsNeoplasmsTumor MicroenvironmentAnimalsHumansCancerDrug discoveryImmune-system-on-a-chipMicrofluidic device

Identifiers

PMID41152935
PMCPMC12560574

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.