Evidence map›Paper›PMID 42866611›Full record

ReviewBiochemistry and biophysics reports2026

Engineered exosomes for breast cancer immunotherapy: Emerging strategies and translational potential.

Niloufar Orooji, Mahsa Ghasemian-Irani, Nasrin Salari, Tamana Eskandari, Mehrshad Shams, Fatemeh Tavassoli Razavi, Dariush Haghmorad

Abstract readReview
In one paragraph

Review in Biochemistry and biophysics reports, 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.

Niloufar OroojiCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Mahsa Ghasemian-IraniDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Nasrin SalariCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Tamana EskandariCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Mehrshad ShamsDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Fatemeh Tavassoli RazaviCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Dariush HaghmoradCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer remains one of the leading causes of cancer-related mortality in women worldwide, despite significant advances in early detection and conventional therapies. Immunotherapy has emerged as a promising strategy to harness the body's immune system to combat tumors. However, limitations such as immune escape mechanisms and inefficient drug delivery continue to challenge its effectiveness. In recent years, engineered exosomes, cell-derived nanoscale vesicles, have gained attention as innovative carriers for cancer immunotherapy due to their natural biocompatibility, low immunogenicity, and inherent targeting capabilities. This review highlights recent advancements in the design and functionalization of exosomes for breast cancer immunotherapy, including the loading of immune-stimulating molecules, genetic cargos, and surface modifications to enhance tumor specificity. We also discuss their advantages over conventional nanocarriers, immunological mechanisms, preclinical evidence, and challenges related to clinical translation. While significant progress has been made, further research is needed to overcome current barriers and fully exploit the potential of engineered exosomes as a next-generation platform in breast cancer immunotherapy.

Indexed as

Breast cancerEngineered exosomesExtracellular vesiclesImmunotherapyNanocarriersTargeted drug delivery

Identifiers

PMID42866611
PMCPMC13657104

What OpenQuestion holds

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Registered trials

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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.