Evidence map›Paper›PMID 42719025›Full record

ReviewFrontiers in bioengineering and biotechnology2026

Stimuli-responsive bioengineered platforms for precision cancer therapy.

Hossein Omidian, Renae L Wilson

Abstract readReview
In one paragraph

Review in Frontiers in bioengineering and biotechnology, 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

2 authors.

Hossein OmidianBarry and Judy Silverman College of Pharmacy, Nova Southeastern University, Fort Lauderdale, FL, United States.
Renae L WilsonBarry and Judy Silverman College of Pharmacy, Nova Southeastern University, Fort Lauderdale, FL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stimuli-responsive bioengineered platforms are redefining cancer therapy by shifting therapeutic design from systemic drug exposure toward context-dependent activation within malignant tissue. These systems are engineered to sense and respond to tumor-associated or externally applied cues, including acidic pH, redox imbalance, hypoxia, enzymatic activity, reactive oxygen species, temperature variation, light, ultrasound, and magnetic fields. Across the reviewed evidence, their principal value lies not merely in drug encapsulation but in the coordinated control of localization, release, intracellular access, multimodal therapy, microenvironment modulation, and safety. The field encompasses diverse architectures, including biomacromolecular nanoparticles, hydrogels, nanogels, polymeric micelles, prodrug assemblies, lipid-based systems, mesoporous silica, metal-organic frameworks, carbon-based materials, magnetic nanocomposites, and hybrid inorganic-organic constructs. These platforms have been validated in multiple cancer models through assays of uptake, cytotoxicity, apoptosis, spheroid penetration, tumor suppression, metastasis, recurrence, immune activation, stromal remodeling, and systemic tolerability. Collectively, the evidence supports a conceptual transition from passive nanocarriers to programmable therapeutic systems capable of aligning therapeutic action with the spatial, temporal, and biological heterogeneity of tumors. However, translation remains constrained by formulation complexity, incomplete standardization, limited long-term safety and biodistribution data, insufficient penetration into protected tumor niches, and the need for clinically relevant models that capture patient-level heterogeneity. Future progress will depend on rationally simplified architectures, quantitative stimulus-response validation, scalable manufacturing, integrated safety assessment, and biomarker-guided selection of platforms matched to defined tumor microenvironments. Stimuli-responsive bioengineering therefore represents a promising, although still maturing, foundation for safer, more selective, and more mechanistically coordinated precision cancer therapy.

Indexed as

bioengineered nanomedicinecontrolled drug deliverymultifunctional biomaterialsprecision oncologystimuli-responsive biomaterialsstimuli-responsive nanomedicinetranslational cancer bioengineeringtumor microenvironment

Identifiers

PMID42719025
PMCPMC13555214

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.