Evidence map›Paper›PMID 36683230›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Boosting the Potential of Chemotherapy in Advanced Breast Cancer Lung Metastasis via Micro-Combinatorial Hydrogel Particles.

Anna Lisa Palange, Daniele Di Mascolo, Miguel Ferreira, Peter J Gawne, Raffaele Spanò, Alessia Felici, Luca Bono, Thomas Lee Moore, Marco Salerno, Andrea Armirotti and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
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

11 authors.

Anna Lisa PalangeLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Daniele Di MascoloLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Miguel FerreiraLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Peter J GawneLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Raffaele SpanòLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Alessia FeliciLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Luca BonoAnalytical Chemistry Facility, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Thomas Lee MooreLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Marco SalernoMaterials Characterization Facility, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Andrea ArmirottiAnalytical Chemistry Facility, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.
Paolo DecuzziLaboratory of Nanotechnology for Precision Medicine, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, Genoa, 16163, Italy.ORCID 0000-0001-6050-4188

Funding

European Research CouncilEuropean Union's Horizon 2020 754490European Union's Seventh Framework Programme 616695European Union's Seventh Framework Programme FP7/2007-2013Italian Association for Cancer Research 17664
6 · The paper itself

Abstract

Breast cancer cell colonization of the lungs is associated with a dismal prognosis as the distributed nature of the disease and poor permeability of the metastatic foci challenge the therapeutic efficacy of small molecules, antibodies, and nanomedicines. Taking advantage of the unique physiology of the pulmonary circulation, here, micro-combinatorial hydrogel particles (µCGP) are realized via soft lithographic techniques to enhance the specific delivery of a cocktail of cytotoxic nanoparticles to metastatic foci. By cross-linking short poly(ethylene glycol) (PEG) chains with erodible linkers within a shape-defining template, a deformable and biodegradable polymeric skeleton is realized and loaded with a variety of therapeutic and imaging agents, including docetaxel-nanoparticles. In a model of advanced breast cancer lung metastasis, µCGP amplified the colocalization of docetaxel-nanoparticles with pulmonary metastatic foci, prolonged the retention of chemotoxic molecules at the diseased site, suppressed lesion growth, and boosted survival beyond 20 weeks post nodule engraftment. The flexible design and modular architecture of µCGP would allow the efficient deployment of complex combination therapies in other vascular districts too, possibly addressing metastatic diseases of different origins.

Indexed as

Antineoplastic AgentsBreast NeoplasmsLung NeoplasmsDocetaxelFemaleHumansHydrogelsAntineoplastic AgentsDocetaxelHydrogelsdocetaxeldrug deliveryhydrogelspulmonary metastasissoft lithographytheranostics

Identifiers

PMID36683230
PMCPMC10074128

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.