Evidence map›Paper›PMID 35057091›Full record

ArticlePharmaceutics2022

Induction of Immunogenic Cell Death by Photodynamic Therapy Mediated by Aluminum-Phthalocyanine in Nanoemulsion.

Mosar Corrêa Rodrigues, Wellington Tavares de Sousa Júnior, Thayná Mundim, Camilla Lepesqueur Costa Vale, Jaqueline Vaz de Oliveira, Rayane Ganassin, Thyago José Arruda Pacheco, José Athayde Vasconcelos Morais, João Paulo Figueiró Longo, Ricardo Bentes Azevedo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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

21 citing papers in PubMed, 37 citations in OpenAlex.

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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 at 1 institution in 1 country.

Mosar Corrêa RodriguesLaboratory of Nanoscience and Immunology, Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.
Wellington Tavares de Sousa JúniorDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia 70910-900, Brazil.
Thayná MundimDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia 70910-900, Brazil.
Camilla Lepesqueur Costa ValeDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia 70910-900, Brazil.
Jaqueline Vaz de OliveiraLaboratory of Nanoscience and Immunology, Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.ORCID 0000-0002-9173-0433
Rayane GanassinLaboratory of Nanoscience and Immunology, Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.
Thyago José Arruda PachecoLaboratory of Nanoscience and Immunology, Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.ORCID 0000-0002-8090-0644
José Athayde Vasconcelos MoraisLaboratory of Nanoscience and Immunology, Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.ORCID 0000-0003-3067-4842
João Paulo Figueiró LongoDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia 70910-900, Brazil.ORCID 0000-0002-5154-7263
Ricardo Bentes AzevedoDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia 70910-900, Brazil.ORCID 0000-0002-2137-9588
Luis Alexandre MuehlmannLaboratory of Nanoscience and Immunology, Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.
Universidade de Brasília · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior 01Foundation for Research Support of the Federal District 0193.001020/2015Foundation for Research Support of the Federal District 0193.001626/2017Foundation for Research Support of the Federal District PRONEXNational Council for Scientific and Technological Development 0447628/2014-3National Council for Scientific and Technological Development 193.001.200/2016
6 · The paper itself

Abstract

Photodynamic therapy (PDT) has been clinically employed to treat mainly superficial cancer, such as basal cell carcinoma. This approach can eliminate tumors by direct cytotoxicity, tumor ischemia, or by triggering an immune response against tumor cells. Among the immune-related mechanisms of PDT, the induction of immunogenic cell death (ICD) in target cells is to be cited. ICD is an apoptosis modality distinguished by the emission of damage-associated molecular patterns (DAMP). Therefore, this study aimed to analyze the immunogenicity of CT26 and 4T1 treated with PDT mediated by aluminum-phthalocyanine in nanoemulsion (PDT-AlPc-NE). Different PDT-AlPc-NE protocols with varying doses of energy and AlPc concentrations were tested. The death mechanism and the emission of DAMPs-CRT, HSP70, HSP90, HMGB1, and IL-1β-were analyzed in cells treated in vitro with PDT. Then, the immunogenicity of these cells was assessed in an in vivo vaccination-challenge model with BALB/c mice. CT26 and 4T1 cells treated in vitro with PDT mediated by AlPc IC

Indexed as

apoptosisdamage associated molecules patternsimmunotherapynanobiotechnology

Identifiers

PMID35057091
PMCPMC8778058
OpenAlexW4205913767

What OpenQuestion 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 OpenQuestion graph.