Evidence map›Paper›PMID 33318476›Full record

ArticleCell death & disease2020

Distinct photo-oxidation-induced cell death pathways lead to selective killing of human breast cancer cells.

Ancély F Dos Santos, Alex Inague, Gabriel S Arini, Letícia F Terra, Rosangela A M Wailemann, André C Pimentel, Marcos Y Yoshinaga, Ricardo R Silva, Divinomar Severino, Daria Raquel Q de Almeida and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 61 citations in OpenAlex.

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  16. Over-Expressed GATA-1Antioxidants (Basel, Switzerland) · 2023
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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

16 authors at 2 institutions in 1 country.

Ancély F Dos SantosDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Alex InagueDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.ORCID 0000-0001-7410-9226
Gabriel S AriniDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Letícia F TerraDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Rosangela A M WailemannDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
André C PimentelDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.ORCID 0000-0001-7254-3803
Marcos Y YoshinagaDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Ricardo R SilvaFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo (USP), Ribeirão Preto, 14040-903, Brazil.
Divinomar SeverinoDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.ORCID 0000-0001-9483-6287
Daria Raquel Q de AlmeidaDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Vinícius M GomesDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Alexandre Bruni-CardosoDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Walter R TerraDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Sayuri MiyamotoDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil.
Maurício S BaptistaDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil. baptista@iq.usp.br.ORCID 0000-0001-7079-7666
Leticia LabriolaDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo (USP), São Paulo, 05508-000, Brazil. labriola@iq.usp.br.ORCID 0000-0003-3899-6088
Universidade de São Paulo · BRUniversidade de Ribeirão Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lack of effective treatments for aggressive breast cancer is still a major global health problem. We have previously reported that photodynamic therapy using methylene blue as photosensitizer (MB-PDT) massively kills metastatic human breast cancer, marginally affecting healthy cells. In this study, we aimed to unveil the molecular mechanisms behind MB-PDT effectiveness and specificity towards tumor cells. Through lipidomics and biochemical approaches, we demonstrated that MB-PDT efficiency and specificity rely on polyunsaturated fatty acid-enriched membranes and on the better capacity to deal with photo-oxidative damage displayed by non-tumorigenic cells. We found out that, in tumorigenic cells, lysosome membrane permeabilization is accompanied by ferroptosis and/or necroptosis. Our results also pointed at a cross-talk between lysosome-dependent cell death (LDCD) and necroptosis induction after photo-oxidation, and contributed to broaden the understanding of MB-PDT-induced mechanisms and specificity in breast cancer cells. Therefore, we demonstrated that efficient approaches could be designed on the basis of lipid composition and metabolic features for hard-to-treat cancers. The results further reinforce MB-PDT as a therapeutic strategy for highly aggressive human breast cancer cells.

Indexed as

LightAntioxidantsBreast NeoplasmsCarcinogenesisCell DeathCell Line, TumorFemaleFerroptosisHumansLipidsLysosomesMethylene BlueModels, BiologicalNecroptosisOxidation-ReductionPhotochemotherapyAntioxidantsLipidsMethylene Blue

Identifiers

PMID33318476
PMCPMC7736888
OpenAlexW3111553647

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.