Evidence map›Paper›PMID 38611096›Full record

ArticleCancers2024

Cisplatin-Resistant Urothelial Bladder Cancer Cells Undergo Metabolic Reprogramming beyond the Warburg Effect.

Julieta Afonso, Catarina Barbosa-Matos, Ricardo Silvestre, Joana Pereira-Vieira, Samuel Martins Gonçalves, Camille Mendes-Alves, Pier Parpot, Joana Pinto, Ângela Carapito, Paula Guedes de Pinho and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 10 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

13 authors at 4 institutions in 2 countries.

Julieta AfonsoLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0002-9748-3752
Catarina Barbosa-MatosLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0003-1031-4241
Ricardo SilvestreLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0002-9270-2717
Joana Pereira-VieiraLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0002-5413-3445
Samuel Martins GonçalvesLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.
Camille Mendes-AlvesCQUM, Centre of Chemistry, Chemistry Department, Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.
Pier ParpotCQUM, Centre of Chemistry, Chemistry Department, Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.
Joana PintoAssociate Laboratory i4HB-Institute for Health and Bioeconomy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0001-9719-8364
Ângela CarapitoAssociate Laboratory i4HB-Institute for Health and Bioeconomy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0003-1396-4485
Paula Guedes de PinhoAssociate Laboratory i4HB-Institute for Health and Bioeconomy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-7395-5700
Lúcio SantosExperimental Pathology and Therapeutics Group, Research Center of the Portuguese Institute of Oncology (CI-IPOP), 4200-072 Porto, Portugal.
Adhemar Longatto-FilhoLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0002-5779-9752
Fátima BaltazarLife and Health Sciences Research Institute (ICVS), Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0002-1770-4544
University of Minho · PTUniversidade do Porto · PTHospital de Câncer de Barretos · BRInstituto Português de Oncologia Francisco Gentil · PT

Funding

Associate Laboratory i4HB project LA/P/0140/2020ERDF under the scope of NORTE 2020 UID/BIO/04469/2020, UID/QUI/0686/2020 and BioTecNorte operation (NORTE-01-0145-FEDER-000004)Foundation for Science and Technology (FCT) Fellowships SFRH/BPD/116784/2016 and SFRH/BD/145955/2019, and contract 2020.00185.CEECINDFoundation for Science and Technology (FCT) projects UIDB/50026/2020 and UIDP/50026/2020National funds from the FCT in the scope of the UCIBIO projects UIDP/04378/2020 and UIDB/04378/2020Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) NORTE-01-0145-FEDER-000055
6 · The paper itself

Abstract

Advanced urothelial bladder cancer (UBC) patients are tagged by a dismal prognosis and high mortality rates, mostly due to their poor response to standard-of-care platinum-based therapy. Mediators of chemoresistance are not fully elucidated. This work aimed to study the metabolic profile of advanced UBC, in the context of cisplatin resistance. Three isogenic pairs of parental cell lines (T24, HT1376 and KU1919) and the matching cisplatin-resistant (R) sublines were used. A set of functional assays was used to perform a metabolic screening on the cells. In comparison to the parental sublines, a tendency was observed towards an exacerbated glycolytic metabolism in the cisplatin-resistant T24 and HT1376 cells; this glycolytic phenotype was particularly evident for the HT1376/HT1376R pair, for which the cisplatin resistance ratio was higher. HT1376R cells showed decreased basal respiration and oxygen consumption associated with ATP production; in accordance, the extracellular acidification rate was also higher in the resistant subline. Glycolytic rate assay confirmed that these cells presented higher basal glycolysis, with an increase in proton efflux. While the results of real-time metabolomics seem to substantiate the manifestation of the Warburg phenotype in HT1376R cells, a shift towards distinct metabolic pathways involving lactate uptake, lipid biosynthesis and glutamate metabolism occurred with time. On the other hand, KU1919R cells seem to engage in a metabolic rewiring, recovering their preference for oxidative phosphorylation. In conclusion, cisplatin-resistant UBC cells seem to display deep metabolic alterations surpassing the Warburg effect, which likely depend on the molecular signature of each cell line.

Indexed as

cisplatin resistanceglucoseglutamatelactatelipid metabolismurothelial bladder cancerWarburg effect

Identifiers

PMID38611096
PMCPMC11010907
OpenAlexW4393993052

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.