Evidence map›Paper›PMID 38727266›Full record

ArticleCells2024

Tumor Microenvironment Modulates Invadopodia Activity of Non-Selected and Acid-Selected Pancreatic Cancer Cells and Its Sensitivity to Gemcitabine and C18-Gemcitabine.

Tiago M A Carvalho, Madelaine Magalì Audero, Maria Raffaella Greco, Marilena Ardone, Teresa Maggi, Rosanna Mallamaci, Barbara Rolando, Silvia Arpicco, Federico Alessandro Ruffinatti, Alessandra Fiorio Pla and 4 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  7. Review
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

14 authors.

Tiago M A CarvalhoDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.ORCID 0000-0001-9095-1413
Madelaine Magalì AuderoU1003 PHYCEL Laboratoire de Physiologie Cellulaire, Inserm, University of Lille, 59000 Lille, France.ORCID 0000-0003-0923-1481
Maria Raffaella GrecoDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.
Marilena ArdoneDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.ORCID 0009-0005-4233-9920
Teresa MaggiDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.
Rosanna MallamaciDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.ORCID 0000-0001-5966-5064
Barbara RolandoDepartment of Drug Science and Technology, University of Turin, 10125 Turin, Italy.ORCID 0000-0001-6138-1503
Silvia ArpiccoDepartment of Drug Science and Technology, University of Turin, 10125 Turin, Italy.ORCID 0000-0002-4754-6591
Federico Alessandro RuffinattiLaboratory of Cellular and Molecular Angiogenesis, Department of Life Sciences and Systems Biology, University of Turin, 10123 Turin, Italy.ORCID 0000-0002-3084-0380
Alessandra Fiorio PlaU1003 PHYCEL Laboratoire de Physiologie Cellulaire, Inserm, University of Lille, 59000 Lille, France.ORCID 0000-0003-4576-1594
Natalia PrevarskayaU1003 PHYCEL Laboratoire de Physiologie Cellulaire, Inserm, University of Lille, 59000 Lille, France.
Tomas KoltaiHospital del Centro Gallego de Buenos Aires, Buenos Aires 2199, Argentina.
Stephan J ReshkinDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.ORCID 0000-0001-9757-5908
Rosa Angela CardoneDepartment of Biosciences, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.ORCID 0000-0002-2011-9135

Funding

Marie Curie Innovative Training Program (ITN) "pH and Ion Transport in Pancreatic Cancer-pHioniC 813834; H2020-MSCA-ITN-2018National Center for Gene Therapy and Drugs based on RNA Technology - PNRR per la Missione 4, componente 2-investimento 1.4 CN00000041PRIN 2022 "AdaPtiviTy" 20227YTZE3PRIN 2022 PNRR "PhOXyOmicGEM" P2022L5HAZ
6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) is a deadly disease with high mortality due to early metastatic dissemination and high chemoresistance. All these factors are favored by its extracellular matrix (ECM)-rich microenvironment, which is also highly hypoxic and acidic. Gemcitabine (GEM) is still the first-line therapy in PDAC. However, it is quickly deaminated to its inactive metabolite. Several GEM prodrugs have emerged to improve its cytotoxicity. Here, we analyzed how the acidic/hypoxic tumor microenvironment (TME) affects the response of PDAC cell death and invadopodia-mediated ECM proteolysis to both GEM and its C18 prodrug.

methodsFor this, two PDAC cell lines, PANC-1 and Mia PaCa-2 were adapted to pH

resultsWe found that C18 has higher cytotoxic and anti-invadopodia activity than GEM in all culture conditions and especially in acid and hypoxic environments.

conclusionsWe propose C18 as a more effective approach to conventional GEM in developing new therapeutic strategies overcoming PDAC chemoresistance.

Indexed as

DeoxycytidineGemcitabinePancreatic NeoplasmsTumor MicroenvironmentCarcinoma, Pancreatic DuctalCell Line, TumorDrug Resistance, NeoplasmHumansPodosomesProdrugsDeoxycytidineGemcitabineProdrugscell invasionchemoresistanceextracellular acidosishypoxiainvadopodia

Identifiers

PMID38727266
PMCPMC11083398

What OpenQuestion holds

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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.