Evidence map›Paper›PMID 33572276›Full record

ArticleCancers2021

Inhibition of Mitochondrial Dynamics Preferentially Targets Pancreatic Cancer Cells with Enhanced Tumorigenic and Invasive Potential.

Sarah Courtois, Beatriz de Luxán-Delgado, Laure Penin-Peyta, Alba Royo-García, Beatriz Parejo-Alonso, Petra Jagust, Sonia Alcalá, Juan A Rubiolo, Laura Sánchez, Bruno Sainz and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 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

12 authors at 5 institutions in 3 countries.

Sarah CourtoisTranslational Research Unit, Hospital Universitario Miguel Servet, IIS Aragon, 50009 Zaragoza, Spain.
Beatriz de Luxán-DelgadoCentre for Stem Cells in Cancer & Ageing, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK.
Laure Penin-PeytaCentre for Stem Cells in Cancer & Ageing, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK.
Alba Royo-GarcíaTranslational Research Unit, Hospital Universitario Miguel Servet, IIS Aragon, 50009 Zaragoza, Spain.
Beatriz Parejo-AlonsoTranslational Research Unit, Hospital Universitario Miguel Servet, IIS Aragon, 50009 Zaragoza, Spain.ORCID 0000-0002-5393-4283
Petra JagustCentre for Stem Cells in Cancer & Ageing, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK.
Sonia AlcaláDepartment of Biochemistry, School of Medicine, Instituto de Investigaciones Biomédicas (IIBm) "Alberto Sols" CSIC-UAM, Autónoma University of Madrid (UAM), 28029 Madrid, Spain.
Juan A RubioloDepartment of Zoology, Genetics and Physical Anthropology, Veterinary Faculty, Universidad de Santiago de Compostela, 27002 Lugo, Spain.
Laura SánchezDepartment of Zoology, Genetics and Physical Anthropology, Veterinary Faculty, Universidad de Santiago de Compostela, 27002 Lugo, Spain.ORCID 0000-0001-7927-5303
Bruno SainzDepartment of Biochemistry, School of Medicine, Instituto de Investigaciones Biomédicas (IIBm) "Alberto Sols" CSIC-UAM, Autónoma University of Madrid (UAM), 28029 Madrid, Spain.ORCID 0000-0003-4829-7651
Christopher HeeschenCenter for Single-Cell Omics & State Key Laboratory of Oncogenes and Related Genes, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Patricia SanchoTranslational Research Unit, Hospital Universitario Miguel Servet, IIS Aragon, 50009 Zaragoza, Spain.ORCID 0000-0002-1092-5395
Hospital Universitario Miguel Servet · ESQueen Mary University of London · GBInstituto de Investigaciones Biomédicas Sols-Morreale · ESUniversidade de Santiago de Compostela · ESShanghai Jiao Tong University · CN

Funding

Fundación Científica Asociación Española Contra el Cáncer 19-0250Fundación Científica Asociación Española Contra el Cáncer GC16173694BARBInstituto de Salud Carlos III CP16/00121Instituto de Salud Carlos III PI17/00082Pancreatic Cancer Research Fund 2015 Award RoundSeventh Framework Programme 602783Worldwide Cancer Research 19-0250
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the deadliest tumors, partly due to its intrinsic aggressiveness, metastatic potential, and chemoresistance of the contained cancer stem cells (CSCs). Pancreatic CSCs strongly rely on mitochondrial metabolism to maintain their stemness, therefore representing a putative target for their elimination. Since mitochondrial homeostasis depends on the tightly controlled balance between fusion and fission processes, namely mitochondrial dynamics, we aim to study this mechanism in the context of stemness. In human PDAC tissues, the mitochondrial fission gene

Indexed as

cancer stem cellsCD133DRP1energy crisismitochondriamitochondrial dynamicsmitochondrial fissionpancreatic cancerPDAC

Identifiers

PMID33572276
PMCPMC7914708
OpenAlexW3128417170

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.