Evidence map›Paper›PMID 26036632›Full record

ArticleOncotarget2015

Exploiting the potential of autophagy in cisplatin therapy: A new strategy to overcome resistance.

Jesús García-Cano, Gorbatchev Ambroise, Raquel Pascual-Serra, Maria Carmen Carrión, Leticia Serrano-Oviedo, Marta Ortega-Muelas, Francisco J Cimas, Sebastià Sabater, María José Ruiz-Hidalgo, Isabel Sanchez Perez and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Insight into autophagy in platinum resistance of cancer.International journal of clinical oncology · 2023
    Review
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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

14 authors at 6 institutions in 2 countries.

Jesús García-CanoUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
Gorbatchev AmbroiseINSERM U.1197/Université Paris-Sud/Equipe Labellisée Ligue Nationale Contre le Cancer, Hôpital Paul Brousse, Villejuif, France.
Raquel Pascual-SerraUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
Maria Carmen CarriónDepartamento de Química Inorgánica, Orgánica y Bioquímica, UCLM. Facultad de Ciencias y Tecnologías Químicas-IRICA, Ciudad Real, Spain.
Leticia Serrano-OviedoUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
Marta Ortega-MuelasUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
Francisco J CimasUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
Sebastià SabaterRadiation Oncology Department, Complejo Hospitalario Universitario Albacete (CHUA), Spain.
María José Ruiz-HidalgoDepartamento de Química Orgánica, Inorgánica y Bioquímica, Facultad de Medicina, Albacete, Spain.
Isabel Sanchez PerezDepartment of Biochemistry, School of Medicine, UAM/Biomedical Research Institute of Madrid, Madrid CSIC/UAM, Madrid, Spain.
Antonio MasUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
Félix A JalónDepartamento de Química Inorgánica, Orgánica y Bioquímica, UCLM. Facultad de Ciencias y Tecnologías Químicas-IRICA, Ciudad Real, Spain.
Aimé VazquezINSERM U.1197/Université Paris-Sud/Equipe Labellisée Ligue Nationale Contre le Cancer, Hôpital Paul Brousse, Villejuif, France.
Ricardo Sánchez-PrietoUnidad de Medicina Molecular, Centro Regional de Investigaciones Biomédicas. Universidad de Castilla-La Mancha, Albacete, Spain.
University of Castilla-La Mancha · ESHospital General Universitario de Albacete · ESComplejo Hospitalario Universitario de Albacete · ESLa Ligue Contre le Cancer · FRUniversidad Autónoma de Madrid · ESUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistance to cisplatin is a major challenge in the current cancer therapy. In order to explore new therapeutic strategies to cisplatin resistance, we evaluated, in a model of lung cancer (H1299 and H460 cell lines), the nature of the pathways leading to cell death. We observed that H1299 displayed a natural resistance to cisplatin due to an inability to trigger an apoptotic response that correlates with the induction of autophagy. However, pharmacological and genetic approaches showed how autophagy was a mechanism associated to cell death rather than to resistance. Indeed, pro-autophagic stimuli such as mTOR or Akt inhibition mediate cell death in both cell lines to a similar extent. We next evaluated the response to a novel platinum compound, monoplatin, able to promote cell death in an exclusive autophagy-dependent manner. In this case, no differences were observed between both cell lines. Furthermore, in response to monoplatin, two molecular hallmarks of cisplatin response (p53 and MAPKs) were not implicated, indicating the ability of this pro-autophagic compound to overcome cisplatin resistance. In summary, our data highlight how induction of autophagy could be used in cisplatin resistant tumours and an alternative treatment for p53 mutated patient in a synthetic lethally approach.

Indexed as

Antineoplastic AgentsApoptosisAutophagyAutophagy-Related Protein 5Cell Line, TumorCisplatinDrug Resistance, NeoplasmHEK293 CellsHumansLung NeoplasmsMicrotubule-Associated ProteinsPlatinum CompoundsProto-Oncogene Proteins c-aktRNA InterferenceRNA, Small InterferingTOR Serine-Threonine KinasesAntineoplastic AgentsATG5 protein, humanAutophagy-Related Protein 5CisplatinMicrotubule-Associated ProteinsmonoplatinMTOR protein, humanPlatinum CompoundsProto-Oncogene Proteins c-aktRNA, Small InterferingTOR Serine-Threonine KinasesTP53 protein, humanTumor Suppressor Protein p53apoptosisautophagycisplatinmonoplatinsynthetic lethality

Identifiers

PMID26036632
PMCPMC4558170
OpenAlexW1561352174

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.