Evidence map›Paper›PMID 25065595›Full record

ArticleOncogene2015

Immune-dependent antineoplastic effects of cisplatin plus pyridoxine in non-small-cell lung cancer.

F Aranda, N Bloy, J Pesquet, B Petit, K Chaba, A Sauvat, O Kepp, N Khadra, D Enot, C Pfirschke and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.4field-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

43 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
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  11. Metabolic features of cancer cells impact immunosurveillance.Journal for immunotherapy of cancer · 2021
    Article
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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.

F Aranda1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France.
N Bloy1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France [4] Université Paris Sud, Villejuif, France.
J Pesquet1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France.
B PetitINSERM U1030, Villejuif, France.
K Chaba1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
A Sauvat1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France.
O Kepp1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France.
N Khadra1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France.
D Enot1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France.
C PfirschkeCenter for Systems Biology, Massachusetts General Hospital/Harvard Medical School, Pittet Lab, Boston, MA, USA.
M PittetCenter for Systems Biology, Massachusetts General Hospital/Harvard Medical School, Pittet Lab, Boston, MA, USA.
L Zitvogel1] Université Paris Sud, Villejuif, France [2] INSERM U1015, Villejuif, France [3] Centre d'Investigation Clinique Biothérapie CICBT 507, Villejuif, France.
G Kroemer1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Paris, France [3] Metabolomics and Cell Biology Platforms, Villejuif, France [4] Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
L Senovilla1] Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, INSERM U1138, Paris, France [2] Metabolomics and Cell Biology Platforms, Villejuif, France [3] INSERM U1015, Villejuif, France.
Inserm · FRCentre de Recherche des Cordeliers · FRUniversité Paris Cité · FRCenter for Systems Biology · USMassachusetts General Hospital · USUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

cis-Diamminedichloroplatinum(II) (CDDP), which is mostly referred to as cisplatin, is a widely used antineoplastic. The efficacy of cisplatin can be improved by combining it with the vitamin B6 precursor pyridoxine. Here, we evaluated the putative synergistic interaction of CDDP with pyridoxine in the treatment of an orthotopic mouse model of non-small-cell lung cancer (NSCLC). CDDP and pyridoxine exhibited hyperadditive therapeutic effects. However, this synergy was only observed in the context of an intact immune system and disappeared when the otherwise successful drug combination was applied to the same NSCLC cancer implanted in the lungs of athymic mice (which lack T lymphocytes). Immunocompetent mice that had been cured from NSCLC by the combined regimen of CDDP plus pyridoxine became resistant against subcutaneous rechallenge with the same (but not with an unrelated) cancer cell line. In vitro, CDDP and pyridoxine did not only cause synergistic killing of NSCLC cells but also elicited signs of immunogenic cell death including an endoplasmic reticulum stress response and exposure of calreticulin at the surface of the NSCLC cells. NSCLC cells treated with CDDP plus pyridoxine in vitro elicited a protective anticancer immune response upon their injection into immunocompetent mice. Altogether, these results suggest that the combined regimen of cisplatin plus pyridoxine mediates immune-dependent antineoplastic effects against NSCLC.

Indexed as

AnimalsCalreticulinCarcinoma, Non-Small-Cell LungCell Line, TumorCisplatinDrug SynergismDrug Therapy, CombinationEndoplasmic Reticulum StressLung NeoplasmsMiceMice, SCIDNeoplasm TransplantationPyridoxineXenograft Model Antitumor AssaysCalreticulinCisplatinPyridoxine

Identifiers

PMID25065595
OpenAlexW2003801865

What OpenQuestion holds

Textmetadata
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.