Evidence map›Paper›PMID 27050073›Full record

ArticleOncotarget2016

Lysyl oxidase family activity promotes resistance of pancreatic ductal adenocarcinoma to chemotherapy by limiting the intratumoral anticancer drug distribution.

Benjamin Le Calvé, Audrey Griveau, David Vindrieux, Raphaël Maréchal, Clotilde Wiel, Magali Svrcek, Johann Gout, Lamia Azzi, Léa Payen, Jérôme Cros and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

51 citing papers in PubMed, 73 citations in OpenAlex.

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  15. What is new in cancer-associated fibroblast biomarkers?Cell communication and signaling : CCS · 2023
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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

16 authors at 7 institutions in 2 countries.

Benjamin Le CalvéInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Audrey GriveauInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
David VindrieuxInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Raphaël MaréchalDepartment of Gastroenterology and Gastrointestinal Cancer Unit, Erasme Hospital, Université Libre de Bruxelles, Belgium.
Clotilde WielInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Magali SvrcekDepartment of Pathology, AP-HP, Hôpitaux Universitaires Est Parisien, Saint-Antoine Hospital, Paris, France.
Johann GoutInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Lamia AzziService de Biologie des Tumeurs, CHU de Bordeaux Hôpital du Haut Lévêque, Pessac, France.
Léa PayenInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Jérôme CrosAP-HP, Hôpitaux Universitaires Paris Nord Val de Seine, Beaujon, France.
Christelle de la FouchardièreCentre Léon Bérard, Lyon, France.
Pierre DubusService de Biologie des Tumeurs, CHU de Bordeaux Hôpital du Haut Lévêque, Pessac, France.
Jérôme GuittonUniversité de Lyon, Lyon, France.
Laurent BartholinInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Jean-Baptiste BachetSorbonne University, UPMC University and INSERM, UMRS 1147, Paris Descrates University, Paris, France.
David BernardInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Université Claude Bernard Lyon 1 · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Léon Bérard · FRDélégation Paris 5 · FRDélégation Paris 7 · FRSorbonne Université · FRUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid tumors often display chemotherapy resistance. Pancreatic ductal adenocarcinoma (PDAC) is the archetype of resistant tumors as current chemotherapies are inefficient. The tumor stroma and extracellular matrix (ECM) are key contributors to PDAC aggressiveness and to limiting the efficacy of chemotherapy. Lysyl oxidase (LOX) family members mediate collagen cross-linking and thus promote ECM stiffening. Our data demonstrate increased LOX, LOXL1, and LOXL2 expression in PDAC, and that the level of fibrillar collagen, which is directly dependent of LOX family activity, is an independent predictive biomarker of adjuvant "Gemcitabine-based chemotherapy" benefit. Experimentally in mice, increased LOX family activity through LOXL2 promotes chemoresistance. This effect of LOX family activity seems to be due to decreased gemcitabine intra-tumoral diffusion. This observation might be explained by increased fibrillar collagen and decreased vessel size observed in tumors with increased LOX family activity. In conclusion, our data support that LOX family activity is both a novel target to improve chemotherapy as well as a novel biomarker to predict gemcitabine benefit in PDAC. Beyond the PDAC, it is possible that targeting LOX family activity might improve efficacy of chemotherapies against different kinds of solid tumors.

Indexed as

Drug Resistance, NeoplasmAmino Acid OxidoreductasesAnimalsAntimetabolites, AntineoplasticBiomarkers, TumorCarcinoma, Pancreatic DuctalCell Line, TumorDeoxycytidineDiffusionFemaleFibrillar CollagensGemcitabineGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansMice, NudeAmino Acid OxidoreductasesAntimetabolites, AntineoplasticBiomarkers, TumorDeoxycytidineFibrillar CollagensGemcitabineLOXL1 protein, humanLOXL2 protein, humanProtein-Lysine 6-Oxidasebiomarkerchemoresistancecollagenlysyl oxidasesurvival

Identifiers

PMID27050073
PMCPMC5078000
OpenAlexW2321472906

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.