Evidence map›Paper›PMID 27835884›Full record

ArticleOncotarget2016

Combination of COX-2 expression and PIK3CA mutation as prognostic and predictive markers for celecoxib treatment in breast cancer.

Sandrine Tury, Véronique Becette, Franck Assayag, Sophie Vacher, Camille Benoist, Maud Kamal, Elisabetta Marangoni, Ivan Bièche, Florence Lerebours, Céline Callens

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 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.4field-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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. TMED2 as a marker of prognosis in breast cancer [Letter].Cancer management and research · 2019
    Article
  6. Article
  7. Article
  8. Expression of VEGF, COX-2 and MMP-9 in breast cancer and their relationship with ultrasound findings.International journal of clinical and experimental pathology · 2018
    Review
  9. New Immunotherapy Strategies in Breast Cancer.International journal of environmental research and public health · 2017
    Review
  10. Article
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

10 authors at 1 institution in 1 country.

Sandrine TuryPharmacogenomic Unit, Genetics Laboratory, Institut Curie, Paris, France.
Véronique BecetteDepartment of Pathology, Institut Curie, Hôpital René Huguenin, Saint-Cloud, France.
Franck AssayagLaboratory of Preclinical Investigations, Translational Research Department, Institut Curie, Paris, France.
Sophie VacherPharmacogenomic Unit, Genetics Laboratory, Institut Curie, Paris, France.
Camille BenoistPharmacogenomic Unit, Genetics Laboratory, Institut Curie, Paris, France.
Maud KamalDepartment of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
Elisabetta MarangoniLaboratory of Preclinical Investigations, Translational Research Department, Institut Curie, Paris, France.
Ivan BièchePharmacogenomic Unit, Genetics Laboratory, Institut Curie, Paris, France.
Florence LereboursDepartment of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
Céline CallensPharmacogenomic Unit, Genetics Laboratory, Institut Curie, Paris, France.
Institut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COX-2 expression level and prognostic value are still a matter of debate in breast cancer (BC). We addressed these points in the context of PIK3CA mutational status. Based on an interesting study of aspirin efficacy in colorectal cancer, we hypothesized that celecoxib antitumoral activity may be restricted to PIK3CA mutated BC.COX-2 mRNA expression was analyzed in 446 BC samples and in 61 BC patient-derived xenografts (PDX) using quantitative RT-PCR. The prognostic impact of COX-2 expression level was assessed independently and according to PIK3CA mutational status in our cohort and in a validation set of 817 BC. The antitumoral activity of celecoxib was tested in two triple-negative (TN) PDX with a PIK3CA wild-type (wt) or mutated genotype.COX-2 mRNA was overexpressed in 2% of BC and significantly associated with TN subtype. Metastasis-free survival (MFS) was significantly better in patients with high COX-2 expression level, the prognosis of whom was similar to patients with PIK3CA mutations. TCGA validation cohort confirmed that patients with low COX-2 expression PIK3CA wt tumors had the worse disease-free survival (DFS) compared to all other subgroups. Celecoxib had a significant antitumoral effect in PIK3CA mutated PDX only. Celecoxib antitumoral activity involved S6 ribosomal protein and AKT phosphorylation.Low expression of COX-2 has a significant negative impact on the MFS/DFS of BC patients. Antitumoral effect of celecoxib is restricted to PIK3CA mutated PDX. These results suggest that PIK3CA mutation may be a new predictive biomarker for celecoxib efficacy.

Indexed as

AdultAgedAged, 80 and overAnimalsAntineoplastic AgentsBiomarkers, PharmacologicalBreast NeoplasmsCelecoxibClass I Phosphatidylinositol 3-KinasesCyclooxygenase 2Cyclooxygenase 2 InhibitorsDNA Mutational AnalysisFemaleGene Expression Regulation, NeoplasticHumansMiceAntineoplastic AgentsBiomarkers, PharmacologicalCelecoxibClass I Phosphatidylinositol 3-KinasesCyclooxygenase 2Cyclooxygenase 2 InhibitorsPIK3CA protein, humanPTGS2 protein, humanbreast cancercelecoxibPIK3CApredictive biomarkerprognosis

Identifiers

PMID27835884
PMCPMC5356723
OpenAlexW2549207365

What OpenQuestion holds

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Registered trials

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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.