Evidence map›Paper›PMID 22653144›Full record

ArticleBritish journal of cancer2012

NT5E CpG island methylation is a favourable breast cancer biomarker.

C Lo Nigro, M Monteverde, S Lee, L Lattanzio, D Vivenza, A Comino, N Syed, A McHugh, H Wang, C Proby and 10 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  15. The roles of CD73 in cancer.BioMed research international · 2014
    Review
  16. Article
  17. CD73 promotes anthracycline resistance and poor prognosis in triple negative breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  18. Review
  19. 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

20 authors at 7 institutions in 4 countries.

C Lo NigroLaboratory of Cancer Genetics and Translational Oncology, Oncology Department, S. Croce General Hospital, Cuneo, Italy.
M Monteverde
S Lee
L Lattanzio
D Vivenza
A Comino
N Syed
A McHugh
H Wang
C Proby
O Garrone
M Merlano
E Hatzimichael
E Briasoulis
O Gojis
C Palmieri
L Jordan
P Quinlan
A Thompson
T Crook
University of Dundee · GBAzienda Sanitaria Ospedaliera S.Croce e Carle Cuneo · ITNinewells Hospital · GBImperial College London · GBUniversity of Ioannina · GRCancer Research UK · GBThe Francis Crick Institute · GB

Funding

Cancer Research UK 13044
6 · The paper itself

Abstract

backgroundRelapse risk assessment and individual treatment recommendations remain suboptimal for breast cancer patients. In the light of existing preclinical and clinical data, we studied NT5E (5'-nucleotidase, ecto) expression and NT5E CpG island methylation in breast cancer.

methodsWe used RT-PCR, qPCR, methylation-specific PCR and pyrosequencing to analyse NT5E in breast carcinoma cell lines and primary and breast carcinomas.

resultsNT5E CpG island methylation was inversely associated with NT5E expression in breast carcinoma cell lines. In clinical series, patients whose primary tumours had NT5E CpG island methylation were less likely to develop metastasis (P=0.003, OR=0.34, 95% CI: 0.17-0.69). In 3/4 paired samples, NT5E was methylated in primary tumours and demethylated in CNS metastases. Patients progressing to non-visceral as compared with visceral metastases were more likely to have NT5E CpG island methylation in primary tumours (P=0.01, OR=11.8). Patients with tumours lacking detectable methylation had shorter disease-free survival (DFS) (P=0.001, HR=2.7) and overall survival (OS) (P=0.001, HR=3). The favourable prognostic value of NT5E methylation was confirmed in oestrogen receptor negative (P=0.011, HR=3.27, 95% CI: 1.31-8.12) and in triple negative cases (P=0.004; HR=6.2, 95% CI: 1.9-20). Moreover, we observed a more favourable outcome to adjuvant chemotherapy in patients whose tumours were positive for NT5E CpG island methylation: DFS (P=0.0016, HR=5.1, 95% CI: 1.8-14.37) and OS (P=0.0005, HR=7.4, 95% CI: 2.416-23.08).

conclusionNT5E CpG island methylation is a promising breast cancer biomarker.

Indexed as

DNA Methylation5'-NucleotidaseBiomarkers, TumorBreast NeoplasmsCell Line, TumorCpG IslandsDisease-Free SurvivalFemaleGene SilencingGPI-Linked ProteinsHumansNeoplasm MetastasisPrognosisPromoter Regions, Genetic5'-NucleotidaseBiomarkers, TumorGPI-Linked ProteinsNT5E protein, human

Identifiers

PMID22653144
PMCPMC3389412
OpenAlexW2053537854

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.