Evidence map›Paper›PMID 24937674›Full record

ArticleBritish journal of cancer2014

Src, a potential target for overcoming trastuzumab resistance in HER2-positive breast carcinoma.

G Peiró, F Ortiz-Martínez, A Gallardo, A Pérez-Balaguer, J Sánchez-Payá, J J Ponce, A Tibau, L López-Vilaro, D Escuin, E Adrover and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of cancer, 2014. 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
5.1field-weighted citation impact, top 3% 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, 93 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

G Peiró1] Department of Pathology, University General Hospital of Alicante, Pintor Baeza 12, Alicante 03010, Spain [2] Research Unit, University General Hospital of Alicante, Pintor Baeza 12, Alicante 03010, Spain.
F Ortiz-MartínezResearch Unit, University General Hospital of Alicante, Pintor Baeza 12, Alicante 03010, Spain.
A GallardoDepartment of Pathology, Clinica Girona, Joan Maragall 16, Girona 17003, Spain.
A Pérez-BalaguerResearch Unit, University General Hospital of Alicante, Pintor Baeza 12, Alicante 03010, Spain.
J Sánchez-PayáDepartment of Epidemiology, University General Hospital of Alicante, Pintor Baeza 12, Alicante 03010, Spain.
J J PonceDepartment of Clinical Oncology, University General Hospital of Alicante, Pintor Baeza 12, Alicante 03010, Spain.
A TibauDepartment of Clinical Oncology, Hospital de la Santa Creu i Sant Pau, Sant Quintí 87-89, Barcelona 08041, Spain.
L López-VilaroDepartment of Pathology, Hospital de la Santa Creu i Sant Pau, Sant Quintí 87-89, Barcelona 08041, Spain.
D EscuinInstitut d'Investigacions Biomèdiques, Hospital de la Santa Creu i Sant Pau, Sant Quintí 87-89, Barcelona 08041, Spain Barcelona, Spain.
E AdroverDepartment of Clinical Oncology, University General Hospital of Albacete, Hermanos Falcó s/n, Albacete 02006, Spain.
A BarnadasDepartment of Clinical Oncology, Hospital de la Santa Creu i Sant Pau, Sant Quintí 87-89, Barcelona 08041, Spain.
E LermaDepartment of Pathology, Hospital de la Santa Creu i Sant Pau, Sant Quintí 87-89, Barcelona 08041, Spain.
Hospital de Sant Pau · ESHospital General Universitario de Alicante Doctor Balmis · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSrc is a non-receptor tyrosine kinase involved in signalling and crosstalk between growth-promoting pathways. We aim to investigate the relationship of active Src in response to trastuzumab of HER2-positive breast carcinomas.

methodsWe selected 278 HER2-positive breast cancer patients with (n=154) and without (n=124) trastuzumab treatment. We performed immunohistochemistry on paraffin-embedded tissue microarrays of active Src and several proteins involved in the PI3K/Akt/mTOR pathway, PIK3CA mutational analysis and in vitro studies (SKBR3 and BT474 cancer cells). The results were correlated with clinicopathological factors and patients' outcome.

resultsIncreased pSrc-Y416 was demonstrated in trastuzumab-resistant cells and in 37.8% of tumours that correlated positively with tumour size, necrosis, mitosis, metastasis to the central nervous system, p53 overexpression and MAPK activation but inversely with EGFR and p27. Univariate analyses showed an association of increased active Src with shorter survival in patients at early stage with HER2/hormone receptor-negative tumours treated with trastuzumab.

conclusionsSrc activation participates in trastuzumab mechanisms of resistance and indicates poor prognosis, mainly in HER2/hormone receptor-negative breast cancer. Therefore, blocking this axis may be beneficial in those patients.

Indexed as

AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBreast NeoplasmsCell Line, TumorCentral Nervous System NeoplasmsChemotherapy, AdjuvantClass I Phosphatidylinositol 3-KinasesDNA Mutational AnalysisDrug Resistance, NeoplasmEnzyme ActivationErb-b2 Receptor Tyrosine KinasesFemaleHumansAntibodies, Monoclonal, HumanizedAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPhosphatidylinositol 3-KinasesPIK3CA protein, humansrc-Family KinasesTrastuzumab

Identifiers

PMID24937674
PMCPMC4134494
OpenAlexW2100271152

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.