Evidence map›Paper›PMID 27449755›Full record

ArticleClinical & experimental metastasis2016

Frequent co-expression of EGFR and NeuGcGM3 ganglioside in cancer: it's potential therapeutic implications.

Addys González Palomo, Rancés Blanco Santana, Xiomara Escobar Pérez, Damián Blanco Santana, Mariano Rolando Gabri, Kalet León Monzon, Adriana Carr Pérez

Open access · hybridAbstract read
In one paragraph

Article in Clinical & experimental metastasis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 18 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

7 authors at 2 institutions in 2 countries.

Addys González PalomoCenter of Molecular Immunology (CIM), 216 Street and 15 Avenue, Atabey, Playa, P.O. Box 16040, Habana, Cuba. addys@cim.sld.cu.
Rancés Blanco SantanaCenter of Molecular Immunology (CIM), 216 Street and 15 Avenue, Atabey, Playa, P.O. Box 16040, Habana, Cuba.
Xiomara Escobar PérezDepartment of Cell Biology and Tissues Banking, National Institute of Oncology and Radiology, 29 and F Street, Vedado, Plaza de la Revolución, P.O. Box 10400, Havana, Cuba.
Damián Blanco SantanaDepartment of Cell Biology and Tissues Banking, National Institute of Oncology and Radiology, 29 and F Street, Vedado, Plaza de la Revolución, P.O. Box 10400, Havana, Cuba.
Mariano Rolando GabriLaboratory of Molecular Oncology, Quilmes National University, R. Sáenz Peña 180, P.O. Box B1876BXD, Buenos Aires, Argentina.
Kalet León MonzonCenter of Molecular Immunology (CIM), 216 Street and 15 Avenue, Atabey, Playa, P.O. Box 16040, Habana, Cuba.
Adriana Carr PérezCenter of Molecular Immunology (CIM), 216 Street and 15 Avenue, Atabey, Playa, P.O. Box 16040, Habana, Cuba.
Center of Molecular Immunology (Cuba) · CUNational University of Quilmes · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interaction between epidermal growth factor receptor (EGFR) signaling with GM3 ganglioside expression has been previously described. However, little is known about EGFR and NeuGcGM3 co-expression in cancer patients and their therapeutic implications. In this paper, we evaluate the co-expression of EGFR and NeuGcGM3 ganglioside in tumors from 92 patients and in two spontaneous lung metastasis models of mice (Lewis lung carcinoma (3LL-D122) in C57BL/6 and mammary carcinoma (4T1) in BALB/c). As results, co-expression of EGFR and NeuGcGM3 ganglioside was frequently observed in 63 of 92 patients (68 %), independently of histological subtype. Moreover, EGFR is co-expressed with NeuGcGM3 ganglioside in the metastasis of 3LL-D122 and 4T1 murine models. Such dual expression appears to be therapeutically relevant, since combined therapy with mAbs against these two molecules synergistically increase the survival of mice treated. Overall, our results suggest that NeuGcGM3 and EGFR may coordinately contribute to the tumor cell biology and that therapeutic combinations against these two targets might be a valid strategy to explore.

Indexed as

AnimalsAntibodies, MonoclonalCarcinoma, Lewis LungCell Line, TumorDisease Models, AnimalErbB ReceptorsFemaleGene Expression Regulation, NeoplasticG(M3) GangliosideHumansMammary Neoplasms, AnimalMiceNeoplasm MetastasisAntibodies, MonoclonalEGFR protein, mouseErbB ReceptorsG(M3) GangliosideN-glycolylneuraminyllactosylceramideCo-expressionCombination therapyEGFR, NeuGcGM3Pulmonary metastasis

Identifiers

PMID27449755
PMCPMC5035325
OpenAlexW2478796511

What OpenQuestion holds

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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.