Evidence map›Paper›PMID 31817194›Full record

ArticleCancers2019

CTCs Expression Profiling for Advanced Breast Cancer Monitoring.

Thais Pereira-Veiga, Mónica Martínez-Fernández, Carmen Abuin, Roberto Piñeiro, Victor Cebey, Juan Cueva, Patricia Palacios, Cristina Blanco, Laura Muinelo-Romay, Alicia Abalo and 2 more

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
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  10. miR-205-5p Downregulation andInternational journal of molecular sciences · 2021
    Article
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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.

Thais Pereira-VeigaRoche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela, Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain.ORCID 0000-0002-4473-7608
Mónica Martínez-FernándezGenomes and Disease Lab, CIMUS-Molecular Medicine and Chronic Diseases Research Centre, Universidade de Santiago de Compostela, Avda Barcelona s/n, 15706 Santiago de Compostela, Spain.
Carmen AbuinRoche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela, Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain.ORCID 0000-0002-6902-4161
Roberto PiñeiroRoche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela, Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain.
Victor CebeyDepartment of Oncology, Complexo Hospitalario Universitario de Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain.
Juan CuevaDepartment of Oncology, Complexo Hospitalario Universitario de Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain.
Patricia PalaciosDepartment of Oncology, Complexo Hospitalario Universitario de Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain.
Cristina BlancoDepartment of Oncology, Complexo Hospitalario Universitario de Santiago de Compostela (SERGAS), 15706 Santiago de Compostela, Spain.
Laura Muinelo-RomayCIBERONC, Centro de Investigación Biomédica en Red Cáncer, 28029 Madrid, Spain.ORCID 0000-0002-7456-7531
Alicia AbaloLiquid Biopsy Analysis Unit, Translational Medical Oncology Group, Health Research Institute of Santiago, de Santiago de Compostela (SERGAS), Trav. Choupana s/n, 15706 Santiago de Compostela, Spain.
Clotilde CostaRoche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela, Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain.ORCID 0000-0001-7327-2259
Rafael López-LópezRoche-Chus Joint Unit, Translational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela, Travesía da Choupana s/n, 15706 Santiago de Compostela, Spain.

Funding

Consellería de Economía, Emprego e Industria, Xunta de Galicia Roche-Chus Joint Unit (IN853B 2018/03)
6 · The paper itself

Abstract

The study of circulating tumor cells (CTCs) has a huge clinical interest in advance and metastatic breast cancer patients. However, many approaches are biased by the use of epithelial markers, which underestimate non-epithelial CTCs phenotypes. CTCs enumeration provides valuable prognostic information; however, molecular characterization could be the best option to monitor patients throughout the disease since it may provide more relevant clinical information to the physicians. In this work, we aimed at enumerating and performing a molecular characterization of CTCs from a cohort of 20 patients with metastatic breast cancer (MBC), monitoring the disease at different time points of the therapy, and at progression when it occurred. To this end, we used a CTC negative enrichment protocol that allowed us to recover a higher variety of CTCs phenotypes. With this strategy, we were able to obtain gene expression data from CTCs from all the patients. In addition, we found that high expression levels of

Indexed as

breast cancerCTCsgene expressionmetastasismolecular/gene signaturepredictive biomarkers

Identifiers

PMID31817194
PMCPMC6966538

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.