Evidence map›Paper›PMID 32825637›Full record

ArticleInternational journal of molecular sciences2020

Remodeling of Kv7.1 and Kv7.5 Expression in Vascular Tumors.

Clara Serrano-Novillo, Anna Oliveras, Joan Carles Ferreres, Enric Condom, Antonio Felipe

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Voltage-Gated Potassium Channels as Regulators of Cell Death.Frontiers in cell and developmental biology · 2020
    Review
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

5 authors at 3 institutions in 1 country.

Clara Serrano-NovilloMolecular Physiology Laboratory, Department de Bioquímica i Biomedicina Molecular, Institut de Biomedicina (IBUB), Universitat de Barcelona, 08028 Barcelona, Spain.
Anna OliverasMolecular Physiology Laboratory, Department de Bioquímica i Biomedicina Molecular, Institut de Biomedicina (IBUB), Universitat de Barcelona, 08028 Barcelona, Spain.ORCID 0000-0002-5880-5245
Joan Carles FerreresConsorci Corporació Sanitària Parc Taulí-Parc Taulí Hospital Universitari, Universitat Autónoma de Barcelona, 08208 Sabadell, Spain.ORCID 0000-0001-7742-0239
Enric CondomInstitut d'Investigació Biomèdica de Bellvitge (IDIBELL), Hospital Universitari de Bellvitge, 08907 L'Hospitalet de Llobregat, Spain.ORCID 0000-0003-0142-3729
Antonio FelipeMolecular Physiology Laboratory, Department de Bioquímica i Biomedicina Molecular, Institut de Biomedicina (IBUB), Universitat de Barcelona, 08028 Barcelona, Spain.ORCID 0000-0002-7294-6431
Universitat de Barcelona · ESBellvitge University Hospital · ESUniversitat Autònoma de Barcelona · ES

Funding

European Regional Development Fund BFU2017-87104-RMinisterio de Economía, Industria y Competitividad, Gobierno de España BFU2017-87104-R
6 · The paper itself

Abstract

Voltage-dependent potassium (Kv) channels contribute to the excitability of nerves and muscles. In addition, Kv participates in several cell functions, including cell cycle progression and proliferation. Kv channel remodeling has been associated with neoplastic cell growth and cancer. Kv7 channels are expressed in blood vessels, and they participate in the maintenance of vascular tone and are implicated in myocyte proliferation. Although evidence links Kv7 remodeling to different types of cancer, its expression in vascular tumors has never been studied. Endothelium-derived vascular neoplasms range from indolent lesions to highly aggressive and metastasizing cancers. Here, we show that Kv7.1 and Kv7.5 are evenly distributed in tunicas as well as the endothelium of healthy veins and arteries. The layered structure of vessels is lost in vascular tumors. By studying eight vascular tumors with different origins and characteristics, we found that Kv7.1 and Kv7.5 expression was changed in vascular cancers. While both channels were generally downregulated, Kv7.5 expression was clearly correlated with neoplastic malignancy. The vascular tumors did not contract; therefore, the role of Kv7 channels is probably related to proliferation rather than controlling vascular tone. Our results identify vascular Kv7 channels as targets for cancer detection and anticancer therapies.

Indexed as

AnimalsArteriesBiomarkers, TumorHumansKCNQ1 Potassium ChannelKCNQ Potassium ChannelsMicroscopy, ConfocalRatsVascular NeoplasmsBiomarkers, TumorKCNQ1 Potassium ChannelKCNQ1 protein, humanKCNQ5 protein, humanKcnq5 protein, ratKCNQ Potassium Channelsblood vesselscancerneoplasiapotassium channels

Identifiers

PMID32825637
PMCPMC7503939
OpenAlexW3080308015

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.