Evidence map›Paper›PMID 25842354›Full record

ArticleDigestive diseases and sciences2015

Differential Expression of Ion Channels and Transporters During Hepatocellular Carcinoma Development.

Violeta Zúñiga-García, María de Guadalupe Chávez-López, Valeria Quintanar-Jurado, Nayeli Belem Gabiño-López, Elisabeth Hernández-Gallegos, Juan Soriano-Rosas, Julio Isael Pérez-Carreón, Javier Camacho

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Article in Digestive diseases and sciences, 2015. 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
1.7field-weighted citation impact, top 16% 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, 33 citations in OpenAlex.

  1. Article
  2. Cannabidiol-Ion Channel Interactions Represent a Promising Preventive and Therapeutic Strategy in Hepatocellular Carcinoma.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
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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

8 authors at 4 institutions in 2 countries.

Violeta Zúñiga-GarcíaDepartment of Pharmacology, Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional, Avenida Instituto Politécnico Nacional 2508, C.P. 07360, Mexico City, Mexico, vzuniga@cinvestav.mx.
María de Guadalupe Chávez-López
Valeria Quintanar-Jurado
Nayeli Belem Gabiño-López
Elisabeth Hernández-Gallegos
Juan Soriano-Rosas
Julio Isael Pérez-Carreón
Javier Camacho
Instituto Politécnico Nacional · MXNational Institute of Genomic Medicine · MXHospital General de México · MXInstituto de Medicina Genómica · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIon channels and transporters are potential markers and therapeutic targets for several cancers. However, their expression during hepatocellular carcinoma (HCC) development remains unclear.

aimTo investigate the mRNA expression of Na(+), K(+) and Ca(2+) channels and ABC transporters during rat HCC development, as well as Abcc3 protein in human liver biopsies.

methodsWistar rats were treated with diethylnitrosamine (DEN) and developed both cirrhosis (12 weeks of treatment) and either pre-neoplastic lesions (16 weeks of treatment) or multinodular HCC (16 weeks of treatment plus 2 weeks DEN-free). The mRNA expression of 12 ion channels and two ABC transporters was studied using real-time RT-PCR. Tumor-containing or tumor-free liver sections were isolated by laser-capture microdissection. Abcc3 protein expression was studied by immunohistochemistry in healthy, cirrhotic and HCC human biopsies.

resultsWe observed expression changes in seven genes. Kcna3, Kcnn4, Kcnrg and Kcnj11 potassium channel mRNA expression reached peak values at the end of DEN treatment, while Scn2a1 sodium channel, Trpc6 calcium channel and Abcc3 transporter mRNA expression reached their highest levels in the presence of HCC (18 weeks). Whereas Kcnn4 and Scn2a1 channel expression was similar in non-tumor and tumor tissue, the Abcc3 transporter and Kcna3 potassium channels were preferentially overexpressed in the tumor sections. We observed differential Abcc3 protein subcellular localization and expression in human samples.

conclusionsThe ion channel/transporter expression profile observed suggests that these genes are potential early markers or therapeutic targets of HCC. The differential localization of Abcc3 may be useful in the diagnosis of cirrhosis and HCC.

Indexed as

AnimalsATP-Binding Cassette, Sub-Family C ProteinsCalcium ChannelsCarcinoma, HepatocellularHumansImmunohistochemistryIon ChannelsLaser Capture MicrodissectionLiver NeoplasmsMalePotassium ChannelsRats, WistarReal-Time Polymerase Chain ReactionSodium ChannelsATP-Binding Cassette, Sub-Family C ProteinsCalcium ChannelsIon Channelsmultidrug resistance-associated protein 3Potassium ChannelsSodium Channels

Identifiers

PMID25842354
OpenAlexW2002151182

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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.