Evidence map›Paper›PMID 26337276›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

The transmembrane transporter ABCC3 participates in liver cancer progression and is a potential biomarker.

Gabriela Carrasco-Torres, Samia Fattel-Fazenda, Guadalupe Soledad López-Alvarez, Rebeca García-Román, Saúl Villa-Treviño, Verónica Rocío Vásquez-Garzón

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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  7. Protein expression and function of organic anion transporters in short-term and long-term cultures of Huh7 human hepatoma cells.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2019
    Article
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

6 authors at 3 institutions in 1 country.

Gabriela Carrasco-TorresDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN (CINVESTAV), México D.F., Mexico.
Samia Fattel-FazendaDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN (CINVESTAV), México D.F., Mexico.
Guadalupe Soledad López-AlvarezDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN (CINVESTAV), México D.F., Mexico.
Rebeca García-RománInstituto de Salud Pública, Universidad Veracruzana, Veracruz, Mexico.
Saúl Villa-TreviñoDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN (CINVESTAV), México D.F., Mexico. svilla@cell.cinvestav.mx.
Verónica Rocío Vásquez-GarzónDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN (CINVESTAV), México D.F., Mexico. vrvasquezga@conacyt.mx.
Center for Research and Advanced Studies of the National Polytechnic Institute · MXBenito Juárez Autonomous University of Oaxaca · MXUniversidad Veracruzana · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The poor prognosis, few available treatment options, and multidrug resistance present in hepatocellular carcinoma are major problems, and new early biomarkers are needed to reduce the liver cancer death rate. ATP-binding cassette sub-family C member 3 (Abcc3) is overexpressed in different cancers and is associated with multidrug resistance and a carcinogenic stem cell phenotype. We present evidence for the first time that ABCC3 is a potential sanguine biomarker and anticancer target in hepatocellular carcinoma. Abcc3 mRNA expression was elevated in liver nodules and tumors in rat hepatocarcinogenesis model. Accordingly, the ABCC3 protein was preferentially overexpressed within the nodules and tumors during hepatocellular carcinoma progression and was secreted into the bloodstream of rat hepatocarcinogenesis model. The ABCC3 protein was expressed in human hepatoma cells and, importantly, was also present in HepG2- and Huh7-conditioned media. Furthermore, ABCC3 was overexpressed in human hepatocellular carcinoma. This report is the first to describe liver overexpression of Abcc3 during the cancer initiation, promotion, and progression periods in rat hepatocarcinogenesis model and in human hepatocellular carcinoma.

Indexed as

AnimalsATP-Binding Cassette, Sub-Family C ProteinsBiomarkers, TumorBlotting, WesternCarcinoma, HepatocellularDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHumansImmunohistochemistryLiver NeoplasmsMaleRatsRats, Inbred F344Real-Time Polymerase Chain ReactionTranscriptomeATP-Binding Cassette, Sub-Family C ProteinsBiomarkers, Tumormultidrug resistance-associated protein 3ABCC3BiomarkerLiver cancerPlasma

Identifiers

PMID26337276
OpenAlexW1782342531

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.