Evidence map›Paper›PMID 34071030›Full record

ArticleCancers2021

Possible Role of IRS-4 in the Origin of Multifocal Hepatocellular Carcinoma.

Luis G Guijarro, Patricia Sanmartin-Salinas, Eva Pérez-Cuevas, M Val Toledo-Lobo, Jorge Monserrat, Sofía Zoullas, Miguel A Sáez, Miguel A Álvarez-Mon, Julia Bujan, Fernando Noguerales-Fraguas and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Pathogenetic Dichotomy in Angioleiomyoma.Cancer genomics & proteomics
    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

13 authors at 1 institution in 1 country.

Luis G GuijarroUnit of Biochemistry and Molecular Biology (CIBEREHD), Department of System Biology, University of Alcalá, 28801 Alcala de Henares, Spain.
Patricia Sanmartin-SalinasUnit of Biochemistry and Molecular Biology (CIBEREHD), Department of System Biology, University of Alcalá, 28801 Alcala de Henares, Spain.
Eva Pérez-CuevasUnit of Biochemistry and Molecular Biology (CIBEREHD), Department of System Biology, University of Alcalá, 28801 Alcala de Henares, Spain.ORCID 0000-0001-6477-1283
M Val Toledo-LoboUnit of Cell Biology, Department of Biomedicine and Biotechnology, University of Alcala, 28871 Alcala de Henares, Spain.
Jorge MonserratRamón y Cajal Institute of Sanitary Research (IRYCIS), 28034 Madrid, Spain.ORCID 0000-0003-1775-4645
Sofía ZoullasDepartment of Medicine and Medical Specialities, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcala de Henares, Spain.
Miguel A SáezDepartment of Medicine and Medical Specialities, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcala de Henares, Spain.ORCID 0000-0002-8389-258X
Miguel A Álvarez-MonRamón y Cajal Institute of Sanitary Research (IRYCIS), 28034 Madrid, Spain.
Julia BujanRamón y Cajal Institute of Sanitary Research (IRYCIS), 28034 Madrid, Spain.ORCID 0000-0003-2419-2476
Fernando Noguerales-FraguasDepartment of Surgery, Medical and Social Sciences, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcala de Henares, Spain.
Eduardo Arilla-FerreiroUnit of Biochemistry and Molecular Biology (CIBEREHD), Department of System Biology, University of Alcalá, 28801 Alcala de Henares, Spain.
Melchor Álvarez-MonRamón y Cajal Institute of Sanitary Research (IRYCIS), 28034 Madrid, Spain.
Miguel A OrtegaRamón y Cajal Institute of Sanitary Research (IRYCIS), 28034 Madrid, Spain.ORCID 0000-0003-2588-1708
Universidad de Alcalá · ES

Funding

METHADONE TREATMENT: A STUDY OF A COUNTY POLICY CHANGER01DA003804 · NIDA · SCIENTIFIC ANALYSIS CORPORATION · PI ROSENBAUM, MARSHA · 1985 to 1989
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Comunidad de Madrid B2017/BMD-3804 MITIC-CMUniversidad de Alcalá 32/2013, 22/2014, 26/2015
6 · The paper itself

Abstract

New evidence suggests that insulin receptor substrate 4 (IRS-4) may play an important role in the promotion of tumoral growth. In this investigation, we have evaluated the role of IRS-4 in a pilot study performed on patients with liver cancer. We used immunohistochemistry to examine IRS-4 expression in biopsies of tumoral tissue from a cohort of 31 patient suffering of hepatocellular carcinoma (HCC). We simultaneously analyzed the expression of the cancer biomarkers PCNA, Ki-67, and pH3 in the same tissue samples. The in vitro analysis was conducted by studying the behavior of HepG2 cells following IRS-4 overexpression/silencing. IRS-4 was expressed mainly in the nuclei of tumoral cells from HCC patients. In contrast, in healthy cells involved in portal triads, canaliculi, and parenchymal tissue, IRS-4 was observed in the cytosol and the membrane. Nuclear IRS-4 in the tumoral region was found in 69.9 ± 3.2%, whereas in the surrounding healthy hepatocytes, nuclear IRS-4 was rarely observed. The percentage of tumoral cells that exhibited nuclear PCNA and Ki-67 were 52.1 ± 7%, 6.1 ± 1.1% and 1.3 ± 0.2%, respectively. Furthermore, we observed a significant positive linear correlation between nuclear IRS-4 and PCNA (r = 0.989;

Indexed as

cyclin Dhepatocellular carcinomaintegrin α2/β1 and FAKnuclear IRS-4PI3Kβ-catenin

Identifiers

PMID34071030
PMCPMC8197110
OpenAlexW3165881150

What Socratic 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 Socratic graph.