Evidence map›Paper›PMID 29435733›Full record

ArticlePathology oncology research : POR2020

Miki (Mitotic Kinetics Regulator) Immunoexpression in Normal Liver, Cirrhotic Areas and Hepatocellular Carcinomas: a Preliminary Study with Clinical Relevance.

Iván Fernández-Vega, Jorge Santos-Juanes, Emma Camacho-Urkaray, Laura Lorente-Gea, Beatriz García, Francisco Borja Gutiérrez-Corres, Luis M Quirós, Isabel Guerra-Merino, José Javier Aguirre

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In one paragraph

Article in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 99% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 1 country.

Iván Fernández-VegaDepartment of Pathology, Hospital Universitario de Araba-Txagorritxu, Vitoria-Gasteiz, Spain. ivan_fernandez_vega@hotmail.com.
Jorge Santos-JuanesDepartment of Pathology, Hospital Universitario Central de Asturias, Oviedo, Spain.
Emma Camacho-UrkarayDepartment of Pathology, Hospital Universitario de Araba-Txagorritxu, Vitoria-Gasteiz, Spain.
Laura Lorente-GeaDepartment of Pathology, Hospital Universitario de Araba-Txagorritxu, Vitoria-Gasteiz, Spain.
Beatriz GarcíaInstituto Universitario Fernández-Vega, Oviedo, Spain.
Francisco Borja Gutiérrez-CorresDepartment of Pathology, Hospital Universitario de Araba-Txagorritxu, Vitoria-Gasteiz, Spain.
Luis M QuirósInstituto Universitario Fernández-Vega, Oviedo, Spain.
Isabel Guerra-MerinoDepartment of Pathology, Hospital Universitario de Araba-Txagorritxu, Vitoria-Gasteiz, Spain.
José Javier AguirreDepartment of Pathology, Hospital Universitario de Araba-Txagorritxu, Vitoria-Gasteiz, Spain.
Hospital Txagorritxu · ESFernández-Vega Ophthalmological Institute · ESHospital Universitario Central de Asturias · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common type of primary malignant tumor in the liver. One of the main features of cancer survival is the generalized loss of growth control exhibited by cancer cells, and Miki is a protein related to the immunoglobulin superfamily that plays an important role in mitosis. We aim to study protein expression levels of Miki in non-tumoral liver and 20 HCCs recruited from a Pathology Department. Clinical information was also obtained. A tissue microarray was performed, and immunohistochemical techniques applied to study protein expression levels of Miki. In normal liver, Miki was weakly expressed, showing nuclear staining in the hepatocytes. Cirrhotic areas and HCCs showed a variety of staining patterns. Most HCC samples showed positive expression, with three different staining patterns being discernible: nuclear, cytoplasmic and mixed. Statistical analysis showed a significant association between grade of differentiation, Ki-67 proliferative index, survival rates and staining patterns. This study has revealed the positive expression of Miki in normal liver, cirrhotic areas and HCCs. Three different staining patterns of Miki expression with clinical relevance were noted in HCCs.

Indexed as

AgedAged, 80 and overCarcinoma, HepatocellularCell Cycle ProteinsCell NucleusCytoplasmFemaleHumansImmunohistochemistryKaplan-Meier EstimateKi-67 AntigenLiverLiver CirrhosisLiver NeoplasmsMaleMiddle AgedCell Cycle ProteinsHEPACAM2 protein, humanKi-67 AntigenHepatocellular carcinomaImmunoglobulin superfamilyImmunohistochemistryLiverMiki

Identifiers

PMID29435733
OpenAlexW2789057439

What Socratic 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 Socratic graph.