Evidence map›Paper›PMID 27725909›Full record

ArticleAmerican journal of cancer research2016

Cell cycle dependent RRM2 may serve as proliferation marker and pharmaceutical target in adrenocortical cancer.

Vince Kornél Grolmusz, Katalin Karászi, Tamás Micsik, Eszter Angéla Tóth, Katalin Mészáros, Gellért Karvaly, Gábor Barna, Péter Márton Szabó, Kornélia Baghy, János Matkó and 5 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  4. Sex differences in human pre-gastrulation embryos.Science China. Life sciences · 2025
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  11. GINS2 promotes the progression of human HNSCC by altering RRM2 expression.Cancer biomarkers : section A of Disease markers · 2024
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  17. Review
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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

15 authors at 3 institutions in 1 country.

Vince Kornél Grolmusz2nd Department of Medicine, Semmelweis UniversityBudapest, Hungary; "Lendület" Hereditary Endocrine Tumours Research Group, Hungarian Academy of Sciences, Semmelweis UniversityBudapest, Hungary.
Katalin Karászi1st Department of Pathology and Experimental Cancer Research, Semmelweis University Budapest, Hungary.
Tamás Micsik1st Department of Pathology and Experimental Cancer Research, Semmelweis University Budapest, Hungary.
Eszter Angéla TóthDepartment of Immunology, Eötvös Loránd University Budapest, Hungary.
Katalin Mészáros"Lendület" Hereditary Endocrine Tumours Research Group, Hungarian Academy of Sciences, Semmelweis UniversityBudapest, Hungary; Department of Laboratory Medicine, Semmelweis UniversityBudapest, Hungary.
Gellért Karvaly"Lendület" Hereditary Endocrine Tumours Research Group, Hungarian Academy of Sciences, Semmelweis UniversityBudapest, Hungary; Department of Laboratory Medicine, Semmelweis UniversityBudapest, Hungary; Bionics Innovation CenterBudapest, Hungary.
Gábor Barna1st Department of Pathology and Experimental Cancer Research, Semmelweis University Budapest, Hungary.
Péter Márton SzabóMolecular Medicine Research Group, Hungarian Academy of Sciences, Semmelweis University Budapest, Hungary.
Kornélia Baghy1st Department of Pathology and Experimental Cancer Research, Semmelweis University Budapest, Hungary.
János MatkóDepartment of Immunology, Eötvös Loránd University Budapest, Hungary.
Ilona Kovalszky1st Department of Pathology and Experimental Cancer Research, Semmelweis University Budapest, Hungary.
Miklós Tóth2nd Department of Medicine, Semmelweis University Budapest, Hungary.
Károly Rácz2nd Department of Medicine, Semmelweis UniversityBudapest, Hungary; Molecular Medicine Research Group, Hungarian Academy of Sciences, Semmelweis UniversityBudapest, Hungary.
Péter Igaz2nd Department of Medicine, Semmelweis University Budapest, Hungary.
Attila Patócs"Lendület" Hereditary Endocrine Tumours Research Group, Hungarian Academy of Sciences, Semmelweis UniversityBudapest, Hungary; Department of Laboratory Medicine, Semmelweis UniversityBudapest, Hungary; Bionics Innovation CenterBudapest, Hungary.
Semmelweis University · HUEötvös Loránd University · HUHungarian Academy of Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adrenocortical cancer (ACC) is a rare, but agressive malignancy with poor prognosis. Histopathological diagnosis is challenging and pharmacological options for treatment are limited. By the comparative reanalysis of the transcriptional malignancy signature with the cell cycle dependent transcriptional program of ACC, we aimed to identify novel biomarkers which may be used in the histopathological diagnosis and for the prediction of therapeutical response of ACC. Comparative reanalysis of publicly available microarray datasets included three earlier studies comparing transcriptional differences between ACC and benign adrenocortical adenoma (ACA) and one study presenting the cell cycle dependent gene expressional program of human ACC cell line NCI-H295R. Immunohistochemical analysis was performed on ACC samples.

Indexed as

adrenocortical cancer (ACC)cell cyclecell cycle-dependentchemoresistanceFluorescence activated cell sorting (FACS)gemcitabine-resistancemalignancy signatureproliferation markerribonucleotide reductaseribonucleotide reductase subunit 2 (RRM2)

Identifiers

PMID27725909
PMCPMC5043113
OpenAlexW2556631593

What OpenQuestion holds

Textmetadata
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.