Evidence map›Paper›PMID 28652429›Full record

ArticleIn vivo (Athens, Greece)

MicroRNA-1 and MicroRNA-21 Individually Regulate Cellular Growth of Non-malignant and Malignant Renal Cells.

Hannes Ahrend, Anne Kaul, Susanne Ziegler, Lars-Ove Brandenburg, Uwe Zimmermann, Alexander Mustea, Martin Burchardt, Patrick Ziegler, Matthias B Stope

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. MicroRNAs: The Link between the Metabolic Syndrome and Oncogenesis.International journal of molecular sciences · 2021
    Review
  3. [Comprehensive analysis of the aberrantly expressed profiles of lncRNAs, miRNAs and the regulation network of the associated ceRNAs in clear cell renal cell carcinoma].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2019
    Article
  4. Article
  5. Determination ofIn vivo (Athens, Greece)
    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 2 institutions in 1 country.

Hannes AhrendDepartment of Urology, University of Medicine Greifswald, Greifswald, Germany.
Anne KaulDepartment of Gynaecology and Obstetrics, University of Medicine Greifswald, Greifswald, Germany.
Susanne ZieglerInstitute for Occupational and Social Medicine, RWTH Aachen University, Aachen, Germany.
Lars-Ove BrandenburgDepartment of Anatomy and Cell Biology, RWTH Aachen University, Aachen, Germany.
Uwe ZimmermannDepartment of Urology, University of Medicine Greifswald, Greifswald, Germany.
Alexander MusteaDepartment of Gynaecology and Obstetrics, University of Medicine Greifswald, Greifswald, Germany.
Martin BurchardtDepartment of Urology, University of Medicine Greifswald, Greifswald, Germany.
Patrick ZieglerInstitute for Occupational and Social Medicine, RWTH Aachen University, Aachen, Germany.
Matthias B StopeDepartment of Urology, University of Medicine Greifswald, Greifswald, Germany matthias.stope@uni-greifswald.de.
Universitätsmedizin Greifswald · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimDue to its poor prognosis, it is increasingly necessary to understand the biology of renal cell cancer (RCC). Therefore, we investigated the role of microRNAs miR-1 and miR-21 in the growth of RCC cells compared to that of non-malignant renal cells. MATERIALS AND

methodsFour malignant cell lines (Caki-1, 786-O, RCC4, A498) were examined regarding their cell growth, microRNA and telomerase expression, and were compared to non-malignant RC-124 renal cells.

resultsInconsistencies appeared in the panel of RCC cells regarding antiproliferative and proliferative properties of miR-1 and miR-21, respectively. Notably, and most likely due to immortaliziation, non-malignant RC-124 cells exhibited telomerase expression and activity.

conclusionmiR-1 and miR-21 functionality in cancer progression, particularly in tumor growth, may be more dependent on the individual cellular context and may reflect RCC heterogeneity. Thus, both microRNAs, in combination with other stratifying biomarkers, may be useful in terms of RCC diagnosis, prognosis, or treatment response.

Indexed as

CarcinogenesisCarcinoma, Renal CellCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansKidneyMicroRNAsNeoplasm InvasivenessTelomeraseMicroRNAsMIRN1 microRNA, humanMIRN21 microRNA, humanTelomerasemicroRNA-1microRNA-21proliferationRenal cell carcinoma

Identifiers

PMID28652429
PMCPMC5566912
OpenAlexW2663104430

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.