Evidence map›Paper›PMID 29165391›Full record

ReviewInternational journal of molecular sciences2017

MicroRNAs Associated with Von Hippel-Lindau Pathway in Renal Cell Carcinoma: A Comprehensive Review.

Lisa-Maria Schanza, Maximilian Seles, Michael Stotz, Johannes Fosselteder, Georg C Hutterer, Martin Pichler, Verena Stiegelbauer

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  13. Non-Coding RNAs in Hereditary Kidney Disorders.International journal of molecular sciences · 2021
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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

7 authors at 2 institutions in 2 countries.

Lisa-Maria SchanzaDivision of Oncology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria. Lisa-Maria.Schanza@klinikum-graz.at.
Maximilian SelesDepartment of Urology, Medical University of Graz, 8036 Graz, Austria. maximilian.seles@medunigraz.at.
Michael StotzDivision of Oncology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria. michael.stotz@klinikum-graz.at.
Johannes FosseltederDivision of Oncology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria. johannes.fosselteder@edu.uni-graz.at.
Georg C HuttererDepartment of Urology, Medical University of Graz, 8036 Graz, Austria. georg.hutterer@medunigraz.at.
Martin PichlerDivision of Oncology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria. martin.pichler@medunigraz.at.
Verena StiegelbauerResearch Unit of Non-Coding RNA and Genome Editing in Cancer, Division of Oncology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria. verena.stiegelbauer@medunigraz.at.
Medical University of Graz · ATThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) are the most common renal neoplasia and can be divided into three main histologic subtypes, among which clear cell RCC is by far the most common form of kidney cancer. Despite substantial advances over the last decade in the understanding of RCC biology, surgical treatments, and targeted and immuno-therapies in the metastatic setting, the prognosis for advanced RCC patients remains poor. One of the major problems with RCC treatment strategies is inherent or acquired resistance towards therapeutic agents over time. The discovery of microRNAs (miRNAs), a class of small, non-coding, single-stranded RNAs that play a crucial role in post-transcriptional regulation, has added new dimensions to the development of novel diagnostic and treatment tools. Because of an association between Von Hippel-Lindau (VHL) genes with chromosomal loss in 3p25-26 and clear cell RCC, miRNAs have attracted considerable scientific interest over the last years. The loss of VHL function leads to constitutional activation of the hypoxia inducible factor (HIF) pathway and to consequent expression of numerous angiogenic and carcinogenic factors. Since miRNAs represent key players of carcinogenesis, tumor cell invasion, angiogenesis, as well as in development of metastases in RCC, they might serve as potential therapeutic targets. Several miRNAs are already known to be dysregulated in RCC and have been linked to biological processes involved in tumor angiogenesis and response to anti-cancer therapies. This review summarizes the role of different miRNAs in RCC angiogenesis and their association with the VHL gene, highlighting their potential role as novel drug targets.

Indexed as

Signal TransductionAngiogenesis InhibitorsAnimalsAntineoplastic AgentsCarcinoma, Renal CellGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1Kidney NeoplasmsMicroRNAsMolecular Targeted TherapyNeovascularization, PathologicVon Hippel-Lindau Tumor Suppressor ProteinAngiogenesis InhibitorsAntineoplastic AgentsHypoxia-Inducible Factor 1MicroRNAsVon Hippel-Lindau Tumor Suppressor ProteinangiogenesismicroRNAsrenal cell carcinomaVon Hippel-Lindau

Identifiers

PMID29165391
PMCPMC5713461
OpenAlexW2768713849

What OpenQuestion 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 OpenQuestion graph.