Evidence map›Paper›PMID 34681854›Full record

ReviewInternational journal of molecular sciences2021

LncRNAs in the Regulation of Genes and Signaling Pathways through miRNA-Mediated and Other Mechanisms in Clear Cell Renal Cell Carcinoma.

Eleonora A Braga, Marina V Fridman, Elena A Filippova, Vitaly I Loginov, Irina V Pronina, Alexey M Burdennyy, Alexander V Karpukhin, Alexey A Dmitriev, Sergey G Morozov

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Eleonora A BragaInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID 0000-0001-5188-4094
Marina V FridmanVavilov Institute of General Genetics, Russian Academy of Sciences, 119991 Moscow, Russia.
Elena A FilippovaInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Vitaly I LoginovInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Irina V ProninaInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Alexey M BurdennyyInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID 0000-0002-9398-8075
Alexander V KarpukhinResearch Centre for Medical Genetics, 115522 Moscow, Russia.
Alexey A DmitrievEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-6827-9584
Sergey G MorozovInstitute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Research Institute of General Pathology and Pathophysiology, the Russian Academy of Medical Sciences · RUEngelhardt Institute of Molecular Biology · RUResearch Centre for Medical Genetics · RUVavilov Institute of General Genetics · RU

Funding

Ministry of Science and Higher Education of the Russian Federation state assignment for 2019-2021
6 · The paper itself

Abstract

The fundamental novelty in the pathogenesis of renal cell carcinoma (RCC) was discovered as a result of the recent identification of the role of long non-coding RNAs (lncRNAs). Here, we discuss several mechanisms for the dysregulation of the expression of protein-coding genes initiated by lncRNAs in the most common and aggressive type of kidney cancer-clear cell RCC (ccRCC). A model of competitive endogenous RNA (ceRNA) is considered, in which lncRNA acts on genes through the lncRNA/miRNA/mRNA axis. For the most studied oncogenic lncRNAs, such as HOTAIR, MALAT1, and TUG1, several regulatory axes were identified in ccRCC, demonstrating a number of sites for various miRNAs. Interestingly, the LINC00973/miR-7109/Siglec-15 axis represents a novel agent that can suppress the immune response in patients with ccRCC, serving as a valuable target in addition to the PD1/PD-L1 pathway. Other mechanisms of action of lncRNAs in ccRCC, involving direct binding with proteins, mRNAs, and genes/DNA, are also considered. Our review briefly highlights methods by which various mechanisms of action of lncRNAs were verified. We pay special attention to protein targets and signaling pathways with which lncRNAs are associated in ccRCC. Thus, these new data on the different mechanisms of lncRNA functioning provide a novel basis for understanding the pathogenesis of ccRCC and the identification of new prognostic markers and targets for therapy.

Indexed as

Gene Expression Regulation, NeoplasticSignal TransductionCarcinoma, Renal CellHumansKidney NeoplasmsRNA, Long NoncodingRNA, Long Noncodingalternative mechanismsclear cell renal cell carcinomacompetitive endogenous RNA modellncRNAprotein targets and signaling pathways

Identifiers

PMID34681854
PMCPMC8539140
OpenAlexW3207706894

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.