Evidence map›Paper›PMID 29555893›Full record

ReviewMolecular cancer research : MCR2018

The Long (lncRNA) and Short (miRNA) of It: TGFβ-Mediated Control of RNA-Binding Proteins and Noncoding RNAs.

Harinarayanan Janakiraman, Reniqua P House, Vamsi K Gangaraju, J Alan Diehl, Philip H Howe, Viswanathan Palanisamy

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cancer research : MCR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 72 citations in OpenAlex.

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  12. Carcinogenic roles of MAFG-AS1 in human cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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  15. Long Noncoding RNAs in Taxane Resistance of Breast Cancer.International journal of molecular sciences · 2023
    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

6 authors at 1 institution in 1 country.

Harinarayanan Janakiraman *Department of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Reniqua P House *Department of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Vamsi K GangarajuDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina.
J Alan DiehlDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Philip H HoweDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Viswanathan PalanisamyDepartment of Biochemistry and Molecular Biology, College of Medicine, Medical University of South Carolina, Charleston, South Carolina. visu@musc.edu.
Medical University of South Carolina · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
TGF-regulated EMTR01CA154663 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Philip H Howe · 2011 to 2026
$5.1M
Mechanisms Of RNA-Binding Protein-Mediated Apoptosis In Oral MucositisR01DE022776 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PALANISAMY, VISWANATHAN · 2013 to 2017
$2.1M
Vascular and Neuronal Repair with Adipose Stromal Cells in RetinopathyR01EY023427 · NEI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GANGARAJU, RAJASHEKHAR · 2013 to 2017
$1.8M
Comprehensive Identification of FXR1 Targets Using pSILAC-BONCAT ProteomicsR21DE025920 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PALANISAMY, VISWANATHAN · 2017 to 2018
$411k
NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA154663NEI NIH HHS R01 EY023427NIDCR NIH HHS R01 DE022776NIDCR NIH HHS R21 DE025920
6 · The paper itself

Abstract

RNA-binding proteins (RBP) and noncoding RNAs (ncRNA), such as long noncoding RNAs (lncRNA) and microRNAs (miRNA), control co- and posttranscriptional gene regulation (PTR). At the PTR level, RBPs and ncRNAs contribute to pre-mRNA processing, mRNA maturation, transport, localization, turnover, and translation. Deregulation of RBPs and ncRNAs promotes the onset of cancer progression and metastasis. Both RBPs and ncRNAs are altered by signaling cascades to cooperate or compete with each other to bind their nucleic acid targets. Most importantly, transforming growth factor-beta (TGFβ) signaling plays a significant role in controlling gene expression patterns by targeting RBPs and ncRNAs. Because of TGFβ signaling in cancer, RBP-RNA or RNA-RNA interactions are altered and cause enhanced cell growth and tumor cell dissemination. This review focuses on the emerging concepts of TGFβ signaling on posttranscriptional gene regulation and highlights the implications of RBPs and ncRNAs in cancer progression and metastasis.

Indexed as

AnimalsDisease ProgressionGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm MetastasisNeoplasmsRNA-Binding ProteinsRNA, Long NoncodingRNA Processing, Post-TranscriptionalSignal TransductionTransforming Growth Factor betaMicroRNAsRNA-Binding ProteinsRNA, Long NoncodingTransforming Growth Factor beta

Identifiers

PMID29555893
PMCPMC6309266
OpenAlexW2790974348

What OpenQuestion holds

Textmetadata
LicenceTDM
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.