Evidence map›Paper›PMID 29227193›Full record

ArticleRNA biology2018

DDX5/p68 associated lncRNA LOC284454 is differentially expressed in human cancers and modulates gene expression.

Monalisa Das, Arun Renganathan, Shrinivas Nivrutti Dighe, Utsa Bhaduri, Abhijith Shettar, Geetashree Mukherjee, Paturu Kondaiah, Manchanahalli R Satyanarayana Rao

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  8. Long non-coding RNAs: From disease code to drug role.Acta pharmaceutica Sinica. B · 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

8 authors at 3 institutions in 1 country.

Monalisa Dasa Molecular Biology and Genetics Unit , Jawaharlal Nehru Centre for Advance Scientific Research , Bangalore , Karnataka , India.
Arun Renganathana Molecular Biology and Genetics Unit , Jawaharlal Nehru Centre for Advance Scientific Research , Bangalore , Karnataka , India.ORCID 0000-0002-6722-8136
Shrinivas Nivrutti Dighea Molecular Biology and Genetics Unit , Jawaharlal Nehru Centre for Advance Scientific Research , Bangalore , Karnataka , India.
Utsa Bhaduria Molecular Biology and Genetics Unit , Jawaharlal Nehru Centre for Advance Scientific Research , Bangalore , Karnataka , India.
Abhijith Shettarb Molecular Reproduction, Development and Genetics , Indian Institute of Science , Bangalore , Karnataka , India.
Geetashree Mukherjeec Kidwai Memorial Institute of Oncology , Bangalore , Karnataka , India.
Paturu Kondaiahb Molecular Reproduction, Development and Genetics , Indian Institute of Science , Bangalore , Karnataka , India.
Manchanahalli R Satyanarayana Raoa Molecular Biology and Genetics Unit , Jawaharlal Nehru Centre for Advance Scientific Research , Bangalore , Karnataka , India.
Jawaharlal Nehru Centre for Advanced Scientific Research · INIndian Institute of Science Bangalore · INKidwai Memorial Institute of Oncology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) are emerging as important players in regulation of gene expression in higher eukaryotes. DDX5/p68 RNA helicase protein which is involved in splicing of precursor mRNAs also interacts with lncRNAs like, SRA and mrhl, to modulate gene expression. We performed RIP-seq analysis in HEK293T cells to identify the complete repertoire of DDX5/p68 interacting transcripts including 73 single exonic (SE) lncRNAs. The LOC284454 lncRNA is the second top hit of the list of SE lncRNAs which we have characterized in detail for its molecular features and cellular functions. The RNA is located in the same primary transcript harboring miR-23a∼27a∼24-2 cluster. LOC284454 is a stable, nuclear restricted and chromatin associated lncRNA. The sequence is conserved only in primates among 26 different species and is expressed in multiple human tissues. Expression of LOC284454 is significantly reduced in breast, prostate, uterus and kidney cancer and also in breast cancer cell lines (MCF7 and T47D). Global gene expression studies upon loss and gain of function of LOC284454 revealed perturbation of genes related to cancer-related pathways. Focal adhesion and cell migration pathway genes are downregulated under overexpression condition, and these genes are significantly upregulated in breast cancer cell lines as well as breast cancer tissue samples suggesting a functional role of LOC284454 lncRNA in breast cancer pathobiology.

Indexed as

Cell Line, TumorDEAD-box RNA HelicasesDown-RegulationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHEK293 CellsHumansMaleMCF-7 CellsNeoplasmsOligonucleotide Array Sequence AnalysisRNA, Long NoncodingSequence Analysis, RNASignal TransductionDdx5 protein, humanDEAD-box RNA HelicasesRNA, Long NoncodingCancerDDX5/p68 RNA helicasegene expressionLOC284454Long non-coding RNA

Identifiers

PMID29227193
PMCPMC5798960
OpenAlexW2772390408

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Registered trials

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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.