Evidence map›Paper›PMID 30857150›Full record

ArticleInternational journal of molecular sciences2019

Temporal Splicing Switches in Elements of the TNF-Pathway Identified by Computational Analysis of Transcriptome Data for Human Cell Lines.

Nikolai Genov, Alireza Basti, Mónica Abreu, Angela Relógio

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 8 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

4 authors at 1 institution in 1 country.

Nikolai GenovCharité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Theoretical Biology, 10115 Berlin, Germany. nikolai.genov@zedat.fu-berlin.de.
Alireza BastiCharité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Theoretical Biology, 10115 Berlin, Germany. alireza.basti@charite.de.ORCID 0000-0002-0153-2784
Mónica AbreuCharité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Theoretical Biology, 10115 Berlin, Germany. monica_tpa@live.com.pt.ORCID 0000-0003-0626-7999
Angela RelógioCharité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Theoretical Biology, 10115 Berlin, Germany. angela.relogio@charite.de.
Humboldt-Universität zu Berlin · DE

Funding

Dr. Rolf M. Schwiete Stiftung 09/2017German Federal Ministry of Education and Research (BMBF) eBio-CIRSPLICE-FKZ031A316
6 · The paper itself

Abstract

Alternative splicing plays an important role in numerous cellular processes and aberrant splice decisions are associated with cancer. Although some studies point to a regulation of alternative splicing and its effector mechanisms in a time-dependent manner, the extent and consequences of such a regulation remains poorly understood. In the present work, we investigated the time-dependent production of isoforms in two Hodgkin lymphoma cell lines of different progression stages (HD-MY-Z, stage IIIb and L-1236, stage IV) compared to a B lymphoblastoid cell line (LCL-HO) with a focus on tumour necrosis factor (TNF) pathway-related elements. For this, we used newly generated time-course RNA-sequencing data from the mentioned cell lines and applied a computational pipeline to identify genes with isoform-switching behaviour in time. We analysed the temporal profiles of the identified events and evaluated in detail the potential functional implications of alterations in isoform expression for the selected top-switching genes. Our data indicate that elements within the TNF pathway undergo a time-dependent variation in isoform production with a putative impact on cell migration, proliferation and apoptosis. These include the genes

Indexed as

Alternative SplicingSignal TransductionTranscriptomeCell Line, TumorCell MovementCell ProliferationCircadian ClocksHodgkin DiseaseHumansProtein IsoformsRNASequence Analysis, RNATumor Necrosis Factor-alphaProtein IsoformsRNATumor Necrosis Factor-alphaalternative splicinganalysis of oscillating genescancercircadian clockhigh-throughput data analysispathway enrichmentRNA-sequencingsystems biologyTNF-pathway

Identifiers

PMID30857150
PMCPMC6429354
OpenAlexW2918708422

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.