Evidence map›Paper›PMID 29113151›Full record

ArticleOncology letters2017

Alternative splicing regulation in tumor necrosis factor-mediated inflammation.

Eduardo López-Urrutia, Alma Campos-Parra, Luis Alonso Herrera, Carlos Pérez-Plasencia

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 9 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 3 institutions in 1 country.

Eduardo López-UrrutiaGenomics Laboratory, UBIMED, Faculty of Higher Studies-Iztacala, National Autonomous University, Tlalnepantla, 54090 State of Mexico, Mexico.
Alma Campos-ParraGenomics Laboratory, National Cancer Institute of Mexico, Tlalpan, 14680 Mexico City, Mexico.
Luis Alonso HerreraEpigenetics Laboratory, National Cancer Institute of Mexico, Tlalpan, 14680 Mexico City, Mexico.
Carlos Pérez-PlasenciaGenomics Laboratory, UBIMED, Faculty of Higher Studies-Iztacala, National Autonomous University, Tlalnepantla, 54090 State of Mexico, Mexico.
Autonomous University of Tlaxcala · MXInstituto Nacional de Cancerología · MXNational Institute of Genomic Medicine · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is generally accepted that alternative splicing has an effect on disease when it leads to conspicuous changes in relevant proteins, but that the combinatorial effect of several small modifications can have marked outcomes as well. Inflammation is a complex process involving numerous signaling pathways, among which the tumor necrosis factor (TNF) pathway is one of the most studied. Signaling pathways are commonly represented as intricate cascades of molecular interactions that eventually lead to the activation of one or several genes. Alternative splicing is a common means of controlling protein expression in time and space; therefore, it can modulate the outcome of signaling pathways through small changes in their elements. Notably, the overall process is tightly regulated, which is easily overlooked when analyzing the pathway as a whole. The present review summarizes recent studies of the alternative splicing of key players of the TNF pathway leading to inflammation, and hypothesizes on the cumulative results of those modifications and the impact on cancer development.

Indexed as

alternative splicinginflammationTNF isoformsTNF signaling pathway

Identifiers

PMID29113151
PMCPMC5656035
OpenAlexW2752282596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.