Evidence map›Paper›PMID 32075558›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2020

An atlas of transposable element-derived alternative splicing in cancer.

Evan A Clayton, Lavanya Rishishwar, Tzu-Chuan Huang, Saurabh Gulati, Dongjo Ban, John F McDonald, I King Jordan

Open access · greenAbstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
10.7field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

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  13. Alternative splicing of transposable elements in human breast cancer.bioRxiv : the preprint server for biology · 2024
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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

7 authors at 1 institution in 2 countries.

Evan A ClaytonIntegrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Lavanya RishishwarSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Tzu-Chuan HuangSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Saurabh GulatiSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Dongjo BanIntegrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
John F McDonaldIntegrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
I King JordanSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Georgia Institute of Technology · US

Funding

A Computational Biology and Predictive Health Genomics Training Program at GTT32GM105490 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GIBSON, GREGORY C · 2014 to 2018
$901k
NIGMS NIH HHS T32 GM105490
6 · The paper itself

Abstract

Transposable element (TE)-derived sequences comprise more than half of the human genome, and their presence has been documented to alter gene expression in a number of different ways, including the generation of alternatively spliced transcript isoforms. Alternative splicing has been associated with tumorigenesis for a number of different cancers. The objective of this study was to broadly characterize the role of human TEs in generating alternatively spliced transcript isoforms in cancer. To do so, we screened for the presence of TE-derived sequences co-located with alternative splice sites that are differentially used in normal versus cancer tissues. We analysed a comprehensive set of alternative splice variants characterized for 614 matched normal-tumour tissue pairs across 13 cancer types, resulting in the discovery of 4820 TE-generated alternative splice events distributed among 723 cancer-associated genes. Short interspersed nuclear elements (Alu) and long interspersed nuclear elements (L1) were found to contribute the majority of TE-generated alternative splice sites in cancer genes. A number of cancer-associated genes, including

Indexed as

Alternative SplicingGenome, HumanDNA Transposable ElementsHumansNeoplasmsDNA Transposable Elementsalternative splicingcancergene expressiongene regulationtransposable elementstumorigenesis

Identifiers

PMID32075558
PMCPMC7061986
OpenAlexW3005290476

What OpenQuestion holds

Textmetadata
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.