Evidence map›Paper›PMID 23421905›Full record

ArticleOmics : a journal of integrative biology2013

Alternative polyadenylation in glioblastoma multiforme and changes in predicted RNA binding protein profiles.

Jiaofang Shao, Jing Zhang, Zengming Zhang, Huawei Jiang, Xiaoyan Lou, Bingding Huang, Gregory Foltz, Qing Lan, Qiang Huang, Biaoyang Lin

Open access · greenAbstract read
In one paragraph

Article in Omics : a journal of integrative biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. RNA-binding protein signaling in adult neurogenesis.Frontiers in cell and developmental biology · 2022
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Myocyte enhancer factor 2D promotes tumorigenicity in malignant glioma cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  12. Article
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

10 authors at 5 institutions in 4 countries.

Jiaofang ShaoSystems Biology Division, Zhejiang-California International NanoSystems Institute, Zhejiang University, Hangzhou, China.
Jing Zhang
Zengming Zhang
Huawei Jiang
Xiaoyan Lou
Bingding Huang
Gregory Foltz
Qing Lan
Qiang Huang
Biaoyang Lin
Zhejiang University · CNNeuroscience Institute · ITSecond Affiliated Hospital of Soochow University · CNSoochow University · CNSwedish Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative polyadenylation (APA) is widely present in the human genome and plays a key role in carcinogenesis. We conducted a comprehensive analysis of the APA products in glioblastoma multiforme (GBM, one of the most lethal brain tumors) and normal brain tissues and further developed a computational pipeline, RNAelements (http://sysbio.zju.edu.cn/RNAelements/), using covariance model from known RNA binding protein (RBP) targets acquired by RNA Immunoprecipitation (RIP) analysis. We identified 4530 APA isoforms for 2733 genes in GBM, and found that 182 APA isoforms from 148 genes showed significant differential expression between normal and GBM brain tissues. We then focused on three genes with long and short APA isoforms that show inconsistent expression changes between normal and GBM brain tissues. These were myocyte enhancer factor 2D, heat shock factor binding protein 1, and polyhomeotic homolog 1 (Drosophila). Using the RNAelements program, we found that RBP binding sites were enriched in the alternative regions between the first and the last polyadenylation sites, which would result in the short APA forms escaping regulation from those RNA binding proteins. To the best of our knowledge, this report is the first comprehensive APA isoform dataset for GBM and normal brain tissues. Additionally, we demonstrated a putative novel APA-mediated mechanism for controlling RNA stability and translation for APA isoforms. These observations collectively lay a foundation for novel diagnostics and molecular mechanisms that can inform future therapeutic interventions for GBM.

Indexed as

Base SequenceBinding SitesBrainBrain NeoplasmsCell Line, TumorDatabases, Nucleic AcidGlioblastomaHeat-Shock ProteinsHumansMADS Domain ProteinsMEF2 Transcription FactorsMyogenic Regulatory FactorsNeoplasm ProteinsPolyadenylationPolycomb Repressive Complex 1RNA-Binding ProteinsHeat-Shock ProteinsHSBP1 protein, humanMADS Domain ProteinsMEF2D protein, humanMEF2 Transcription FactorsMyogenic Regulatory FactorsNeoplasm ProteinsPHC1 protein, humanPolycomb Repressive Complex 1RNA-Binding ProteinsRNA, NeoplasmRNA Precursors

Identifiers

PMID23421905
PMCPMC3603499
OpenAlexW2092121586

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.