Evidence map›Paper›PMID 30216655›Full record

ArticleMolecular oncology2018

A pan-cancer atlas of cancer hallmark-associated candidate driver lncRNAs.

Yulan Deng, Shangyi Luo, Xinxin Zhang, Chaoxia Zou, Huating Yuan, Gaoming Liao, Liwen Xu, Chunyu Deng, Yujia Lan, Tingting Zhao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Long Non-Coding RNAs as "MYC Facilitators".Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
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  10. International journal of molecular sciences · 2020
    Article
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  14. Observational
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  16. Review
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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

13 authors at 2 institutions in 1 country.

Yulan DengCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Shangyi LuoCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Xinxin ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Chaoxia ZouDepartment of Biochemistry and Molecular Biology, Harbin Medical University, China.
Huating YuanCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Gaoming LiaoCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Liwen XuCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Chunyu DengCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Yujia LanCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Tingting ZhaoDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, China.
Xu GaoDepartment of Biochemistry and Molecular Biology, Harbin Medical University, China.
Yun XiaoCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Xia LiCollege of Bioinformatics Science and Technology, Harbin Medical University, China.
Harbin Medical University · CNMinistry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Substantial cancer genome sequencing efforts have discovered many important driver genes contributing to tumorigenesis. However, very little is known about the genetic alterations of long non-coding RNAs (lncRNAs) in cancer. Thus, there is a need for systematic surveys of driver lncRNAs. Through integrative analysis of 5918 tumors across 11 cancer types, we revealed that lncRNAs have undergone dramatic genomic alterations, many of which are mutually exclusive with well-known cancer genes. Using the hypothesis of functional redundancy of mutual exclusivity, we developed a computational framework to identify driver lncRNAs associated with different cancer hallmarks. Applying it to pan-cancer data, we identified 378 candidate driver lncRNAs whose genomic features highly resemble the known cancer driver genes (e.g. high conservation and early replication). We further validated the candidate driver lncRNAs involved in 'Tissue Invasion and Metastasis' in lung adenocarcinoma and breast cancer, and also highlighted their potential roles in improving clinical outcomes. In summary, we have generated a comprehensive landscape of cancer candidate driver lncRNAs that could act as a starting point for future functional explorations, as well as the identification of biomarkers and lncRNA-based target therapy.

Indexed as

Databases, GeneticGene Expression Regulation, NeoplasticGene Regulatory NetworksNeoplasmsRNA, Long NoncodingRNA, NeoplasmHumansRNA, Long NoncodingRNA, Neoplasmcancer hallmarkcopy number alterationdriver lncRNAmutual exclusivitypan-cancer atlas

Identifiers

PMID30216655
PMCPMC6210054
OpenAlexW2889862113

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.