Evidence map›Paper›PMID 30764831›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

Landscape of tumor suppressor long noncoding RNAs in breast cancer.

Boran Pang, Qin Wang, Shipeng Ning, Junqiang Wu, Xingda Zhang, Yanbo Chen, Shouping Xu

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 56 citations in OpenAlex.

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  9. ROR1-AS1: A Meaningful Long Noncoding RNA in Oncogenesis.Mini reviews in medicinal chemistry · 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 3 institutions in 1 country.

Boran PangDepartment of Surgery, Rui Jin Hospital, Shanghai Key Laboratory of Gastric Neoplasm, Shanghai Institute of Digestive Surgery, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
Qin WangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Shipeng NingDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Junqiang WuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Xingda ZhangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Yanbo ChenDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Shouping XuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China. Shoupingxu@hrbmu.edu.cn.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CNShanghai Jiao Tong University · CN

Funding

Distinguished Young Scholars of Harbin Medical University Cancer Hospital JCQN2018-03National Natural Science Foundation of China 81602323National Natural Science Foundation of China 81872149Natural Science Foundation of Heilongjiang Province H201406Wu Lien-teh Science Foundation of Harbin Medical University WLD-QN1706Yong Elite Training Foundation Grant of Harbin Medical University Cancer Hospital JY2016-02
6 · The paper itself

Abstract

backgroundThe landscape and biological functions of tumor suppressor long noncoding RNAs in breast cancer are still unknown.

methodsData from whole transcriptome sequencing of 33 breast specimens in the Harbin Medical University Cancer Center cohort and The Cancer Genome Atlas was applied to identify and validate the landscape of tumor suppressor long noncoding RNAs, which was further validated by The Cancer Genome Atlas pancancer data including 33 cancer types and 12,839 patients. Next, the expression model, prognostic roles, potential biological functions and epigenetic regulation of tumor suppressor long noncoding RNAs were investigated and validated in the breast cancer and pancancer cohorts. Finally, EPB41L4A-AS2 was selected to validate our novel finding, and the tumor suppressive roles of EPB41L4A-AS2 in breast cancer were examined.

resultsWe identified and validated the landscape of tumor suppressor long noncoding RNAs in breast cancer. The expression of the identified long noncoding RNAs was downregulated in cancer tissue samples compared with normal tissue samples, and these long noncoding RNAs correlated with a favorable prognosis in breast cancer patients and the patients in the pancancer cohort. Multiple carcinogenesis-associated biological functions were predicted to be regulated negatively by these long noncoding RNAs. Moreover, these long noncoding RNAs were transcriptionally regulated by epigenetic modification, including DNA methylation and histone methylation modification. Finally, EPB41L4A-AS2 inhibited breast cancer cell proliferation, migration and invasion and induced cell apoptosis in vitro. Mechanistically, EPB41L4A-AS2, acting at least in part as a tumor suppressor, upregulated tumor suppressor gene expression. Moreover, ZNF217 recruited EZH2 to the EPB41L4A-AS2 locus and suppressed the expression of EPB41L4A-AS2 by epigenetically increasing H3K27me3 enrichment.

conclusionsThis work enlarges the functional landscape of known long noncoding RNAs in human cancer and provides novel insights into the suppressive roles of these long noncoding RNAs.

Indexed as

Genes, Tumor SuppressorBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansRNA, Long NoncodingTranscriptomeRNA, Long NoncodingBreast cancerEPB41L4A-AS2lncRNAsPrognosisTumorigenesis

Identifiers

PMID30764831
PMCPMC6376750
OpenAlexW2916763191

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LicenceCC BY
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Registered trials

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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.