Evidence map›Paper›PMID 28594403›Full record

ArticleCell death & disease2017

Long noncoding RNA CRNDE stabilized by hnRNPUL2 accelerates cell proliferation and migration in colorectal carcinoma via activating Ras/MAPK signaling pathways.

Huijuan Jiang, Yiqing Wang, Meiling Ai, Haowei Wang, Zhijiao Duan, Huanan Wang, Li Zhao, Jiang Yu, Yanqing Ding, Shuang Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
6.9field-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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it, 126 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  6. Review
  7. A Multi-Faceted Analysis ShowingInternational journal of molecular sciences · 2024
    Article
  8. CRNDE: A Pivotal Oncogenic Long Non-Coding RNA in Cancers.The Yale journal of biology and medicine · 2023
    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

10 authors at 2 institutions in 1 country.

Huijuan JiangDepartment of Pathology, Southern Medical University, Nanfang Hospital, Guangzhou, China.
Yiqing WangDepartment of Pathology, Southern Medical University, Nanfang Hospital, Guangzhou, China.
Meiling AiDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Haowei WangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Zhijiao DuanDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Huanan WangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Li ZhaoDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Jiang YuDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yanqing DingDepartment of Pathology, Southern Medical University, Nanfang Hospital, Guangzhou, China.
Shuang WangDepartment of Pathology, Southern Medical University, Nanfang Hospital, Guangzhou, China.
Southern Medical University · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have furthered our understanding of the function of long noncoding RNAs (lncRNAs) in numerous biological processes, including cancer. This study investigated the expression of a novel lncRNA, colorectal neoplasia differentially expressed (CRNDE), in colorectal carcinoma (CRC) tissues and cells by real-time RT-PCR and in situ hybridization, and its biological function using a series of in vitro and in vivo experiments to determine its potential as a prognostic marker and therapeutic target. CRNDE was found to be upregulated in primary CRC tissues and cells (P<0.05), and the upregulation of CRNDE expression is a powerful predictor of advanced TNM stage (P<0.05) and poor prognosis for CRC patients (P=0.002). The promoting effects of CRNDE on the cell proliferation, cell cycling and metastasis of CRC cells were confirmed both in vitro and in vivo by gain-of-function and loss-of-function experiments. Mechanistically, it was demonstrated that CRNDE could form a functional complex with heterogeneous nuclear ribonucleoprotein U-like 2 protein (hnRNPUL2) and direct the transport of hnRNPUL2 between the nucleus and cytoplasm. hnRNPUL2 that was accumulated in the cytoplasm could interact with CRNDE both physically and functionally, increasing the stability of CRNDE RNA. Moreover, gene expression profile data showed that CRNDE depletion in cells downregulated a series of genes involved in the Ras/mitogen-activated protein kinase signaling pathways. Collectively, these findings provide novel insights into the function and mechanism of lncRNA CRNDE in the pathogenesis of CRC and highlight its potential as a therapeutic target for CRC intervention.

Indexed as

Cell MovementCell ProliferationMAP Kinase Signaling SystemAnimalsCell Line, TumorColorectal NeoplasmsExtracellular Signal-Regulated MAP KinasesFemaleHeterogeneous-Nuclear RibonucleoproteinsHumansMaleMiceMice, Inbred BALB CMice, NudeProto-Oncogene Proteins p21(ras)RNA, Long NoncodingCRNDE RNA, humanExtracellular Signal-Regulated MAP KinasesHeterogeneous-Nuclear RibonucleoproteinshnRNPUL2 protein, humanProto-Oncogene Proteins p21(ras)RNA, Long NoncodingRNA, Neoplasm

Identifiers

PMID28594403
PMCPMC5520914
OpenAlexW2622909890

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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.