Evidence map›Paper›PMID 28088793›Full record

ArticleOncotarget2017

HnRNP-L mediates bladder cancer progression by inhibiting apoptotic signaling and enhancing MAPK signaling pathways.

Daojun Lv, Huayan Wu, Rongwei Xing, Fangpeng Shu, Bin Lei, Chengyong Lei, Xumin Zhou, Bo Wan, Yu Yang, Liren Zhong and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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  19. lncITPF Promotes Pulmonary Fibrosis by Targeting hnRNP-L Depending on Its Host Gene ITGBL1.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
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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

12 authors at 3 institutions in 1 country.

Daojun LvDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Huayan WuDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Rongwei XingDepartment of Urology, Affiliated Weihai Second Municipal Hospital of Qingdao University, Weihai 264200, P. R. China.
Fangpeng ShuDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Bin LeiDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Chengyong LeiDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Xumin ZhouDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Bo WanDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Yu YangDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen PKU-HKUST Medical Center, Shenzhen, Guangdong Province, 518036, China.
Liren ZhongDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Xiangming MaoDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Yaguang ZouDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
Nanfang Hospital · CNSouthern Medical University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterogeneous nuclear ribonucleoprotein L (hnRNP-L) is a promoter of various kinds of cancers, but its actions in bladder cancer (BC) are unclear. In this study, we investigated the function and the underlying mechanism of hnRNP-L in bladder carcinogenesis. Our results demonstrated that enhanced hnRNP-L expression in BC tissues was associated with poor overall survival of BC patients. Depletion of hnRNP-L significantly suppressed cell proliferation in vitro and inhibited xenograft tumor growth in vivo. Furthermore, downregulation of hnRNP-L resulted in G1-phase cell cycle arrest and enhanced apoptosis accompanied by inhibition of EMT and cell migration. All these cellular changes were reversed by ectopic expression of hnRNP-L. Deletion of hnRNP-L resulted in decreased expression of Bcl-2, enhanced expression of caspases-3, -6 and -9 and inhibition of the MAPK signaling pathway. These findings demonstrate that hnRNP-L contributes to poor prognosis and tumor progression of BC by inhibiting the intrinsic apoptotic signaling and enhancing MAPK signaling pathways.

Indexed as

MAP Kinase Signaling SystemApoptosisCell Cycle CheckpointsCell MovementCell ProliferationDisease ProgressionFemaleHeterogeneous-Nuclear Ribonucleoprotein LHumansMaleMiddle AgedSignal TransductionUp-RegulationUrinary Bladder NeoplasmsHeterogeneous-Nuclear Ribonucleoprotein Lbladder cancerepithelial-mesenchymal transitionheterogeneous nuclear ribonucleoprotein Lintrinsic apoptosisMAPK

Identifiers

PMID28088793
PMCPMC5355122
OpenAlexW2575357329

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.