Evidence map›Paper›PMID 26862852›Full record

ArticleOncotarget2016

Non-coding RNA LINC00857 is predictive of poor patient survival and promotes tumor progression via cell cycle regulation in lung cancer.

Lihui Wang, Yanli He, Weijun Liu, Shengbin Bai, Lei Xiao, Jie Zhang, Saravana M Dhanasekaran, Zhuwen Wang, Shanker Kalyana-Sundaram, O Alejandro Balbin and 11 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  20. mFrontiers in oncology · 2021
    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

21 authors at 6 institutions in 2 countries.

Lihui WangGuangxi Medical University, Nanning, China.
Yanli HeSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Weijun LiuSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Shengbin BaiSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Lei XiaoSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Jie ZhangSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Saravana M DhanasekaranDepartment of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America.
Zhuwen WangSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Shanker Kalyana-SundaramDepartment of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America.
O Alejandro BalbinDepartment of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America.
Sudhanshu ShuklaDepartment of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America.
Yi LuGuangxi Medical University, Nanning, China.
Jules LinSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Rishindra M ReddySection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Philip W CarrottSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
William R LynchSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Andrew C ChangSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Arul M ChinnaiyanDepartment of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America.
David G BeerSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
Jian ZhangGuangxi Medical University, Nanning, China.
Guoan ChenSection of Thoracic Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, United States of America.
University of Michigan–Ann Arbor · USMichigan United · USFirst People's Hospital of Yunnan Province · CNGuangxi Medical University · CNXi'an Jiaotong University · CNXinjiang Medical University · CN

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Proteogenomics of Cancer Training ProgramT32CA140044 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAO, ARVIND, SARTOR, MAUREEN AGNES · 2010 to 2024
$3.9M
Identification and Characterization of Gene Fusions in Lung AdenocarcinomaR01CA154365 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BEER, DAVID GEORGE, CHINNAIYAN, ARUL M · 2011 to 2015
$1.4M
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA154365NCI NIH HHS T32 CA140044
6 · The paper itself

Abstract

We employed next generation RNA sequencing analysis to reveal dysregulated long non-coding RNAs (lncRNAs) in lung cancer utilizing 461 lung adenocarcinomas (LUAD) and 156 normal lung tissues from 3 separate institutions. We identified 281 lncRNAs with significant differential-expression between LUAD and normal lung tissue. LINC00857, a top deregulated lncRNAs, was overexpressed in tumors and significantly associated with poor survival in LUAD. knockdown of LINC00857 with siRNAs decreased tumor cell proliferation, colony formation, migration and invasion in vitro, as well as tumor growth in vivo. Overexpression of LINC00857 increased cancer cell proliferation, colony formation and invasion. Mechanistic analyses indicated that LINC00857 mediates tumor progression via cell cycle regulation. Our study highlights the diagnostic/prognostic potential of LINC00857 in LUAD besides delineating the functional and mechanistic aspects of its aberrant disease specific expression and potentially using as a new therapeutic target.

Indexed as

Biomarkers, TumorCell Cycle CheckpointsCell Line, TumorCell ProliferationDisease ProgressionHumansLung NeoplasmsPrognosisRNA, Long NoncodingRNA, NeoplasmSurvival AnalysisTransfectionBiomarkers, TumorLINC00857 lnc, humanRNA, Long NoncodingRNA, NeoplasmdiagnosisLINC00857lung adenocarcinomanon-coding RNAprognosis

Identifiers

PMID26862852
PMCPMC4905488
OpenAlexW2341867436

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.