Evidence map›Paper›PMID 28600503›Full record

ArticleScientific reports2017

Transcriptome sequencing identifies ANLN as a promising prognostic biomarker in bladder urothelial carcinoma.

Shuxiong Zeng, Xiaowen Yu, Chong Ma, Ruixiang Song, Zhensheng Zhang, Xiaoyuan Zi, Xin Chen, Yang Wang, Yongwei Yu, Junjie Zhao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.4field-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

51 citing papers in PubMed, 74 citations in OpenAlex.

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  18. NInternational journal of biological sciences · 2023
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  19. ScreeningFrontiers in genetics · 2023
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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.

Shuxiong ZengDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Xiaowen YuDepartment of Geriatrics, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Chong MaDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Ruixiang SongDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Zhensheng ZhangDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Xiaoyuan ZiDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Xin ChenDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Yang WangDepartment of Pathology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Yongwei YuDepartment of Pathology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Junjie ZhaoDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Rongchao WeiDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China.
Yinghao SunDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China. sunyh@medmail.com.cn.
Chuanliang XuDepartment of Urology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China. xuchuanliang@vip.126.com.
Changhai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of bladder urothelial carcinoma (BLCA) varies greatly even for patients with similar pathological characteristics. We conducted transcriptome sequencing on ten pairs of BLCA samples and adjacent normal tissues to identify differentially expressed genes. Anillin (ANLN) was identified as a transcript that was significantly up-regulated in BLCA samples compared with normal tissues. Prognostic power of candidate gene was studied using qRT-PCR and immunohistochemistry on 40 and 209 patients, respectively. Patients with elevated ANLN expression level was correlated with poorer cancer-specific (median, 22.4 vs. 37.3 months, p = 0.001), progression-free (median, 19.7 vs. 27.9 months, p = 0.001) and recurrence-free survival (median, 17.1 vs. 25.2 months, p = 0.011) compared with low ANLN expression. Public datasets TCGA and NCBI-GEO were analyzed for external validation. Knockdown of ANLN in J82 and 5637 cells using small interfering RNA significantly inhibited cell proliferation, migration, and invasion ability. Moreover, knockdown of ANLN resulted in G2/M phase arrest and decreased expression of cyclin B1 and D1. Microarray analysis suggested that ANLN played a major role in cell migration and was closely associated with several cancer-related signaling pathways. In conclusion, ANLN was identified as a promising prognostic biomarker which could be used to stratify different risks of BLCA.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptomeAnimalsBiomarkers, TumorCarcinoma in SituCell Line, TumorCell MovementCell ProliferationCyclin B1Cyclin D1Datasets as TopicG2 Phase Cell Cycle CheckpointsHigh-Throughput Nucleotide SequencingHumansMiceMicroarray AnalysisANLN protein, humanBiomarkers, TumorCCNB1 protein, humanCCND1 protein, humanCyclin B1Cyclin D1Microfilament ProteinsRNA, Small Interfering

Identifiers

PMID28600503
PMCPMC5466664
OpenAlexW2623210147

What OpenQuestion holds

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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.