Evidence map›Paper›PMID 25846736›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

Clinical significance and biological roles of TRIM24 in human bladder carcinoma.

Dongwei Xue, Xiuwei Zhang, Xilin Zhang, Jia Liu, Ning Li, Chunlai Liu, Yili Liu, Ping Wang

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

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  17. Regulation of TRIM24 by miR-511 modulates cell proliferation in gastric cancer.Journal of experimental & clinical cancer research : CR · 2017
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  19. Histone H3 lysine 23 acetylation is associated with oncogene TRIM24 expression and a poor prognosis in breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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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

8 authors at 2 institutions in 1 country.

Dongwei XueDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Xiuwei ZhangDepartment of Pathology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Xilin ZhangDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Jia LiuDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Ning LiDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Chunlai LiuDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Yili LiuDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Ping WangDepartment of Urology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China. wangpingcmu@126.com.
China Medical University · CNFourth Affiliated Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tripartite motif-containing 24 (TRIM24), also known as transcription intermediary factor 1-alpha (TIF1α), is a chromatin-associated protein which as been has been implicated in carcinogenesis. However, its expression profile and biological roles in human bladder carcinoma has not been investigated. In this study, we examined its expression in 95 bladder cancer specimens. We found that TRIM24 expression was upregulated in 39 of 95 (41.1 %) specimens compared with normal control. TRIM24 overexpression was associated with local invasion and advanced grade of bladder cancer. In addition, we transfected TRIM24 plasmid into BIU-87 cell line and TRIM24 siRNA into 5637 cell line. Colony formation, CCK-8, and transwell assay were used to assess its biological roles in bladder cancer cells. The result showed that TRIM24 could facilitate cancer cell growth and invading ability. Western blot analysis demonstrated that TRIM24 upregulated cyclin D1, cyclin E, p-IκBα, and p-AKT expression, suggesting TRIM24 activates NF-κB and AKT pathways. In addition, NF-κB inhibitor reversed the effect of TRIM24 on cyclin D1. In conclusion, TRIM24 is overexpressed in human bladder cancer and facilitates bladder cancer growth and invasion, possibly through NF-κB and AKT signaling pathways.

Indexed as

AgedApoptosisCarcinomaCarrier ProteinsCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm ProteinsNeoplasm StagingNF-kappa BOncogene Protein v-aktSignal TransductionUrinary Bladder NeoplasmsCarrier ProteinsNeoplasm ProteinsNF-kappa BOncogene Protein v-aktTRIM24 protein, humanAKTBladder cancerNF-κBProliferationTRIM24

Identifiers

PMID25846736
OpenAlexW2043259832

What OpenQuestion holds

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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.