Evidence map›Paper›PMID 22215415›Full record

ArticleMedical oncology (Northwood, London, England)2012

Identification of novel serological tumor markers for human prostate cancer using integrative transcriptome and proteome analysis.

Zhao-dong Han, Yan-qiong Zhang, Hui-chan He, Qi-shan Dai, Guo-qiang Qin, Jia-hong Chen, Chao Cai, Xin Fu, Xue-cheng Bi, Jian-guo Zhu and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-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

28 citing papers in PubMed, 45 citations in OpenAlex.

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  17. Transcriptomic and Proteomic Investigation of HSP90A as a Potential Biomarker for HCC.Medical science monitor : international medical journal of experimental and clinical research · 2015
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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

15 authors at 7 institutions in 1 country.

Zhao-dong HanDepartment of Urology, Guangzhou First Municipal People's Hospital, Affiliated Guangzhou Medical College, Guangzhou, 510180, China.
Yan-qiong Zhang
Hui-chan He
Qi-shan Dai
Guo-qiang Qin
Jia-hong Chen
Chao Cai
Xin Fu
Xue-cheng Bi
Jian-guo Zhu
Dong-jiang Liao
Xin-peng Lu
Zi-yao Mo
Yun-ping Zhu
Wei-de Zhong
Guangzhou First People's Hospital · CNGuangzhou Medical University · CNState Key Laboratory of Respiratory Disease · CNBeijing Proteome Research Center · CNGuangdong Provincial People's Hospital · CNGuizhou Provincial People's Hospital · CNKey Laboratory of Guangdong Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to identify novel serological tumor markers for human prostate cancer (PCa). We compared the gene expression profile of PCa tissues to adjacent benign tissues of prostate using gene expression microarray. 1207 genes that were consistently different from adjacent benign tissues of prostate (paired t test, P<0.05) were selected as differentially expressed genes (DEGs). Among them, 652 DEGs were upregulated in PCa, whereas 555 DEGs were downregulated in PCa. In addition, two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with MS was performed to screen for candidate markers in the proteome of PCa and adjacent benign tissues of prostate. A total of 89 spots were significantly up-regulated (ratio≥2, P<0.01) in PCa samples, whereas 66 spots were down-regulated (ratio≤-2, P<0.01). Sixty gene products were identified among these spots. Moreover, 14 potential candidate markers, which were identified as differentially expressed molecules by both gene expression microarray and 2D-DIGE, were chosen for validation and analysis by ELISA. The serum levels of three proteins correlated well with the 2D-DIGE results. Furthermore, the increased serum level of Inosine monophosphate dehydrogenase II (IMPDH2) was significantly associated with the clinicopathological features of the patients with PCa, suggesting its potential as a serological tumor marker. These results demonstrated that integrative transcriptome and proteome analysis could be a powerful tool for marker discovery in PCa. We suggest IMPDH2 as a novel serological tumor marker for detection of early PCa and evaluation of tumor progression.

Indexed as

TranscriptomeAgedAged, 80 and overBiomarkers, TumorCarbon-Carbon LigasesEnzyme-Linked Immunosorbent AssayGene Expression ProfilingHSP90 Heat-Shock ProteinsHumansIMP DehydrogenaseMaleMiddle AgedNeoplasm ProteinsProstatic NeoplasmsProteomicsTwo-Dimensional Difference Gel ElectrophoresisBiomarkers, TumorCarbon-Carbon LigasesHSP90 Heat-Shock ProteinsIMP DehydrogenaseIMPDH2 protein, humanmethylcrotonoyl-CoA carboxylaseNeoplasm ProteinsTRAP1 protein, human

Identifiers

PMID22215415
OpenAlexW2094941740

What OpenQuestion holds

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Read underepoch 390

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.