Evidence map›Paper›PMID 22920603›Full record

ArticleCancer cell international2012

Stromal proteome expression profile and muscle-invasive bladder cancer research.

Haitao Niu, Haiping Jiang, Bo Cheng, Xinhui Li, Qian Dong, Leping Shao, Shiguo Liu, Xinsheng Wang

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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.

Haitao Niu *Department of Urology, The Affiliated Hospital of Medical College Qingdao University, Qingdao, China.
Haiping Jiang *Department of Oncology, The Affiliated Hospital of Medical College Qingdao University, Qingdao, China.
Bo ChengDepartment of Urology, The Central Hospital of Shengli Oil Field, Dondying, China.
Xinhui LiDepartment of Urology, The Affiliated Hospital of Medical College Qingdao University, Qingdao, China.
Qian DongDepartment of Pediatric Surgery, The Affiliated Hospital of Medical College Qingdao University, Qingdao, China.
Leping ShaoDepartment of Nephrology, The Affiliated Hospital of Medical College Qingdao University, Qingdao, China.
Shiguo LiuGout Laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, China.
Xinsheng WangDepartment of Urology, The Affiliated Hospital of Medical College Qingdao University, Qingdao, China.
Qingdao University · CNShengli Oilfield Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo globally characterize the cancer stroma expression profile of muscle-invasive transitional cell carcinoma and to discuss the cancer biology as well as biomarker discovery from stroma. Laser capture micro dissection was used to harvest purified muscle-invasive bladder cancer stromal cells and normal urothelial stromal cells from 4 paired samples. Two-dimensional liquid chromatography tandem mass spectrometry was used to identify the proteome expression profile. The differential proteins were further analyzed using bioinformatics tools and compared with the published literature.

resultsWe identified 868/872 commonly expressed proteins and 978 differential proteins from 4 paired cancer and normal stromal samples using laser capture micro dissection coupled with two-dimensional liquid chromatography tandem mass spectrometry. 487/491 proteins uniquely expressed in cancer/normal stroma. Differential proteins were compared with the entire list of the international protein index (IPI), and there were 42/42 gene ontology (GO) terms exhibited as enriched and 8/5 exhibited as depleted in cellular Component, respectively. Significantly altered pathways between cancer/normal stroma mainly include metabolic pathways, ribosome, focal adhesion, etc. Finally, descriptive statistics show that the stromal proteins with extremes of PI and MW have the same probability to be a biomarker.

conclusionsBased on our results, stromal cells are essential component of the cancer, biomarker discovery and network based multi target therapy should consider neoplastic cells itself and corresponding stroma as whole one.

Identifiers

PMID22920603
PMCPMC3489783
OpenAlexW2154874745

What OpenQuestion holds

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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.