Evidence map›Paper›PMID 25755764›Full record

ArticleInternational journal of clinical and experimental pathology2015

TGFBI protein high expression predicts poor prognosis in colorectal cancer patients.

Jing Zhu, Xijun Chen, Zhongcai Liao, Chao He, Xiaotong Hu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.6field-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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 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

5 authors at 3 institutions in 1 country.

Jing ZhuBiomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province Hangzhou 30016, Zhejiang, China.
Xijun ChenBiomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province Hangzhou 30016, Zhejiang, China.
Zhongcai LiaoZhejiang Orient Gene Biotech Co., LTD Anji 313300, Zhejiang, China.
Chao HeBiomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province Hangzhou 30016, Zhejiang, China ; Department of Colorectal Surgery, Sir Run Run Shaw Hospital, Zhejiang University Hangzhou 30016, Zhejiang, China.
Xiaotong HuBiomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province Hangzhou 30016, Zhejiang, China.
Zhejiang Lab · CNHangzhou DAC Biotech (China) · CNSir Run Run Shaw Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transforming growth factor-beta-induced (TGFBI) serves as a linker protein and plays a role in the activation of morphogenesis, cell proliferation, adhesion, migration, differentiation and inflammation. High expression levels of the human TGFBI gene are correlated with numerous human malignancies. In order to explore the roles of TGFBI in the tumor progression of colorectal cancer, colorectal cancer specimens from 115 patients with strict follow-up were selected for the analysis of TGFBI by immunohistochemistry. The correlations between TGFBI expression and the clinicopathological features of colorectal cancers were evaluated. In the colorectal cancer tissues, TGFBI was mainly localized in the cytoplasm and stroma and scarcely in the nucleus. TGFBI expression in the cytoplasm and stroma was not found to be associated with age, gender, tumor histopathological grading, PT category and tumor location (P > 0.05 for each). However, high TGFBI expression in the cytoplasm and stroma correlated with lymph node metastasis, distant metastasis and Dukes stage (P < 0.05 for each). The survival rate was significantly lower in patients with high TGFBI expression than in those with low TGFBI expression. Furthermore, we found that tumor node metastasis (TNM) staging (HR: 2.963; 95% CI: 1.573-1.664; P = 0.000), differentiation (HR: 1.574; 95% CI: 1.001-2.476; P = 0.049) and high TGFBI cytoplasmic expression (HR: 3.332; 95% CI: 1.410-7.873; P = 0.000) proved to be independent prognostic factors for survival in colorectal cancer. In conclusion, TGFBI plays an important role in the progression of colorectal cancers and it is an independent poor prognostic factor for colorectal cancer patients.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overbetaIG-H3 ProteinBiomarkers, TumorColorectal NeoplasmsDisease ProgressionExtracellular Matrix ProteinsFemaleHumansImmunohistochemistryKaplan-Meier EstimateMaleMiddle AgedPrognosisbetaIG-H3 ProteinBiomarkers, TumorExtracellular Matrix ProteinsTransforming Growth Factor betacolorectal cancerimmunohistochemistryprognosisTGFBI

Identifiers

PMID25755764
PMCPMC4348825
OpenAlexW2406317775

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.