Evidence map›Paper›PMID 26002011›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2015

Expression of metastasis-associated protein 3 in human brain glioma related to tumor prognosis.

Shouqin Shan, Guangyan Hui, Fanggao Hou, Hua Shi, Guoqing Zhou, Han Yan, Lu Wang, Jinfeng Liu

Abstract read
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In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  12. Advances in clinical neurology through the journal "Neurological Sciences" (2015-2016).Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
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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.

Shouqin ShanQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China. shanshouqin@yeah.net.
Guangyan HuiQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Fanggao HouQingdao Second Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Hua ShiQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Guoqing ZhouQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Han YanQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Lu WangQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Jinfeng LiuQingdao First Sanatorium of Jinan Military Region, Qingdao, 266071, Shandong, People's Republic of China.
Qingdao Eighth People's Hospital · CNPeople's Liberation Army 401 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma represents a disparate group of tumors characterized by high invasion ability, and therefore it is of clinical significance to identify molecular markers and therapeutic targets for better clinical management. Previously, metastasis-associated protein family (MTA) is considered to promote tumor cell invasion and metastasis of human malignancies. Recently, the newly identified MTA3 has been shown to play conflicting roles in human malignancies, while the expression pattern and potential clinical significance of MTA3 in human glioma have not been addressed yet. In the present study, we investigated the protein expression of MTA3 by immunohistochemistry assay and analyzed its association with glioma prognosis in 186 cases of patients. Results showed that MTA3 expression was decreased in glioma compared with that in normal brain (P < 0.05). In addition, tumors with high MTA3 expression were more likely to be of low WHO grade (P = 0.005) and reserve of body function (P = 0.014). Survival analysis showed that decreased MTA3 expression was independently associated with unfavorable overall survival of patients (P < 0.001). These results provide the first evidence that MTA3 expression was decreased in human glioma and negatively associated with prognosis of patients, suggesting that MTA3 may play a tumor suppressor role in glioma.

Indexed as

BiomarkersBrainBrain NeoplasmsDNA MethylationDNA Modification MethylasesDNA Repair EnzymesFemaleGene ExpressionGliomaHumansImmunohistochemistryKaplan-Meier EstimateMaleMiddle AgedNeoplasm ProteinsPrognosisBiomarkersDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanMTA3 protein, humanNeoplasm ProteinsTumor Suppressor ProteinsGliomaImmunohistochemistryMTA3Prognosis

Identifiers

PMID26002011
OpenAlexW236598522

What OpenQuestion holds

Textmetadata
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.