Evidence map›Paper›PMID 30122991›Full record

ArticleCancer management and research2018

TMEM17 promotes malignant progression of breast cancer via AKT/GSK3β signaling.

Yue Zhao, Kuiyuan Song, Yong Zhang, Hongtao Xu, Xiupeng Zhang, Liang Wang, Chuifeng Fan, Guiyang Jiang, Enhua Wang

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 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

9 authors at 2 institutions in 1 country.

Yue ZhaoDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Kuiyuan SongDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Yong ZhangDepartments of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, China.
Hongtao XuDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Xiupeng ZhangDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Liang WangDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Chuifeng FanDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Guiyang JiangDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
Enhua WangDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China, jianggy@hotmail.com.
First Hospital of China Medical University · CNLiaoning Cancer Hospital & Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCurrent knowledge of TMEM17, a recently identified protein of the transmembrane (TMEM) family, is limited, especially with respect to its expression and biological functions in malignant tumors. This study analyzed TMEM17 expression in invasive breast cancer tissue and breast cell lines and its relevance to clinicopathological factors, and investigated the mechanisms underlying the biological effects of TMEM17 on breast cancer cells. PATIENTS AND

methodsTMEM17 protein expression was determined in 20 freshly harvested specimens (tumor and paired normal tissues) by Western blotting. Immunohistochemical analysis was performed to determine the expression and subcellular localization of TMEM17 in samples from 167 patients (mean age, 49 years) diagnosed with invasive ductal carcinoma (38 with triple-negative breast cancer; 129 with non-triple-negative breast cancer) who underwent complete resection in the First Affiliated Hospital of China Medical University between 2011 and 2013. Furthermore, TMEM17 was knocked down by small interfering RNAs in breast cancer cell lines.

resultsTMEM17 was found to be significantly upregulated in breast cancer tissues compared to the corresponding normal breast tissues by Western blotting (

conclusionOur results indicate that TMEM17 is upregulated in breast cancer tissues and can promote malignant progression of breast cancer cells by activating the AKT/GSK3β signaling pathway.

Indexed as

invasionmigrationproliferationSnailβ-catenin

Identifiers

PMID30122991
PMCPMC6080873
OpenAlexW2885569596

What OpenQuestion holds

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LicenceCC BY-NC
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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.