Evidence map›Paper›PMID 28496199›Full record

ArticleExperimental & molecular medicine2017

Upregulation and biological function of transmembrane protein 119 in osteosarcoma.

Zhen-Huan Jiang, Jun Peng, Hui-Lin Yang, Xing-Li Fu, Jin-Zhi Wang, Lei Liu, Jian-Nong Jiang, Yong-Fei Tan, Zhi-Jun Ge

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-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

25 citing papers in PubMed, 43 citations in OpenAlex.

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  6. International journal of molecular sciences · 2024
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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 4 institutions in 1 country.

Zhen-Huan JiangDepartment of Orthopedics, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People's Republic of China.
Jun PengDepartment of Orthopedics, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People's Republic of China.
Hui-Lin YangDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, People's Republic of China.
Xing-Li FuHealth Science Center of Jiangsu University, Zhenjiang, People's Republic of China.
Jin-Zhi WangDepartment of Cell Biology, School of Medicine, Soochow University, Suzhou, People's Republic of China.
Lei LiuDepartment of Orthopedics, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People's Republic of China.
Jian-Nong JiangDepartment of Orthopedics, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People's Republic of China.
Yong-Fei TanDepartment of Critical Care Medicine, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People's Republic of China.
Zhi-Jun GeDepartment of Critical Care Medicine, The Affiliated Yixing Hospital of Jiangsu University, Yixing, People's Republic of China.
Jiangsu University · CNYixing People's Hospital · CNFirst Affiliated Hospital of Soochow University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is suggested to be caused by genetic and molecular alterations that disrupt osteoblast differentiation. Recent studies have reported that transmembrane protein 119 (TMEM119) contributes to osteoblast differentiation and bone development. However, the level of TMEM119 expression and its roles in osteosarcoma have not yet been elucidated. In the present study, TMEM119 mRNA and protein expression was found to be up-regulated in osteosarcoma compared with normal bone cyst tissues. The level of TMEM119 protein expression was strongly associated with tumor size, clinical stage, distant metastasis and overall survival time. Moreover, gene set enrichment analysis (GSEA) of the Gene Expression Omnibus (GEO) GSE42352 dataset revealed TMEM119 expression in osteosarcoma tissues to be positively correlated with cell cycle, apoptosis, metastasis and TGF-β signaling. We then knocked down TMEM119 expression in U2OS and MG63 cells using small interfering RNA, which revealed that downregulation of TMEM119 could inhibit the proliferation of osteosarcoma cells by inducing cell cycle arrest in G0/G1 phase and apoptosis. We also found that TMEM119 knockdown significantly inhibited cell migration and invasion, and decreased the expression of TGF-β pathway-related factors (BMP2, BMP7 and TGF-β). TGF-β application rescued the inhibitory effects of TMEM119 knockdown on osteosarcoma cell migration and invasion. Further in vitro experiments with a TGF-β inhibitor (SB431542) or BMP inhibitor (dorsomorphin) suggested that TMEM119 significantly promotes cell migration and invasion, partly through TGF-β/BMP signaling. In conclusion, our data support the notion that TMEM119 contributes to the proliferation, migration and invasion of osteosarcoma cells, and functions as an oncogene in osteosarcoma.

Indexed as

Up-RegulationAdolescentAnimalsApoptosisBone Morphogenetic Protein 2Bone Morphogenetic Protein 7Bone NeoplasmsCell CycleCell Line, TumorCell MovementCell ProliferationCells, CulturedFemaleHEK293 CellsHumansMaleBMP2 protein, humanBMP7 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 7Membrane ProteinsTmem119 protein, humanTransforming Growth Factor beta

Identifiers

PMID28496199
PMCPMC5454443
OpenAlexW2614019591

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.