Evidence map›Paper›PMID 25193023›Full record

ArticleJournal of neuro-oncology2015

Romo1 is associated with ROS production and cellular growth in human gliomas.

Mi Ok Yu, Na-Hyun Song, Kyung-Jae Park, Dong-Hyuk Park, Se-Hyuk Kim, Yang-Seok Chae, Yong-Gu Chung, Sung-Gil Chi, Shin-Hyuk Kang

Abstract read
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In one paragraph

Article in Journal of neuro-oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

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  18. ROMO1 links oxidative stress to mitochondrial integrity.Journal of cell communication and signaling · 2015
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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.

Mi Ok YuDepartment of Neurosurgery College of Medicine, Korea University, #126, 5-ga, Anam-Dong, Seongbuk-Gu, Seoul, 136-705, Korea.
Na-Hyun Song
Kyung-Jae Park
Dong-Hyuk Park
Se-Hyuk Kim
Yang-Seok Chae
Yong-Gu Chung
Sung-Gil Chi
Shin-Hyuk Kang
Korea University · KRAjou University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Romo1 is a mitochondrial protein whose elevated expression is commonly observed in various types of human cancers. However, the expression status of Romo1 and its implication in the pathogenesis of human glioblastoma (GBM) remain largely undefined. To understand the role of Romo1 in the progression of GBM, we explored its expression in a series of GBM tissues and cell lines and determined its effect on ROS production, cell proliferation, and tumor growth. Romo1 was frequently overexpressed at the mRNA level in both primary tumors and cell lines and its elevation was more commonly observed in high grade tumors versus low grade tumors. Romo1 expression was associated with ROS production and its knockdown led to a marked reduction of in vitro cellular growth and anchorage-independent growth of GBM. Consistently, Romo1 depletion induced a G2/M arrest of the cell cycle that was accompanied with accumulation of phospho-cdc2. Furthermore, a mouse xenograft assay revealed that Romo1 depletion significantly decreased tumor formation and growth. Therefore, our data demonstrate that Romo1 upregulation is a common event in human GBMs and contributes to the malignant tumor progression, suggesting that Romo1 could be a new therapeutic target for human GBM.

Indexed as

AnimalsBrainBrain NeoplasmsCarcinogenesisCell CycleCell Line, TumorCell ProliferationGene Knockdown TechniquesGliomaHumansMembrane ProteinsMiceMitochondrial ProteinsNeoplasm GradingNeoplasm TransplantationReactive Oxygen SpeciesMembrane ProteinsMitochondrial ProteinsReactive Oxygen SpeciesRNA, MessengerROMO1 protein, human

Identifiers

PMID25193023
OpenAlexW2077573942

What OpenQuestion holds

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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.