Evidence map›Paper›PMID 27829996›Full record

ArticleAmerican journal of translational research2016

Down-regulation of long non-coding RNA FOXD3 antisense RNA 1 (FOXD3-AS1) inhibits cell proliferation, migration, and invasion in malignant glioma cells.

Zhen-Hua Chen, Hong-Kang Hu, Chen-Ran Zhang, Cheng-Yin Lu, Yi Bao, Zheng Cai, Yong-Xiang Zou, Guo-Han Hu, Lei Jiang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
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  14. LncRNACancer management and research · 2021
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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.

Zhen-Hua ChenDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical UniversityShanghai, China; Department of Neurosurgery, The First People's Hospital of Nantong, Medical School of Nantong UniversityJiangsu Province, China.
Hong-Kang HuDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical University Shanghai, China.
Chen-Ran ZhangDepartment of Pediatric Neurosurgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Cheng-Yin LuDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical University Shanghai, China.
Yi BaoDepartment of Endocrinology, Changzheng Hospital, Second Military Medical University Shanghai, China.
Zheng CaiDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical University Shanghai, China.
Yong-Xiang ZouDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical University Shanghai, China.
Guo-Han HuDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical University Shanghai, China.
Lei JiangDepartment of Neurosurgery, Changzheng Hospital, Second Military Medical University Shanghai, China.
Second Military Medical University · CNXinHua Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence indicates that long non-coding RNAs (lncRNAs) play key roles in cancer initiation and progression. However, little is known about the therapeutic significance of lncRNAs in glioma. In this study, we explored the tumorigenic role of a classical lncRNA, FOXD3 antisense RNA 1 (FOXD3-AS1) in glioma. Systemic analysis of the patient specimens and clinical data showed that FOXD3-AS1 was markedly up-regulated in high-grade glioma tissues (WHO grade III-IV) compared with that in low-grade glioma (WHO grade I-II) and normal brain tissues (both P<0.01), and patients with low FOXD3-AS1 expression had grater survival probability. Multivariate regression analysis showed that increased FOXD3-AS1 expression was a significant independent indicator of poor prognosis in glioma patients (P=0.034). To understand the tumorigenic mechanism of FOXD3-AS1, the expression pattern and functional role of FOXD3-AS1 in glioma were detected using real-time PCR and Smart Silencer-mediated knockdown study. In related cell biological assays, we discovered that FOXD3-AS1 knockdown significantly inhibited cell proliferation, induced cell cycle S-phase arrest, and impaired cell migration and invasion in malignant glioma cells. As expected, we also found that the expression of FOXD3-AS1 was positively correlated with FOXD3 mRNA. Knockdown of FOXD3-AS1 reduced the protein level of FOXD3 in cultured U251 and A172 cell lines. These results suggest that FOXD3-AS1 is an oncogenic lncRNA, which may promote the occurrence and development of glioma through transcriptional regulation of FOXD3.

Indexed as

FOXD3FOXD3-AS1gliomaLong non-coding RNA

Identifiers

PMID27829996
PMCPMC5095305
OpenAlexW2576366150

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.