Evidence map›Paper›PMID 33294261›Full record

ArticleAmerican journal of cancer research2020

Long non-coding RNA FOXD1-AS1 promotes the progression and glycolysis of nasopharyngeal carcinoma by sustaining FOXD1 expression.

Zhanwang Wang, Yaxin Cheng, Yuxing Zhu, Xueying Hu, Yi Jin, Lian Gong, Mengqing Xiao, Liang Xiang, Qinghai Zeng, Jianye Liu and 6 more

Open access · goldAbstract read
In one paragraph

Article in American journal of cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed, 10 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

16 authors at 1 institution in 1 country.

Zhanwang WangDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Yaxin ChengDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Yuxing ZhuDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Xueying HuDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Yi JinDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Lian GongDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Mengqing XiaoDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Liang XiangDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Qinghai ZengDepartment of Dermatology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Jianye LiuDepartment of Urology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Xingyu ChenDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Yeyu ZhangDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Xiaoming LiuDepartment of Gastroenterology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Liping DengDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Dong HeDepartment of Respiratory, The Second People's Hospital of Hunan Province Changsha 410007, China.
Ke CaoDepartment of Oncology, Third Xiangya Hospital of Central South University Changsha 410013, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) play a vital role in the progression of several cancers, including nasopharyngeal carcinoma (NPC). However, the mechanism of lncRNA involvement in the progression of NPC remains to be elucidated. Hence, we conducted in vivo and in vitro experiments to determine the molecular mechanism of FOXD1-AS1. We found that FOXD1-AS1 was over-expressed in NPC cells and tissues, and was significantly associated with poor survival rate in patients with NPC. We also found that FOXD1-AS1 promotes cellular proliferation, migration, invasion, and glycolysis, and inhibits apoptosis by upregulating the expression of FOXD1. Furthermore, FOXD1 could transcriptionally up-regulate the expression of key glycolytic genes to promote the glycolysis levels of NPC. The identified FOXD1-AS1 may serve as a potential prognostic biomarker and therapeutic target for patients with NPC.

Indexed as

FOXD1FOXD1-AS1glycolysisnasopharyngeal carcinomaprogression

Identifiers

PMID33294261
PMCPMC7716144
OpenAlexW3112000710

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.