Evidence map›Paper›PMID 35209949›Full record

ArticleJournal of experimental & clinical cancer research : CR2022

Long noncoding RNA LINC00930 promotes PFKFB3-mediated tumor glycolysis and cell proliferation in nasopharyngeal carcinoma.

Baoyu He, Hongli Pan, Fengque Zheng, Saiqiong Chen, Qingli Bie, Jinghe Cao, Rou Zhao, Jing Liang, Li Wei, Jianchao Zeng and 13 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.0field-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

27 citing papers in PubMed, 34 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

23 authors at 4 institutions in 1 country.

Baoyu He *Department of Laboratory Medicine, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China. hebaoyu99@sina.com.ORCID http://orcid.org/0000-0002-5476-8651
Hongli Pan *Medical Science Laboratory, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Fengque Zheng *Department of Obstetrics and Gynecology, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Saiqiong ChenDepartment of Obstetrics and Gynecology, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Qingli BieDepartment of Laboratory Medicine, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Jinghe CaoDepartment of Reproductive Center, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Rou ZhaoDepartment of Laboratory Medicine, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Jing LiangDepartment of Laboratory Medicine, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Li WeiDepartment of Laboratory Medicine, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Jianchao ZengMedical Science Laboratory, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Hui LiDepartment of Oncology, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Xing CuiDepartment of Otolaryngology, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Yixuan DingDepartment of Pathology, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Wei ChaoMedical Science Laboratory, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Tiantian XiangExperimental Center of Medical Science, Guangxi Medical University, Nanning, Guangxi, China.
Yuhe ChengDepartment of Oncology, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Gui QiuMedical Science Laboratory, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Shishun HuangMedical Science Laboratory, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China.
Libo TangMedical Science Laboratory, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Jiansheng ChangDepartment of Oncology, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Delan LuoDepartment of Gastroenterology, the First People's Hospital of Neijiang City, Neijiang, Sichuan, China.
Jie YangDepartment of Hematology, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi, China. 458805114@qq.com.
Bin ZhangDepartment of Laboratory Medicine, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China. zhb861109@163.com.
Fourth Affiliated Hospital of Guangxi Medical University · CNAffiliated Hospital of Jining Medical University · CNGuangxi Medical University · CNNeijiang Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic reprogramming is a hallmark of cancer. However, the roles of long noncoding RNAs (lncRNAs) in cancer metabolism, especially glucose metabolism remain largely unknown.

resultsIn this study, we identified and functionally characterized a novel metabolism-related lncRNA, LINC00930, which was upregulated and associated with tumorigenesis, lymphatic invasion, metastasis, and poor prognosis in nasopharyngeal carcinoma (NPC). Functionally, LINC00930 was required for increased glycolysis activity and cell proliferation in multiple NPC models in vitro and in vivo. Mechanistically, LINC00930 served as a scaffold to recruit the RBBP5 and GCN5 complex to the PFKFB3 promoter and increased H3K4 trimethylation and H3K9 acetylation levels in the PFKFB3 promoter region, which epigenetically transactivating PFKFB3, and thus promoting glycolytic flux and cell cycle progression. Clinically, targeting LINC00930 and PFKFB3 in combination with radiotherapy induced tumor regression.

conclusionsCollectively, LINC00930 is mechanistically, functionally and clinically oncogenic in NPC. Targeting LINC00930 and its pathway may be meaningful for treating patients with NPC.

Indexed as

AnimalsCell Line, TumorCell ProliferationDisease Models, AnimalFemaleGlycolysisHumansMiceNasopharyngeal NeoplasmsOncogenesPhosphofructokinase-2RNA, Long NoncodingTransfectionPFKFB3 protein, mousePhosphofructokinase-2RNA, Long NoncodingGlycolysisLINC00930Nasopharyngeal carcinomaPFKFB3RBBP5/GCN5

Identifiers

PMID35209949
PMCPMC8867671
OpenAlexW4213434601

What OpenQuestion holds

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LicenceCC BY
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.