Evidence map›Paper›PMID 32059763›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2020

RBP EIF2S2 Promotes Tumorigenesis and Progression by Regulating MYC-Mediated Inhibition via FHIT-Related Enhancers.

Jiwei Zhang, Shengli Li, Ling Zhang, Juan Xu, Mingxu Song, Tingting Shao, Zhaohui Huang, Yongsheng Li

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 52 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Jiwei ZhangThe MOE Key Laboratory for Standardization of Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China. Electronic address: joveus1024@gmail.com.
Shengli LiDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX 77030, USA.
Ling ZhangCollege of Life Science, Zhejiang Chinese Medical University, Hangzhou 310009, China.
Juan XuKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou 571199, China; College of Biomedical Information and Engineering, Hainan Medical University, Haikou 571199, China; College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang 150081, China.
Mingxu SongWuxi Cancer Institute, Affiliated Hospital of Jiangnan University, 200 Huihe Road, Wuxi Shi, Jiangsu Province 214123, China.
Tingting ShaoCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang 150081, China.
Zhaohui HuangWuxi Cancer Institute, Affiliated Hospital of Jiangnan University, 200 Huihe Road, Wuxi Shi, Jiangsu Province 214123, China. Electronic address: hzhwxsy@126.com.
Yongsheng LiKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou 571199, China; College of Biomedical Information and Engineering, Hainan Medical University, Haikou 571199, China; College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang 150081, China. Electronic address: liyongsheng@hainmc.edu.cn.
Harbin Medical University · CNWuxi Fourth People's Hospital · CNShanghai University of Traditional Chinese Medicine · CNThe University of Texas Health Science Center at Houston · USZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-binding proteins (RBPs) play fundamental roles in cancer; however, we still lack knowledge about to what extent RBPs are dysregulated, as well as about perturbed signaling pathways in cancer. In this study, we integrated analysis of multidimensional data across >10,000 cancer patients and >1,000 cell lines. We identified a top candidate RBP: eukaryotic translation initiation factor 2 subunit beta (EIF2S2). EIF2S2 is highly expressed in tumors and is associated with malignant features as well as patient prognosis. Functional assays performed in cancer cells revealed that EIF2S2 promotes cancer cell proliferation, migration, and invasion in vitro as well as tumor growth and metastasis in vivo. Mechanistic investigations further demonstrated that EIF2S2 promotes tumorigenesis and progression by directly binding to a long non-coding RNA, LINC01600, which physically interacts with the MYC protein and increases its stability. Interestingly, we revealed that the EIF2S2-LINC01600-MYC axis can activate the Wnt/β-catenin pathway by inhibiting the activity of FHIT-related enhancers and FHIT expression. Finally, EIF2S2 knockdown combined with oxaliplatin treatment could be a potential combination therapy in cancer. Our integrated analysis provided detailed knowledge of the function of the EIF2S2-LINC01600-MYC axis, which will facilitate the development of rational combination therapies for cancer.

Indexed as

Cell Line, TumorCell MovementCell ProliferationCell SurvivalColorectal NeoplasmsDisease ProgressionEukaryotic Initiation Factor-2Gene Expression Regulation, NeoplasticGene Knockout TechniquesHCT116 CellsHT29 CellsHumansOxaliplatinProtein StabilityProto-Oncogene Proteins c-mycRNA, Long NoncodingEukaryotic Initiation Factor-2MYC protein, humanOxaliplatinProto-Oncogene Proteins c-mycRNA, Long NoncodingEIF2S2gastrointestinal cancerlong non-coding RNARNA-binding proteinWnt pathway

Identifiers

PMID32059763
PMCPMC7132626
OpenAlexW3005340795

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.