Evidence map›Paper›PMID 26942880›Full record

ArticleOncotarget2016

4EGI-1 induces apoptosis and enhances radiotherapy sensitivity in nasopharyngeal carcinoma cells via DR5 induction on 4E-BP1 dephosphorylation.

Weiyuan Wang, Jiao Li, Qiuyuan Wen, Jiadi Luo, Shuzhou Chu, Lingjiao Chen, Zhenzhen Qing, Guiyuan Xie, Lina Xu, Mohannad Ma Alnemah and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  8. FeJournal of translational medicine · 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

13 authors at 2 institutions in 1 country.

Weiyuan WangDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jiao LiDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qiuyuan WenDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jiadi LuoDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Shuzhou ChuDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Lingjiao ChenDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhenzhen QingDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Guiyuan XieDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Lina XuDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Mohannad Ma AlnemahDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Meirong LiDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Songqing FanDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hongbo ZhangDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Second Xiangya Hospital of Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The eIF4F complex regulated by a various group of eIF4E-binding proteins (4E-BPs) can initial the protein synthesis. Small molecule compound 4EGI-1, an inhibitor of the cap-dependent translation initiation through disturbing the interaction between eIF4E and eIF4G which are main elements of the eIF4E complex, has been reported to suppress cell proliferation by inducing apoptosis in many types of cancer. And death receptor 5 (DR5) is a major component in the extrinsic apoptotic pathway. However, the correlation among 4EGI-1, DR5 and 4E-BPs have not been discovered in NPC now. Therefore, we intend to find out the effect of 4EGI-1 on the apoptosis process of NPC and the relationship among 4EGI-1, DR5 and 4E-BPs. Our results revealed a significant down regulation of DR5 expression in NPC tissues, which inversely correlated with lymph node metastasis status and clinical stages. Depressed DR5 expression was an independent biomarker for poor prognosis in NPC, and elevated DR5 expression showed longer overall survival time in 174 NPC patients. Besides, 4EGI-1 induced apoptosis in NPC cells through the DR5-caspase-8 axis on 4E-BP1 and eIF4E dephosphorylation exerting positive influence on their anti-tumor activities. The induction of DR5 also sensitized NPC cells to radiotherapy, and the SER was 1.195. These results establish the death receptor pathway as a novel anticancer mechanism of eIF4E/eIF4G interaction inhibitor in NPC.

Indexed as

Adaptor Proteins, Signal TransducingAdultApoptosisBlotting, WesternCell Cycle ProteinsCell Line, TumorEpitheliumFemaleHumansHydrazonesImmunohistochemistryMaleMiddle AgedNasopharyngeal NeoplasmsPhosphoproteinsPhosphorylation4EGI-1 compoundAdaptor Proteins, Signal TransducingCell Cycle ProteinsEIF4EBP1 protein, humanHydrazonesPhosphoproteinsReceptors, TNF-Related Apoptosis-Inducing LigandThiazoles4EGI-1apoptosisDR5nasopharyngeal carcinomaradiotherapy

Identifiers

PMID26942880
PMCPMC5008318
OpenAlexW2291383980

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.