Evidence map›Paper›PMID 39592671›Full record

ArticleScientific reports2024

eEF2K as an important kinase associated with cancer survival and prognosis.

Nan Wang, Li-Lan Cen, Zhe Tian, Miao-Miao An, Qian Gu, Xin-Hong Zhou, Yi-He Zhang, Lucas Liu, Jun Zhang, Di Yang and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A Covalent PFKL Activator Suppresses Tumor Growth.bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
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.

Nan Wang *The Second Surgical Department of Breast Cancer, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, 30071, China.
Li-Lan Cen *Key laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Zhe Tian *Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Miao-Miao AnKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Qian GuKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Xin-Hong ZhouKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Yi-He ZhangKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Lucas LiuAtkins Academic & Technology High School, Winston-Salem, NC, 27101, USA.
Jun ZhangDepartment of Neurosurgery, Peking University International Hospital, Beijing, 102206, China.
Di YangKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Yong-Zhi HuangKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China.
Xi-Dai LongKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China. longxidai@163.com.
Qian YangKey laboratory of molecular pathology in Tumors of Guangxi Higher Education Institutions, Department of Pathology, the Affiliated Hospital of Youjiang Medical University for Nationalities, Baise City, 533000, Guangxi Zhuang Autonomous Region, China. yangqian@ymun.edu.cn.

Funding

2023 Self-funded research project of Health Commission of Autonomous Region Z-A20230026Foundation for Bose Talent Highland 2020-3-2Foundation for Building Projects of Guangxi Bagui Scholars 2024Foundation for Medical High-level Academic Leaders Guiweikejiaofa [2020]-15Foundation of Baise city Scientific Research & Technology Development Plan BS20193220Foundation of Baise city Scientific Research & Technology Development Plan BS20224120Foundation of Graduate Innovation of the Affiliated Hospital of Youjiang Medical University for Nationality YXCXJH2024003Foundation of Guangxi Graduate Education Innovation Plan JGY2020165Introduced Talents and Doctoral start-up funding from Tianjin Medical University Cancer Institute and Hospital B1617Key Laboratory of Molecular Pathology (Hepatobiliary Diseases) of Guangxi and the Key La-boratory of Tumor Molecular Pathology of Guangxi Colleges & Universities [2022]-NO.21Natural Science Foundation of Guangxi Zhuang Autonomous Region 2019AC20043Research Foundation of the Affiliated Hospital of Youjiang Medical University for Nationality R20196304
6 · The paper itself

Abstract

Eukaryotic Elongation Factor 2 Kinase (eEF2K), a member of the α-kinase family, services as a crucial negative regulator of protein synthesis, particularly under conditions of cellular stress. A pan-cancer analysis of eEF2K expression, genetic variants, and clinical relevance across multiple tumor types was performed using data from the Cancer Genome Atlas (TCGA) and GEO. Our findings suggest that eEF2K has dual roles in cancer progression, with its expression correlating with patient prognosis. Significant phosphorylation of eEF2 at T57, Y434, and T59 was observed, which may regulate protein synthesis during stress. The elevated T59 phosphorylation in COAD, despite the low eEF2K expression, indicates that this may be regulated by alternative kinases, such as AMPK or mTOR. This suggests that compensatory mechanisms may be involved. In addition to modulating eEF2 phosphorylation, eEF2K is involved in a number of other processes, including peptidyl-serine phosphorylation, the G2/M transition, and the MAPK cascade. The protein products of eEF2K are capable of localizing to the nucleus, cytoplasm, and cytosol, where they bind to a range of proteins, including ATP and calcium ions. These findings provide novel insights into the role of eEF2K in cancer biology and suggest that the targeting of eEF2K and eEF2 phosphorylation may offer promising therapeutic strategies.

Indexed as

Elongation Factor 2 KinaseNeoplasmsGene Expression Regulation, NeoplasticHumansPhosphorylationPrognosisEEF2K protein, humanElongation Factor 2 KinaseCancereEF2KPan-cancer analysisPhosphorylationPrognosis

Identifiers

PMID39592671
PMCPMC11599947

What Socratic holds

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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 Socratic graph.