Evidence map›Paper›PMID 37596667›Full record

ArticleCell communication and signaling : CCS2023

NEK8 regulates colorectal cancer progression via phosphorylating MYC.

Beibei Cao, Kailun Zhang, Changjie Pan, Yifei Dong, Feng Lu

Abstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2023. 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.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. The NIMA-related kinase family and cancer.Frontiers in oncology · 2025
    Review
  7. Mutational insights andFrontiers in bioinformatics · 2025
    Article
  8. Signaling, cancer cell plasticity, and intratumor heterogeneity.Cell communication and signaling : CCS · 2024
    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

5 authors.

Beibei CaoDepartment of Breast Surgery, Henan Provincial People's Hospital, Zhengzhou City, China.
Kailun ZhangZhengzhou University People's Hospital, Zhengzhou City, China.
Changjie PanZhengzhou University People's Hospital, Zhengzhou City, China.
Yifei DongZhengzhou University People's Hospital, Zhengzhou City, China.
Feng LuDepartment of Breast Surgery, Henan Provincial People's Hospital, Zhengzhou City, China. 9362159@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiotherapy and chemotherapy remain the mainstay of treatment for colorectal cancer (CRC), although their efficacy is limited. A detailed understanding of the molecular mechanisms underlying CRC progression could lead to the development of new therapeutic strategies. Although it has been established that MYC signaling is dysregulated in various human cancers, direct targeting MYC remains challenging due to its "undruggable" protein structure. Post-translational modification of proteins can affect their stability, activation, and subcellular localization. Hence, targeting the post-translational modification of MYC represents a promising approach to disrupting MYC signaling. Herein, we revealed that NEK8 positively regulates CRC progression by phosphorylating c-MYC protein at serine 405, which exhibited enhanced stability via polyubiquitination. Our findings shed light on the role of NEK8/MYC signaling in CRC progression, offering a novel and helpful target for colorectal cancer treatment. Video Abstract.

Indexed as

Colorectal NeoplasmsNIMA-Related KinasesProto-Oncogene Proteins c-mycHumansProtein Processing, Post-TranslationalSerineSignal TransductionNEK8 protein, humanNIMA-Related KinasesProto-Oncogene Proteins c-mycSerineColorectal cancerMYCNEK8

Identifiers

PMID37596667
PMCPMC10436496

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.