Evidence map›Paper›PMID 37624574›Full record

ReviewCell biochemistry and biophysics2023

Inhibitors Targeting the F-BOX Proteins.

Yalnaz Naseem, Chaofeng Zhang, Xinyi Zhou, Jianshu Dong, Jiachong Xie, Huimin Zhang, Clement Agboyibor, YueFeng Bi, Hongmin Liu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell biochemistry and biophysics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Versatile JMJD proteins: juggling histones and much more.Trends in biochemical sciences · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. 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

9 authors at 2 institutions in 2 countries.

Yalnaz Naseem *School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Chaofeng Zhang *School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Xinyi ZhouSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Jianshu Dong *School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China. jdong@zzu.edu.cn.
Jiachong XieSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Huimin ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Clement AgboyiborSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
YueFeng BiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China. zzubyf@126.com.
Hongmin LiuInstitute of Drug Discovery and Development, Zhengzhou University, Zhengzhou, 450001, China. liuhm@zzu.edu.cn.
Zhengzhou University · CNMinistry of Education · NZ

Funding

National Key Research Program 2018YFE0195100National Natural Science Foundation of China 31900913National Natural Science Foundation of China NOs. 31900913, 82020108030, 81773562, 81703326 and 81973177The postgraduate-education research programme of Zhengzhou university in 2021 YJSJY202159
6 · The paper itself

Abstract

F-box proteins are involved in multiple cellular processes through ubiquitylation and consequent degradation of targeted substrates. Any significant mutation in F-box protein-mediated proteolysis can cause human malformations. The various cellular processes F-box proteins involved include cell proliferation, apoptosis, invasion, angiogenesis, and metastasis. To target F-box proteins and their associated signaling pathways for cancer treatment, researchers have developed thousands of F-box inhibitors. The most advanced inhibitor of FBW7, NVD-BK M120, is a powerful P13 kinase inhibitor that has been proven to bring about apoptosis in cancerous human lung cells by disrupting levels of the protein known as MCL1. Moreover, F-box Inhibitors have demonstrated their efficacy for treating certain cancers through targeting particular mutated proteins. This paper explores the key studies on how F-box proteins act and their contribution to malignancy development, which fabricates an in-depth perception of inhibitors targeting the F-box proteins and their signaling pathways that eventually isolate the most promising approach to anti-cancer treatments.

Indexed as

F-Box ProteinsNeoplasmsCell Cycle ProteinsF-Box-WD Repeat-Containing Protein 7HumansProteolysisUbiquitinationUbiquitin-Protein LigasesCell Cycle ProteinsF-Box ProteinsF-Box-WD Repeat-Containing Protein 7Ubiquitin-Protein Ligasescancer progressionE3 ligaseF-box proteinsmall molecule inhibitorsubstrateUbiquitin

Identifiers

PMID37624574
OpenAlexW4386154243

What Socratic 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 Socratic graph.