Evidence map›Paper›PMID 38216684›Full record

ArticleNature nanotechnology2024

Nanoreceptors promote mutant p53 protein degradation by mimicking selective autophagy receptors.

Xiaowan Huang, Ziyang Cao, Jieying Qian, Tao Ding, Yanxia Wu, Hao Zhang, Suqin Zhong, Xiaoli Wang, Xiaoguang Ren, Wang Zhang and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature nanotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
17.4field-weighted citation impact, top 1% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Supramolecular Degraders: An Emerging Paradigm in Targeted Protein Degradation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. LFPM inhibition of RING1-mediated p53Cell death and differentiation · 2026
    Article
  6. ESCRT-Mimetic Nanodegrader Targets STING for Anti-Inflammatory Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Insights gained from single-cell sequencing analysis of ischemic stroke.Frontiers in cell and developmental biology · 2026
    Review
  13. Review
  14. Mutant p53 regulates reversible subtype plasticity in pancreatic cancer.Cellular and molecular life sciences : CMLS · 2025
    Article
  15. Review
  16. Targeted Degradation Technologies Utilizing Autophagy.International journal of molecular sciences · 2025
    Review
  17. Review
  18. Article
  19. Review
  20. Review
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

16 authors at 5 institutions in 1 country.

Xiaowan Huang *School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, People's Republic of China.ORCID 0009-0006-9701-0855
Ziyang Cao *Department of General Surgery, Guangzhou Digestive Disease Center, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, People's Republic of China.ORCID 0000-0003-0661-4022
Jieying Qian *School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, People's Republic of China.
Tao DingSchool of Medicine, South China University of Technology, Guangzhou, People's Republic of China.
Yanxia WuMolecular Cancer Research Center, School of Medicine, Sun Yat-Sen University, Shenzhen, People's Republic of China.
Hao ZhangSchool of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, People's Republic of China.
Suqin ZhongSchool of Medicine, South China University of Technology, Guangzhou, People's Republic of China.
Xiaoli WangSchool of Medicine, South China University of Technology, Guangzhou, People's Republic of China.
Xiaoguang RenSchool of Medicine, South China University of Technology, Guangzhou, People's Republic of China.
Wang ZhangSchool of Medicine, South China University of Technology, Guangzhou, People's Republic of China.
Youcui XuMedical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, People's Republic of China.
Guangyu YaoBreast Center, Nanfang Hospital, Southern Medical University, Guangzhou, People's Republic of China.ORCID 0000-0002-3406-7612
Xingwu WangMolecular Cancer Research Center, School of Medicine, Sun Yat-Sen University, Shenzhen, People's Republic of China.ORCID 0000-0002-2457-8726
Xianzhu YangSchool of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, People's Republic of China. yangxz@scut.edu.cn.ORCID 0000-0002-1006-0950
Longping WenMedical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, People's Republic of China. lpwen@ustc.edu.cn.ORCID 0000-0003-0384-4578
Yunjiao ZhangSchool of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, People's Republic of China. zhangyunjiao@scut.edu.cn.ORCID 0000-0002-6465-7488
South China University of Technology · CNSun Yat-sen University · CNGuangdong Academy of Medical Sciences · CNGuangzhou First People's Hospital · CNNanfang Hospital · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32071398National Natural Science Foundation of China (National Science Foundation of China) 32171375National Natural Science Foundation of China (National Science Foundation of China) 52203163National Natural Science Foundation of China (National Science Foundation of China) 82150118National Natural Science Foundation of China (National Science Foundation of China) 82202305National Natural Science Foundation of China (National Science Foundation of China) T2222014National Natural Science Foundation of China (National Science Foundation of China) U22A20156
6 · The paper itself

Abstract

In some cancers mutant p53 promotes the occurrence, development, metastasis and drug resistance of tumours, with targeted protein degradation seen as an effective therapeutic strategy. However, a lack of specific autophagy receptors limits this. Here, we propose the synthesis of biomimetic nanoreceptors (NRs) that mimic selective autophagy receptors. The NRs have both a component for targeting the desired protein, mutant-p53-binding peptide, and a component for enhancing degradation, cationic lipid. The peptide can bind to mutant p53 while the cationic lipid simultaneously targets autophagosomes and elevates the levels of autophagosome formation, increasing mutant p53 degradation. The NRs are demonstrated in vitro and in a patient-derived xenograft ovarian cancer model in vivo. The work highlights a possible direction for treating diseases by protein degradation.

Indexed as

AutophagyTumor Suppressor Protein p53Cell Line, TumorHumansLipidsMutant ProteinsPeptidesProteolysisLipidsMutant ProteinsPeptidesTumor Suppressor Protein p53

Identifiers

PMID38216684
OpenAlexW4390789317

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.