Evidence map›Paper›PMID 41484250›Full record

ArticleCommunications biology2026

The p53 R181C mutation accumulates through impaired deacetylation by Sirt1 and facilitates tumor development.

Erli Wang, Liangzi Cao, Wendong Guo, Xiang Dong, Wanying Zhang, Xiaowen Zhang, Zhuo Wang, Xia Chen, Aicun Li, Yu Zou and 12 more

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

22 authors.

Erli Wang *Clinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Liangzi Cao *Clinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Wendong GuoClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Xiang DongClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Wanying ZhangClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Xiaowen ZhangClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Zhuo WangClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Xia ChenClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Aicun LiClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Yu ZouClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Shikun LiClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Kedian ChenClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Han SuClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Sunrun CaoClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Ning DuClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China.
Pingyuan WangCardiovascular Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Paul M HwangCardiovascular Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-5976-7834
Xiangsheng LiuZhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, Zhejiang Province, China. liuxs@him.cas.cn.ORCID http://orcid.org/0000-0002-5719-2838
Xiaoyu SongClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China. xysong@cmu.edu.cn.ORCID http://orcid.org/0000-0002-6606-327X
Hongde XuClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China. HdXu@cmu.edu.cn.ORCID http://orcid.org/0000-0002-8026-2443
Jingwei LiuClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China. jwliu@cmu.edu.cn.ORCID http://orcid.org/0000-0002-4589-8147
Liu CaoClinical Translational Research Center, Shengjing Hospital, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province, China. lcao@cmu.edu.cn.ORCID http://orcid.org/0000-0001-6471-1993

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Li-Fraumeni Syndrome (LFS) is linked to mutations in the p53 gene and is characterized by autosomal dominant early-onset familial cancer susceptibility. The p53R181C mutation is one of the earliest described mutations associated with early-onset familial hereditary breast cancer. Highly stable mutant p53 protein is often a prerequisite for tumor initiation and progression, but the pathways leading to p53R181C accumulation and carcinogenesis are not understood. Here, we found that p53 R181C mutation decreases the interaction of p53 with the Sirt1 deacetylase, resulting in increased p53 K382 acetylation and inhibition of MDM2-mediated ubiquitination and degradation of p53. Moreover, the R181C mutation leads to "loss-of-function" of transcriptional regulating tumor suppressor genes like p21, bax, and PUMA as well as "gain-of-function" of transcriptional regulating tumor promoting genes of PIK3CA, SHC1, SRC and PAK4. This dysregulation promotes genomic instability, enabling cancer cells to evade cell cycle control, senescence and apoptosis, thus facilitating tumor development. Our findings unraveled the mechanism by which the p53R181C mutant protein accumulates and facilitates tumor development.

Indexed as

CarcinogenesisLi-Fraumeni SyndromeMutationSirtuin 1Tumor Suppressor Protein p53AcetylationAnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansSIRT1 protein, humanSirtuin 1TP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID41484250
PMCPMC12881656

What OpenQuestion 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 OpenQuestion graph.