Evidence map›Paper›PMID 42225931›Full record

ArticleNPJ precision oncology2026

Fuzuloparib enhances radiosensitivity of gain-of-function mutant p53 R273H NSCLC by promoting SLC7A11/GSH/GPX4 axis mediated ferroptosis.

Mengjia Wu, Chaoyuan Pu, Wanxuan Weng, Fengmin Yin, Lei Zhang, Chenggang Xu, Mingjian Li, Chuanhui Cao, Wei Hu

Abstract read
In one paragraph

Article in NPJ precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Mengjia Wu *Department of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Chaoyuan Pu *Department of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Wanxuan Weng *Fuling Hospital of Chongqing University, Chongqing University, Chongqing, China.
Fengmin YinDepartment of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Lei ZhangDepartment of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Chenggang XuDepartment of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Mingjian LiDepartment of Interventional Radiology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Chuanhui CaoDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China. caochuan@smu.edu.cn.
Wei HuDepartment of Oncology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China. huwei@zmu.edu.cn.

Funding

Guizhou Provincial Health Commission, Science and Technology Foundation Project 2024GZWJKJXM1315National Natural Science Foundation of China Nos. 82460579Special project of Science and Technology Research of Traditional Chinese Medicine and ethnic Medicine of Guizhou Traditional Chinese Medicine Administration QZYY-2024-021
6 · The paper itself

Abstract

Radiotherapy is a crucial therapeutic approach for the management of non-small cell lung cancer (NSCLC). Nevertheless, the radioresistance of NSCLC, particularly in cases involving the gain-of-function mutant p53, substantially limits its efficacy. According to recent research, mutant p53 R273H can recruit poly (ADP-ribose) polymerase (PARP)-1 on replicating DNA to promote tumor survival. Whether mutant p53 R273H-mediated radioresistance is related to the interaction between mutant p53 R273H and PARP1, and if PARP1 inhibitors (PARPi) can increase the radiosensitivity of mutant p53 R273H-expressing tumors have not been explored. Through in vitro and in vivo experiments, we determined that mutant p53 R273H promotes radioresistance in NSCLC by partially inhibiting ferroptosis through the SLC7A11/GSH/GPX4 axis, independently of PARP1, whereas FZ counteracts this effect by partially blocking the same axis to promote ferroptosis, presenting a potential novel strategy for treating NSCLC patients with gain-of-function mutant p53 R273H.

Identifiers

PMID42225931
PMCPMC13526843

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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.