Evidence map›Paper›PMID 40890114›Full record

ArticleCell death & disease2025

MAP3K13-232aa encoded by circMAP3K13 enhances cisplatin-induced pyroptosis by directly binding to IKKα in gastric adenocarcinoma.

Kaining Du, Xiaojing Zhang, Ying Qin, Huizhen Ma, Chuhan Bing, Shiqi Deng, Yang Chen, Jiequan Qin, Shanshan Chang, Siyu Xiao and 10 more

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
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  5. 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

20 authors.

Kaining Du *Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Xiaojing Zhang *Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.ORCID http://orcid.org/0000-0002-0595-3500
Ying Qin *Department of Gastrointestinal Surgery, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, Guangdong, PR China.
Huizhen MaGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Chuhan BingGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Shiqi DengGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.ORCID http://orcid.org/0000-0002-2128-1521
Yang ChenGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Jiequan QinGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Shanshan ChangGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Siyu XiaoGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Lehua PengGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Xiaoya XieGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Xianling FengGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Xianli FuDepartment of Pathology, Shenzhen University General Hospital, Shenzhen, Guangdong, PR China.
Yanjie WeiCenter for High Performance Computing, Shenzhen Institutes of Advanced Technology, Shenzhen, Guangdong, PR China.ORCID http://orcid.org/0000-0002-4791-7540
Xinmin FanGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Hassan AshktorabDepartment of Medicine and Cancer Center, Howard University, College of Medicine, Washington, DC, USA.
Duane SmootDepartment of Medicine, Meharry Medical Center, Nashville, TN, USA.
Zhe JinGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China.
Yin PengGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Department of Pathology, Shenzhen University Health Science Center, Shenzhen, Guangdong, PR China. ypeng@szu.edu.cn.ORCID http://orcid.org/0000-0001-7524-7508

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82172946, 82173290 and 82273029
6 · The paper itself

Abstract

Gastric cancer (GC) is one of the most common and lethal malignancies in developing countries, with particularly high prevalence in China. Circular RNAs (circRNAs) have garnered increasing attention for their roles in disease pathogenesis. While circRNAs can be translated, there have been few investigations into the biological functions of "translatable circRNAs" in the initiation and progression of gastric adenocarcinoma. In this study, we identified a circRNA, circMAP3K13, which inhibits the proliferation and migration of GC cells. CircMAP3K13 was found to encode a previously unreported 26 kDa protein, designated MAP3K13-232aa. Mechanistically, MAP3K13-232aa binds directly to the kinase domain of IKKα and enhances its activity, thereby promoting NF-κB signaling. This activation leads to upregulation of NLRP3 and increased cisplatin-induced pyroptosis in GC cells. Moreover, MAP3K13-232aa enhances pyroptosis and reduces tumorigenicity and metastasis in vivo. Taken together, both circMAP3K13 and its encoded protein MAP3K13-232aa represent potential therapeutic targets in GC.

Indexed as

AdenocarcinomaCisplatinI-kappa B KinasePyroptosisRNA, CircularStomach NeoplasmsAnimalsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansMiceMice, Inbred BALB CMice, NudeNF-kappa BCHUK protein, humanCisplatinI-kappa B KinaseNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinRNA, Circular

Identifiers

PMID40890114
PMCPMC12402440

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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.