Evidence map›Paper›PMID 40107714›Full record

ArticleLife science alliance2025

TPX2 lactylation is required for the cell cycle regulation and hepatocellular carcinoma progression.

Shengzhi Liu, Jin Cai, Xiaoyu Qian, Junjiao Zhang, Yi Zhang, Xiang Meng, Mingjie Wang, Ping Gao, Xiuying Zhong

Abstract read
In one paragraph

Article in Life science alliance, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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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.

Shengzhi Liuhttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China.
Jin Caihttps://ror.org/045kpgw45 Medical Research Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China.ORCID 0009-0006-8427-7075
Xiaoyu Qianhttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China.
Junjiao Zhanghttps://ror.org/0530pts50 School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China.
Yi Zhanghttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China.
Xiang Menghttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China.
Mingjie Wanghttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China.
Ping Gaohttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China pgao2@ustc.edu.cn.ORCID 0000-0002-6930-7989
Xiuying Zhonghttps://ror.org/0530pts50 School of Medicine, South China University of Technology, Guangzhou, China zxywawj@ustc.edu.cn.ORCID 0000-0002-1616-1330

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting protein for Xklp2 (TPX2) is critical for mitosis and spindle assembly because of its control of Aurora kinase A (AURKA). However, the regulation of TPX2 activity and its subsequent effects on mitosis and cancer progression remain unclear. Here, we show that TPX2 is lactylated at K249 in hepatocellular carcinoma (HCC) tumour tissues and that this process is regulated by the lactylase CBP and the delactylase HDAC1. Lactate reduction via either shRNAs targeting lactate dehydrogenase A or the lactate dehydrogenase A inhibitor GSK2837808A decreases the level of TPX2 lactylation. Importantly, TPX2 lactylation is required for the cell cycle regulation and tumour growth. Mechanistically, TPX2 lactylation disrupts protein phosphatase 1 (PP1) binding to AURKA, enhances AURKA T288 phosphorylation, and facilitates the cell cycle progression. Overall, our study reveals a previously unappreciated role of TPX2 lactylation in regulating cell cycle progression and HCC tumorigenesis, exposing an important correlation between metabolic reprogramming and cell cycle regulation in HCC.

Indexed as

Carcinoma, HepatocellularCell Cycle ProteinsLiver NeoplasmsMicrotubule-Associated ProteinsNuclear ProteinsAnimalsAurora Kinase ACell CycleCell Line, TumorCell ProliferationDisease ProgressionHumansMiceMitosisPhosphorylationAURKA protein, humanAurora Kinase ACell Cycle ProteinsMicrotubule-Associated ProteinsNuclear ProteinsTPX2 protein, human

Identifiers

PMID40107714
PMCPMC11924114

What Socratic holds

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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.