Evidence map›Paper›PMID 40508020›Full record

ArticleInternational journal of molecular sciences2025

PBX3-HMGCR Axis Promotes Hepatocellular Carcinoma Progression Through Enhancing De Novo Cholesterol Biosynthesis.

Xia Zhang, Li Qiu, Lei Zhang, Wenfang Li, Debing Xiang, Jian Wang, Shourong Wu, Vivi Kasim

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Xia ZhangKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.
Li QiuKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.
Lei ZhangKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.ORCID 0000-0002-8239-5602
Wenfang LiKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.ORCID 0000-0003-0436-4277
Debing XiangKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.ORCID 0009-0002-4258-2224
Jian WangKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.
Shourong WuKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.ORCID 0000-0001-9650-5465
Vivi KasimKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Department of Oncology, Chongqing University Jiangjin Hospital, Chongqing University, Chongqing 400044, China.ORCID 0000-0001-9182-8230

Funding

National Natural Science Foundation of China 32270778National Natural Science Foundation of China 82173029the Talent Project of Chongqing University Jiangjin Hospital 2024LJXM005
6 · The paper itself

Abstract

Tumor cells alter lipid metabolic pathways to meet their demands for energy and membrane biosynthesis. Despite its crucial role in tumor cell growth, survival, and metastasis, the mechanisms underlying tumor cell lipid metabolic reprogramming remain poorly understood. Pre-B-cell leukemia transcription factor 3 (PBX3), a member of the PBX family, could promote tumorigenesis; however, whether it is involved in tumor lipid metabolic reprogramming remains unknown. Herein, we found that PBX3 significantly promotes tumor growth by enhancing lipid accumulation in HCC cells. By assessing the effect of PBX3 on the expression levels of lipid metabolism-related genes, we found that PBX3 could positively regulate the expression of 3-hydroxy-3-methylglutaryl CoA reductase (HMGCR), a rate-limiting enzyme in the cholesterol biosynthesis pathway. Mechanistically, we revealed that PBX3 could directly bind to the -167/-151 region of

Indexed as

Carcinoma, HepatocellularCholesterolHomeodomain ProteinsHydroxymethylglutaryl CoA ReductasesLiver NeoplasmsProto-Oncogene ProteinsAnimalsCell Line, TumorCell ProliferationDisease ProgressionGene Expression Regulation, NeoplasticHumansLipid MetabolismMicePromoter Regions, GeneticCholesterolHMGCR protein, humanHomeodomain ProteinsHydroxymethylglutaryl CoA Reductasesproto-oncogene protein Pbx3Proto-Oncogene Proteinscholesterol biosynthesisHMGCRlipid metabolismPBX3tumor metabolic reprogramming

Identifiers

PMID40508020
PMCPMC12154334

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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.