Evidence map›Paper›PMID 41430250›Full record

ArticleCancer cell international2025

PTDSS1 serves as a prognostic biomarker of macrophage infiltration in pan-cancer and promotes hepatocellular carcinoma malignant phenotypes.

Chenlu Lan, Zuyin Wan, Haifei Qin, Haixiang Xie, Yu Chen, Chongjiu Qin, Zhongliu Wei, Yongguang Wei, Xin Zhou, Wei Qin and 2 more

Abstract read
In one paragraph

Article in Cancer cell international, 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

12 authors.

Chenlu Lan *Department of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Zuyin Wan *Department of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Haifei Qin *Department of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Haixiang XieDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Yu ChenDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Chongjiu QinDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Zhongliu WeiDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Yongguang WeiDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Xin ZhouDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Wei QinDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China.
Guangzhi ZhuDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China. zhuguangzhi0792@hotmail.com.
Tao PengDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi Zhuang Autonomous Region, People's Republic of China. pengtaogmu@163.com.

Funding

Innovation Project of Guangxi Graduate Education YCSW2025252National Natural Science Foundation of China 82360465National Natural Science Foundation of China 82560579National Postdoctoral Researcher Funding Program GZC20230583Natural Science Foundation of Guangxi Zhuang Autonomous Region 2024GXNSFDA010029Young and Middle-aged Scientific Research Capacity Enhancement Project 2024KY0128
6 · The paper itself

Abstract

backgroundPhosphatidylserine synthase 1 (PTDSS1) inhibitor has been developed and shows promising anti-tumor effect, but existing studies about PTDSS1 remain limited in cancer.

methodsThis study preliminarily analyzed the differential expression, prognostic significance, copy number variation, methylation level, co-expression network and immune correlation of PTDSS1 in pan-cancer. Furthermore, we collected tumor samples and corresponding clinical information of 74 hepatocellular carcinoma (HCC) patients from the First Hospital of Guangxi Medical University (Guangxi cohort) to validate PTDSS1 expression and prognostic value. In vitro experiments were performed to investigate the effect of PTDSS1 knockdown on the malignant phenotypes of HCC cell lines.

resultsThis study identified that PTDSS1 was significantly upregulated across most cancer types and associated with poor prognosis of seven cancer types. Copy number amplification and hypermethylation of PTDSS1 may drive its upregulation. Furthermore, PTDSS1 exhibited a positive correlation with macrophage in various cancers, co-expression network and functional enrichment analysis revealed that PTDSS1 may involve in cell division, cell cycle, DNA repair, cell proliferation, cell migration, cell growth, immune response and WNT signaling pathway. Regarding HCC, the differential expression and prognostic significance of PTDSS1 were verified by Guangxi cohort, single cell sequencing analysis revealed PTDSS1 located in tumor cell and macrophages. In vitro experiments demonstrated that PTDSS1 knockdown suppressed the proliferation, migration, invasion of HCC cells and promoted macrophage repolarization towards the M1 phenotype.

conclusionsPTDSS1 serves as a diagnostic and prognostic biomarker associated with macrophage infiltration, and may be a promising therapeutic target.

Indexed as

HCCPan-cancerPhosphatidylserinePTDSS1

Identifiers

PMID41430250
PMCPMC12752422

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 OpenQuestion graph.