Evidence map›Paper›PMID 33495903›Full record

ArticleHepatology international2021

S100P as a novel biomarker of microvascular invasion and portal vein tumor thrombus in hepatocellular carcinoma.

Lu-Nan Qi, Liang Ma, Fei-Xiang Wu, Yuan-Yuan Chen, Wan-Ting Xing, Zhi-Jun Jiang, Jian-Hong Zhong, Zu-Shun Chen, Wen-Feng Gong, Jia-Zhou Ye and 4 more

Abstract read
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In one paragraph

Article in Hepatology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  8. Prognostic Value of S100 Family mRNA Expression in Hepatocellular Carcinoma.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
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  11. Review
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  14. S100 Proteins in Fatty Liver Disease and Hepatocellular Carcinoma.International journal of molecular sciences · 2022
    Review
  15. [Research progress of microvascular invasion in hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
    Review
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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

14 authors at 4 institutions in 1 country.

Lu-Nan Qi *Department of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China. wangzhennuo@aliyun.com.ORCID http://orcid.org/0000-0003-0254-6982
Liang Ma *Department of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Fei-Xiang Wu *Department of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Yuan-Yuan ChenDepartment of Ultrasound, First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China.
Wan-Ting XingDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Zhi-Jun JiangDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Jian-Hong ZhongDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Zu-Shun ChenDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Wen-Feng GongDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Jia-Zhou YeDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Hong-Hao LiKey Laboratory of Early Prevention and Treatment for Regional High Frequency Tumor, Ministry of Education, Nanning, 530021, Guangxi, China.
Jin-Jie ShangJiangsu Key Laboratory for Microbes and Functional Genomics, College of Life Sciences, Nanjing Normal University, Nanjing, 210000, Jiangsu, China.
Bang-De XiangDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China. xiangbangde@163.com.
Le-Qun LiDepartment of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University, No. 71 Hedi Road, Nanning, 530021, Guangxi, China. li_lequn@263.net.
Ministry of Education of the People's Republic of China · CNTumor Hospital of Guangxi Medical University · CNGuangxi Medical University · CNNanjing Normal University · CN

Funding

Guangxi Nature Sciences Grants 2018GXNSFAA050124Guangxi Nature Sciences Grants 2018GXNSFAA138028Guangxi Nature Sciences Grants Gui Ke AB16380242National Nature Science Foundation of China NSFC 81502533National Nature Science Foundation of China NSFC 81860502National Nature Science Foundation of China NSFC 81960450National Nature Science Foundation of China NSFC 81972306
6 · The paper itself

Abstract

backgroundPortal vein tumor thrombus (PVTT) and microvascular invasion (MVI) are types of intrahepatic vascular metastasis of hepatocellular carcinoma (HCC) and are highly correlated with poor prognosis. However, the underlying biomarkers of PVTT and MVI are unclear.

methodsWe identified a PVTT/MVI-associated gene S100P by cDNA microarray analysis, and assess the potential value of serum S100P measurement in the differential diagnosis of HCC and prediction of MVI status with large retrospective and perspective cohort studies.

resultsThe mRNA and protein of S100P was increased in HCCs with PVTT or MVI. High S100P immunostaining in tumors was correlated with inferior tumor-free survival. Serum S100P values discriminated patients with HCCs from those with benign liver tumors, and it showed predictive potential of MVI status in both retrospective and perspective cohorts. S100P may regulate HCC tumorigenicity and invasive ability; S100P also was associated with up-regulation of CD44, which may mediate HCC cell adhesion to form PVTT/MVI.

conclusionsSerum S100P may be a novel differential diagnostic marker for HCC and a potential predictor of MVI status pre-surgery for HCC patients. S100P overexpression in HCC is highly correlated with the formation of PVTT and MVI, which may make S100P as a potential therapeutic target for HCC metastasis.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsThrombosisBiomarkersCalcium-Binding ProteinsHumansNeoplasm InvasivenessNeoplasm ProteinsPortal VeinPrognosisRetrospective StudiesBiomarkersCalcium-Binding ProteinsNeoplasm ProteinsS100P protein, humanAFPBenign liver tumorBiomarkerCD44Cell invasionCell migrationDiagnosisEarly stagePrognosisSkeleton rearrangementTumor-free survivalTumorigenicity

Identifiers

PMID33495903
OpenAlexW3121771324

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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.