Evidence map›Paper›PMID 35332731›Full record

ArticleSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition2022

[PreS1 Antigen of HBV Down-Regulates MHC-Ⅰ on the Surface of Hepatocytes and Promotes Hepatocarcinogenesis].

Jing-Jing Rao, Feng Zeng, Man-Shan Ji, Xiang Xu, Chun-Fang Yu, Jing Yang, Long Liu, Zhi-Xin Liu

Open access · greenAbstract read
In one paragraph

Article in Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition, 2022. 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
0.2field-weighted citation impact, top 53% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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 at 1 institution in 1 country.

Jing-Jing RaoDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Feng ZengDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Man-Shan JiDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Xiang XuDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Chun-Fang YuDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Jing YangDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Long LiuDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Zhi-Xin LiuDepartment of Medical Microbiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Hubei University of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To explore the internal mechanism of hepatocellular carcinoma (HCC) induced by chronic hepatitis B virus (HBV) infection. Methods: L02, HepG2 and Huh7 cells stably overexpressing HBV preS1 antigen were analyzed by flow cytometry, qRT-PCR and tumorigenesis in nude mice to evaluate the effect of preS1 antigen in HBV-related hepatocarcinogenesis. Results: Our results showed that the expression of cancer stem cell (CSCs) related factors and cell surface markers in preS1 overexpressing cells were up-regulated, and the tumorigenicity of these cells was enhanced in nude mice. In addition, preS1 overexpression could down-regulate the expression of major histocompatibility complex Ⅰ (MHC-Ⅰ). The expression of MHC-Ⅰ on the cell surface could be restored by adding interferon gamma (IFN-γ) in the process of cell culturing and the tumorigenicity of cells in nude mice could thus be reduced. Conclusion: Based on the above results, we believe that preS1 is a carcinogen of HBV and that it promotes the formation of liver cancer through down regulating MHC-Ⅰ on the surface of hepatocytes.

Indexed as

Carcinoma, HepatocellularGenes, MHC Class IHepatitis B, ChronicHepatitis B Surface AntigensLiver NeoplasmsProtein PrecursorsAnimalsCarcinogenesisHepatitis B virusHepatocytesMiceMice, NudeHepatitis B Surface Antigenspresurface protein 1, hepatitis B surface antigenProtein PrecursorsHepatitis B virusHepatocellular carcinomaHistocompatibility complex Ⅰ (MHC-Ⅰ)Interferon gamma (IFN-γ)preS1 antigen of HBV

Identifiers

PMID35332731
PMCPMC10409352
OpenAlexW4220658697

What OpenQuestion holds

Textmetadata
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.