Evidence map›Paper›PMID 33437370›Full record

ArticleAmerican journal of translational research2020

CYP2J2 promotes the development of hepatocellular carcinoma by increasing the EETs production to improve HIF-1α stability.

Liang Gui, Qiang Xu, Juju Huang, Gaojue Wu, Hong Tang, Li Hui, Ping Hua, Lili Zhang, Yingwei Zhu

Abstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Review
  2. Integrated bioinformatics to identify and validate the role of oxidative stress-related gene EPHX2 in laryngeal cancer.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
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.

Liang GuiDepartment of Vascular Surgery, Beijing Hospital, National Center of Gerontology Beijing 100730, China.
Qiang XuDepartment of Intervention, Wujin Hospital Affiliated to Jiangsu University Changzhou 213002, Jiangsu, China.
Juju HuangDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.
Gaojue WuDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.
Hong TangDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.
Li HuiDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.
Ping HuaDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.
Lili ZhangDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.
Yingwei ZhuDepartment of Gastroenterology, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University Wuxi 214002, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to explore the function and mechanism of Cytochrome P450 2J2 (CYP2J2) epoxygenase and epoxyeicosatrienoic acids (EETs) in the malignant development of hepatocellular carcinoma (HCC).

methodThe expressional levels of EETs and CYP2J2 in HCC tissues and cell lines were quantified by ELISA, western blot and RT-qPCR, respectively. The effects of EET and CYP2J2 on HCC development were analyzed by CCK-8 assays, flow cytometry analysis, colony formation and transwell assays. The effect of CYP2J2-EET metabolism on stability of HIF-1α was detected by western blot experiments. HIF-1α inhibitor, YC-1, was used to probe the relationship between HIF-1α and metastasis of HCC cells. Finally, xenograft experiments were established to investigate the function of CYP2J2-EETs metabolism in HCC tumorigenesis

resultCYP2J2, 11, 12-EET and 14, 15-EET were up-regulated in HCC tissues and Huh-7, HepG2 cell lines. Addition of exogenous 14, 15-EET accelerated proliferation and metastasis of HCC cells. Knockdown of CYP2J2 inhibited growth and metastasis of HCC cells and malignant xenograft, which was obviously reversed by addition of 14, 15-EET. Moreover, in Huh-7 and HepG2 cells, CYP2J2-EET metabolism elevated the expression of HIF-1α and its downstream factors including VEGFA, PDK1, GLUT1 and DDIT4 through suppressing the expression of PHD. Treatment of YC-1 remarkably suppressed the HCC cells proliferation and restored the effect of 14, 15-EET on tumor size

conclusionThe up-regulated levels of CYP2J2 and 14, 15-EET in HCC cells improved the stability of HIF-1α thourgh inhibiting PHD expression, which further promoted the malignant development of HCC.

Indexed as

1415-EETCYP2J2Hepatocellular carcinomaHIF-1αPHD

Identifiers

PMID33437370
PMCPMC7791520

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