Evidence map›Paper›PMID 36132142›Full record

ArticleFrontiers in oncology2022

OIT3 serves as a novel biomarker of hepatocellular carcinoma by mediating ferroptosis

Jie Wen, Abudureyimujiang Aili, Yao Xue Yan, YuLin Lai, Shaoqing Niu, Shasha He, Xiaokai Zhang, Guixiong Zhang, Jiaping Li

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Jie WenDepartment of Interventional Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China and Department of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.
Abudureyimujiang AiliDepartment of Medical Oncology and Radiation Sickness, Peking University Third Hospital, Beijing, China.
Yao Xue YanDepartment of Dermatology, Peking University People's Hospital, Beijing, China.
YuLin LaiDeparment of Radiotherapy, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Shaoqing NiuDeparment of Radiotherapy, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Shasha HeDeparment of Radiotherapy, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Xiaokai ZhangDepartment of Interventional Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Guixiong ZhangDepartment of Interventional Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Jiaping LiDepartment of Interventional Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Oncoprotein-Induced Transcript 3 Protein (OIT3) was identified as a liver-specific gene with abnormal expression in hepatocellular carcinoma (HCC). Herein, we aimed to examine the function and specific mechanism of OIT3 in HCC. Methods: Bioinformatic analyses and tissue microarray Results: Low expression of OIT3 was observed in HCC and predicted a poor clinical outcome. Ectopic expression of OIT3 could inhibit the proliferation, migration, and invasion abilities of HCC cells. Mechanistically, OIT3 upregulated the expression of ALOX15 and CYP4F3, thus inducing arachidonic acid increase, ROS accumulation, and lipid peroxidation, and eventually causing ferroptosis. OIT3 was validated as a prognostic predictor for HCC patients. Conclusions: Our findings revealed a novel role of OIT3 in the process of tumorigenesis of HCC. OIT3 inhibited reproliferation, migration, and invasion of HCC cells by triggering ferroptosis, which indicates that OIT3 could serve as a potential biomarker in HCC.

Indexed as

arachidonic acidbiomarkerferroptosisHCCOIT3

Identifiers

PMID36132142
PMCPMC9483180
OpenAlexW4294607192

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.