Evidence map›Paper›PMID 35765957›Full record

ArticleBosnian journal of basic medical sciences2022

ORM 1 as a biomarker of increased vascular invasion and decreased sorafenib sensitivity in hepatocellular carcinoma.

Jiangning Gu, Shiqi Xu, Xiang Chen, Haifeng Luo, Guang Tan, Wenjing Qi, Feng Ling, Chenqi Wang, Feiliyan Maimaiti, Yunlong Chen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Bosnian journal of basic medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  4. Bile acid regulation of xenobiotic nuclear receptors on the expressions of orosomucoids in the liver.American journal of physiology. Endocrinology and metabolism · 2025
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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

13 authors at 1 institution in 1 country.

Jiangning GuDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Shiqi XuDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Xiang ChenDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Haifeng LuoDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Guang TanDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Wenjing QiDepartment of Pathology, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Feng LingDepartment of Nursing, The First affiliated Hospital of Dalian Medical University, Dalian, China.
Chenqi WangDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Feiliyan MaimaitiDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Yunlong ChenDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Lili YangDepartment of Hepatobiliary Surgery, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Menghong YinDepartment of Sports Medicine, Dalian Municipal Central Hospital, Dalian Medical University, Dalian, Liaoning Province, China.
Dan ChenDepartment of Pathology, the First affiliated hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to clarify the role of Orosomucoid 1 (ORM1) in the development and therapy resistance in hepatocellular carcinoma (HCC). The mRNA expression level of ORM1 was analyzed via integrative analysis of Gene Express Omnibus (GEO) and The Cancer Genome Atlas (TCGA) datasets. The protein expression level of ORM1 in our cohort was determined using immunohistochemistry. Correlation analysis was used to investigate the relationship between ORM1 expression and clinical parameters. The Cell Counting Kit-8 assay was used to clarify the role of ORM1 in HCC malignant behaviors, including cell growth and sorafenib sensitivity, in vitro. The results indicated that ORM1 was significantly downregulated in the hepatic cancer cells compared to that in the non-cancerous cells. However, it was upregulated in microvascular invasion samples, especially in the cancer embolus compared to that in the surrounding tumor cells. Though Kaplan-Meier analysis did not show an association of ORM1 expression with the overall survival rates of HCC patients, univariate analysis indicated that ORM1 expression was highly correlated with tumor grade and stage. An in vitro assay also revealed that downregulation of ORM1 led to the suppression of tumor growth and enhancement of sorafenib sensitivity without epithelial-to-mesenchymal transition (EMT) alteration, which was consistent with our bioinformatic analysis. Hence, ORM1 played a key role in HCC tumorigenesis and may serve as a potential target for the development of therapeutics against HCC in the future.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsBiomarkersGene Expression Regulation, NeoplasticHumansOrosomucoidRNA, MessengerSorafenibBiomarkersORM1 protein, humanOrosomucoidRNA, MessengerSorafenib

Identifiers

PMID35765957
PMCPMC9589312
OpenAlexW4283735659

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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.