Integrative Evaluation of the Clinical Significance Underlying Protein Arginine Methyltransferases in Hepatocellular Carcinoma

Author:

Jiang Yikun1,Wei Shibo2ORCID,Koo Jin-Mo3,Kim Hea-Ju3,Park Wonyoung3,Zhang Yan4,Guo He5,Ha Ki-Tae3ORCID,Oh Chang-Myung6,Kang Jong-Sun4,Jeong Jee-Heon2,Ryu Dongryeol6ORCID,Kim Kyeong-Jin78,Jo Yunju6ORCID

Affiliation:

1. Department of Orthopedics, The Second Hospital of Jilin University, Changchun 130041, China

2. Department of Precision Medicine, Sungkyunkwan University (SKKU) School of Medicine, Suwon 16419, Republic of Korea

3. Department of Korean Medical Science, School of Korean Medicine, Pusan National University, Yangsan 50612, Republic of Korea

4. Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon 16419, Republic of Korea

5. Department of Obstetrics and Gynecology, The Second Hospital of Jilin University, Changchun 130041, China

6. Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea

7. Department of Biomedical Sciences, College of Medicine, Inha University, Incheon 22212, Republic of Korea

8. Research Center for Controlling Intercellular Communication (RCIC), College of Medicine, Inha University, Incheon 22212, Republic of Korea

Abstract

HCC is a major contributor to cancer-related mortality worldwide. Curative treatments are available for a minority of patients diagnosed at early stages; however, only a few multikinase inhibitors are available and are marginally effective in advanced cases, highlighting the need for novel therapeutic targets. One potential target is the protein arginine methyltransferase, which catalyzes various forms of arginine methylation and is often overexpressed in various cancers. However, the diverse expression patterns and clinical values of PRMTs in HCC remain unclear. In the present study, we evaluated the transcriptional expression of PRMTs in HCC cohorts using publicly available datasets. Our results revealed a significant association between PRMTs and prognosis in HCC patients with diverse clinical characteristics and backgrounds. This highlights the promising potential of PRMTs as prognostic biomarkers in patients with HCC. In particular, single-cell RNA (scRNA) sequencing analysis coupled with another human cohort study highlighted the pivotal role of PRMT1 in HCC progression, particularly in the context of Tex. Translating these findings into specific therapeutic decisions may address the unmet therapeutic needs of patients with HCC.

Funder

National Research Foundation of Korea

Inha University Research Grant

GIST

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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