PMID- 34249720 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220424 IS - 2234-943X (Print) IS - 2234-943X (Electronic) IS - 2234-943X (Linking) VI - 11 DP - 2021 TI - ASRGL1 Correlates With Immune Cell Infiltration in Hepatocellular Carcinoma and Can Serve as a Prognostic Biomarker. PG - 680070 LID - 10.3389/fonc.2021.680070 [doi] LID - 680070 AB - BACKGROUND: The enzyme L-asparaginase (ASRGL1) catalyzes the hydrolysis of L-asparagine (Asn) to L-aspartic acid (Asp) and ammonia. Numerous studies have shown a strong correlation between ASRGL1 expression and tumorigenesis. However, the expression and biological function of ASRGL1 in hepatocellular carcinoma (HCC) are still unclear. METHODS: We explored the mRNA expression of ASRGL1 in HCC using the HCCDB, Oncomine, and TIMER 2.0 databases. Western blotting and immunohistochemical analyses were also used to determine the mRNA expression of ASRGL1 in HCC. LinkedOmics was used to analyze the genes co-expressed with ASRGL1 and regulators including kinases, miRNAs, and transcription factors. The Gene Ontology (GO) terms and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways of the co-expressed genes were also investigated using LinkedOmics. The correlation between ASRGL1 expression and immune infiltrates was analyzed using the TIMER 2.0 and Gene Expression Profiling Interactive Analysis (GEPIA) databases. The effects of ASRGL1 expression on patient outcome were investigated using the UALCAN and GEPIA databases, and the Kaplan-Meier plotter. c-Bioportal was used to explore the mutations of ASRGL1 in HCC. RESULTS: Compared with the adjacent tissues, ASRGL1 was upregulated in HCC. High ASRGL1 expression in HCC indicated poor relapse-free survival, progression-free survival, disease-specific survival, and overall survival. The expression of ASRGL1 was significantly correlated with infiltrating levels of B cells, CD4+ T cells, macrophages, neutrophils, and dendritic cells in HCC. CONCLUSION: Our findings suggest that ASRGL1 is overexpressed in HCC and that ASRGL1 expression was significantly correlated with immune infiltration in HCC and prognosis. Therefore, ASRGL1 may serve as a biomarker for the early diagnosis and treatment of HCC. CI - Copyright (c) 2021 Xue, Gao, Cui, Zhang, Lei, Li, Zhu and Qin. FAU - Xue, Cailin AU - Xue C AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Gao, Peng AU - Gao P AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Cui, Xiaohan AU - Cui X AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Zhang, Xudong AU - Zhang X AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Lei, Jin AU - Lei J AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Li, Renzhi AU - Li R AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Zhu, Chunfu AU - Zhu C AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. FAU - Qin, Xihu AU - Qin X AD - Department of Hepatobiliary Surgery, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou, China. LA - eng PT - Journal Article DEP - 20210625 PL - Switzerland TA - Front Oncol JT - Frontiers in oncology JID - 101568867 PMC - PMC8267417 OTO - NOTNLM OT - ASRGL1 OT - HCC OT - biomarker OT - immune OT - immune cell infiltration COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2021/07/13 06:00 MHDA- 2021/07/13 06:01 PMCR- 2021/01/01 CRDT- 2021/07/12 05:56 PHST- 2021/03/26 00:00 [received] PHST- 2021/05/31 00:00 [accepted] PHST- 2021/07/12 05:56 [entrez] PHST- 2021/07/13 06:00 [pubmed] PHST- 2021/07/13 06:01 [medline] PHST- 2021/01/01 00:00 [pmc-release] AID - 10.3389/fonc.2021.680070 [doi] PST - epublish SO - Front Oncol. 2021 Jun 25;11:680070. doi: 10.3389/fonc.2021.680070. eCollection 2021.