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Cited 2 time in webofscience Cited 1 time in scopus
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Correlation with Apoptosis Process through RNA-Seq Data Analysis of Hep3B Hepatocellular Carcinoma Cells Treated with <i>Glehnia littoralis</i> Extract (GLE)open access

Authors
Park, Min-YeongLee, SujinKim, Hun-HwanJeong, Se-HyoAbusaliya, AbuyaseerBhosale, Pritam BhangwanSeong, Je-KyungPark, Kwang-IlHeo, Jeong-DooAhn, MeejungKim, Hyun-WookKim, Gon-Sup
Issue Date
Sep-2024
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
RNA-sequencing; apoptotic process; Hep3B; liver cancer
Citation
International Journal of Molecular Sciences, v.25, no.17
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
25
Number
17
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/74045
DOI
10.3390/ijms25179462
ISSN
1661-6596
1422-0067
Abstract
Glehnia littoralis is a perennial herb found in coastal sand dunes throughout East Asia. This herb has been reported to have hepatoprotective, immunomodulatory, antioxidant, antibacterial, antifungal, anti-inflammatory, and anticancer activities. It may be effective against hepatocellular carcinoma (HCC). However, whether this has been proven through gene-level RNA-seq analysis is still being determined. Therefore, we are attempting to identify target genes for the cell death process by analyzing the transcriptome of Hep3B cells among HCC treated with GLE (Glehnia littoralis extract) using RNA-seq. Hep3B was used for the GLE treatment, and the MTT test was performed. Hep3B was then treated with GLE at a set concentration of 300 mu g/mL and stored for 24 h, followed by RNA isolation and sequencing. We then used the data to create a plot. As a result of the MTT analysis, cell death was observed when Hep3B cells were treated with GLE, and the IC50 was about 300 mu g/mL. As a result of making plots using the RNA-seq data of Hep3B treated with 300 mu g/mL GLE, a tendency for the apoptotic process was found. Flow cytometry and annexin V/propidium iodide (PI) staining verified the apoptosis of HEP3B cells treated with GLE. Therefore, an increase or decrease in the DEGs involved in the apoptosis process was confirmed. The top five genes increased were GADD45B, DDIT3, GADD45G, CHAC1, and PPP1R15A. The bottom five genes decreased were SGK1, CX3CL1, ZC3H12A, IER3, and HNF1A. In summary, we investigated the RNA-seq dataset of GLE to identify potential targets that may be involved in the apoptotic process in HCC. These goals may aid in the identification and management of HCC.
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