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  1. Article ; Online: Multiomics profiling of buffy coat and plasma unveils etiology-specific signatures in hepatocellular carcinoma.

    Hong, Jiwon / Eun, Jung Woo / Baek, Geum Ok / Cheong, Jae Youn / Park, Seryoung / Kim, Soon Sun / Cho, Hyo Jung / Lim, Su Bin

    Clinical and molecular hepatology

    2024  

    Abstract: Background/aims: Hepatocellular carcinoma (HCC) is a leading cause of cancer mortality worldwide. Despite identification of several biomarkers for HCC diagnosis, challenges such as low sensitivity and intratumoral heterogeneity have impeded early ... ...

    Abstract Background/aims: Hepatocellular carcinoma (HCC) is a leading cause of cancer mortality worldwide. Despite identification of several biomarkers for HCC diagnosis, challenges such as low sensitivity and intratumoral heterogeneity have impeded early detection, highlighting the need for etiology-specific blood biomarkers.
    Methods: We generated whole-transcriptome sequencing (WTS) and targeted proteome data from buffy coat and plasma samples from HCC patients. By integrating etiological information on viral infection, we investigated the etiology-specific gene expression landscape at the blood level. Validation of differentially expressed genes (DEGs) was performed using publicly available RNA-seq datasets and qRT‒PCR with AUC analyses.
    Results: Differential expression analyses with multiomics data revealed distinct gene expression profiles between HBV-associated HCC and nonviral HCC, indicating the presence of etiology-specific blood biomarkers. The identified DEGs were validated across multiple independent datasets, underscoring their utility as biomarkers. Additionally, single-cell RNA-seq analysis of HCC confirmed differences in DEG expression across distinct immune cell types.
    Conclusions: Our buffy coat WTS data and plasma proteome data may serve as reliable sources for identifying etiology-specific blood biomarkers of HCC and might contribute to discovery of therapeutic targets for HCC across different etiologies.
    Language English
    Publishing date 2024-03-15
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2672560-5
    ISSN 2287-285X ; 2287-2728
    ISSN (online) 2287-285X
    ISSN 2287-2728
    DOI 10.3350/cmh.2024.0042
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Corrigendum to: Deoxypodophyllotoxin Induces ROSMediated Apoptosis by Modulating the PI3K/AKT and p38 MAPK-Dependent Signaling in Oral Squamous Cell Carcinoma.

    Seo, Ji-Hye / Yoon, Goo / Park, Seryoung / Shim, Jung-Hyun / Chae, Jung-Il / Jeon, Young-Joo

    Journal of microbiology and biotechnology

    2022  Volume 32, Issue 10, Page(s) 1355

    Language English
    Publishing date 2022-10-28
    Publishing country Korea (South)
    Document type Published Erratum
    ZDB-ID 2412195-2
    ISSN 1738-8872 ; 1738-8872
    ISSN (online) 1738-8872
    ISSN 1738-8872
    DOI 10.4014/jmb.2022.3210.1355
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Deoxypodophyllotoxin Induces ROS-Mediated Apoptosis by Modulating the PI3K/AKT and p38 MAPK-Dependent Signaling in Oral Squamous Cell Carcinoma.

    Seo, Ji-Hye / Yoon, Goo / Park, Seryoung / Shim, Jung-Hyun / Chae, Jung-Il / Jeon, Young-Joo

    Journal of microbiology and biotechnology

    2022  Volume 32, Issue 9, Page(s) 1103–1109

    Abstract: Deoxypodophyllotoxin (DPT), a naturally occurring flavonolignan, possesses several pharmacological properties, including anticancer property. However, the mechanisms underlying DPT mode of action in oral squamous cell carcinoma (OSCC) remain unknown. ... ...

    Abstract Deoxypodophyllotoxin (DPT), a naturally occurring flavonolignan, possesses several pharmacological properties, including anticancer property. However, the mechanisms underlying DPT mode of action in oral squamous cell carcinoma (OSCC) remain unknown. This study aimed to investigate the anticancer effects of DPT on OSCC and the underlying mechanisms. Results of the MTT assay revealed that DPT significantly reduced the cell viability in a time- and dose-dependent manner. Flow cytometry analysis revealed that DPT induces apoptosis in OSCC cells in a dose-dependent manner. Moreover, DPT enhanced the production of mitochondrial reactive oxygen species (ROS) in OSCC cells. Mechanistically, DPT induced apoptosis in OSCC cells by suppressing the PI3K/AKT signaling pathway while activating the p38 MAPK signaling to regulate the expression of apoptotic proteins. Treatment with SC79, an AKT activator, reversed the effects of DPT on AKT signaling in OSCC cells. Taken together, these results provide the basis for the use of DPT in combination with conventional chemotherapy for the treatment of oral cancer.
    MeSH term(s) Apoptosis ; Carcinoma, Squamous Cell/drug therapy ; Carcinoma, Squamous Cell/metabolism ; Carcinoma, Squamous Cell/pathology ; Cell Line, Tumor ; Cell Proliferation ; Drugs, Chinese Herbal ; Flavonolignans/pharmacology ; Flavonolignans/therapeutic use ; Head and Neck Neoplasms ; Humans ; Mouth Neoplasms/drug therapy ; Mouth Neoplasms/pathology ; Phosphatidylinositol 3-Kinases/metabolism ; Podophyllotoxin/analogs & derivatives ; Proto-Oncogene Proteins c-akt/metabolism ; Reactive Oxygen Species/metabolism ; Squamous Cell Carcinoma of Head and Neck ; p38 Mitogen-Activated Protein Kinases/metabolism
    Chemical Substances Drugs, Chinese Herbal ; Flavonolignans ; Reactive Oxygen Species ; deoxypodophyllotoxin (69222-20-4) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; p38 Mitogen-Activated Protein Kinases (EC 2.7.11.24) ; Podophyllotoxin (L36H50F353)
    Language English
    Publishing date 2022-08-24
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2412195-2
    ISSN 1738-8872 ; 1738-8872
    ISSN (online) 1738-8872
    ISSN 1738-8872
    DOI 10.4014/jmb.2207.07012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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