Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34885
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    CNU IR > Offices > 456 >  Item 310902800/34885
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34885


    Title: The reduced expression of trimethylation of histone H3 at lysine 27 in primary cutaneous mucinous carcinoma
    Authors: Li, Shu-Hao
    Chiou, Chien-Chun
    Chen, Chien-Chin
    Contributors: Chang Gung Mem Hosp Linkou Branch, Dept Dermatol
    Ditmanson Med Fdn Chia Yi Christian Hosp, Dept Dermatol
    Ditmanson Med Fdn Chia Yi Christian Hosp, Dept Pathol
    Chia Nan Univ Pharm & Sci, Dept Cosmet Sci
    Natl Chung Hsing Univ, Rong Hsing Res Ctr Translat Med, PhD Program Translat Med
    Natl Cheng Kung Univ, Coll Biosci & Biotechnol, Dept Biotechnol & Bioind Sci
    Keywords: Dermatology
    epigenetic
    histone
    mucinous carcinoma
    skin
    trimethylation of histone h3 at lysine 27
    Date: 2023
    Issue Date: 2024-12-25 11:05:05 (UTC+8)
    Publisher: WOLTERS KLUWER MEDKNOW PUBLICATIONS
    Abstract: Primary cutaneous mucinous carcinoma (PCMC) is rare, and its carcinogenesis is unclear. Trimethylation of histone H3 at lysine 27 (H3K27me3) is a key regulator in chromatin remodeling-controlled transcription. Focusing on the epigenetic mechanism, we aimed to investigate the expression of H3K27me3 in PCMC by immunohistochemistry. A retrospective cohort of PCMC patients from a tertiary hospital in Taiwan was enrolled to evaluate the clinicopathologic features, treatment outcome, and protein expression. Immunohistochemistry for H3K27me3 was performed on all PCMCs and a comparison group of colonic mucinous adenocarcinoma and pure mucinous carcinoma of the breast. The percentage of H3K27me3-negative tumor cells was calculated and analyzed. Three patients with PCMC were recruited. All PCMCs were solitary and slow growing, arising from the head-and-neck region. All PCMCs had tumor excision without local recurrence or metastasis. The loss of H3K27me3 expression was significant in PCMCs (mean & PLUSMN; standard deviation [SD]: 21.0% & PLUSMN; 6.6%) compared to other mucinous carcinomas (mean & PLUSMN; SD: 3.8% & PLUSMN; 1.7%) (P = 0.019). In conclusion, we report a reduction in H3K27me3 expression in PCMC. In contrast, H3K27me3 expression is retained or mildly reduced in other mucinous carcinomas. This is the first study to indicate a possible role of epigenetic events in the pathobiology of PCMC.
    Relation: Dermatologica Sinica, v.41, n.2, pp.116-120
    Appears in Collections:[Offices] 456

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