國家衛生研究院 NHRI:Item 3990099045/12154
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    NHRI > NHRI Graduate Student Program > Others > Periodical Articles >  Item 3990099045/12154


    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/12154


    Title: CYP17A1 maintains the survival of glioblastomas by regulating SAR1-Mediated endoplasmic reticulum health and redox homeostasis
    Authors: Lin, HY;Ko, CY;Kao, TJ;Yang, WB;Tsai, YT;Chuang, JY;Hu, SL;Yang, PY;Lo, WL;Hsu, TI
    Contributors: NHRI Graduate Student Program
    Abstract: Cytochrome P450 (CYP) 17A1 is an important steroidogenic enzyme harboring 17alpha-hydroxylase and performing 17,20 lyase activities in multiple steps of steroid hormone synthesis, including dehydroepiandrosterone (DHEA) biosynthesis. Previously, we showed that CYP17A1-mediated DHEA production clearly protects glioblastomas from temozolomide-induced apoptosis, leading to drug resistance. Herein, we attempt to clarify whether the inhibition of CYP17A1 has a tumor-suppressive effect, and to determine the steroidogenesis-independent functions of CYP17A1 in glioblastomas. Abiraterone, an inhibitor of CYP17A1, significantly inhibits the proliferation of A172, T98G, and PT#3 (the primary glioblastoma cells) by inducing apoptosis. In parallel, abiraterone potently suppresses tumor growth in mouse models through transplantation of PT#3 cells to the back or to the brain. Based on evidence that abiraterone induces endoplasmic reticulum (ER) stress, followed by the accumulation of reactive oxygen species (ROS), CYP17A1 is important for ER health and redox homeostasis. To confirm our hypothesis, we showed that CYP17A1 overexpression prevents the initiation of ER stress and attenuates ROS production by regulating SAR1a/b expression. Abiraterone dissociates SAR1a/b from ER-localized CYP17A1, and induces SAR1a/b ubiquitination, leading to degradation. Furthermore, SAR1 overexpression rescues abiraterone-induced apoptosis and impairs redox homeostasis. In addition to steroid hormone synthesis, CYP17A1 associates with SAR1a/b to regulate protein processing and maintain ER health in glioblastomas.
    Date: 2019-09-16
    Relation: Cancers. 2019 Sep 16;11(9):Article number 1378.
    Link to: http://dx.doi.org/10.3390/cancers11091378
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=2072-6694&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000489719000163
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85074374582
    Appears in Collections:[Others] Periodical Articles

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