多胺
卵巢癌
癌症研究
癌变
癌症
恶性肿瘤
生物
生物化学
遗传学
作者
Yihui Chen,Ricardo A. Léon-Letelier,Ali H. Abdel Sater,Jody Vykoukal,Jennifer B. Dennison,Samir Hanash,Johannes F. Fahrmann
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2023-01-19
卷期号:15 (3): 623-623
被引量:5
标识
DOI:10.3390/cancers15030623
摘要
c-MYC and its paralogues MYCN and MYCL are among the most frequently amplified and/or overexpressed oncoproteins in ovarian cancer. c-MYC plays a key role in promoting ovarian cancer initiation and progression. The polyamine pathway is a bona fide target of c-MYC signaling, and polyamine metabolism is strongly intertwined with ovarian malignancy. Targeting of the polyamine pathway via small molecule inhibitors has garnered considerable attention as a therapeutic strategy for ovarian cancer. Herein, we discuss the involvement of c-MYC signaling and that of its paralogues in promoting ovarian cancer tumorigenesis. We highlight the potential of targeting c-MYC-driven polyamine metabolism for the treatment of ovarian cancers and the utility of polyamine signatures in biofluids for early detection applications.
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