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冬凌草甲素,一种源自东方草药的苦味二萜,通过直接结合ANT2和PHB2抑制胸苷酸合成酶的表达。

Rabdosianone I, a Bitter Diterpene from an Oriental Herb, Suppresses Thymidylate Synthase Expression by Directly Binding to ANT2 and PHB2.

作者信息

Watanabe Motoki, Yamada Yasumasa, Kurumida Yoichi, Kameda Tomoshi, Sukeno Mamiko, Iizuka-Ohashi Mahiro, Sowa Yoshihiro, Iizumi Yosuke, Takakura Hideki, Miyamoto Shingo, Sakai Toshiyuki, Mutoh Michihiro

机构信息

Department of Molecular-Targeting Prevention, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.

Department of Food Science and Human Nutrition, Baika Women's University, Osaka 567-8578, Japan.

出版信息

Cancers (Basel). 2021 Feb 26;13(5):982. doi: 10.3390/cancers13050982.

Abstract

Natural products have numerous bioactivities and are expected to be a resource for potent drugs. However, their direct targets in cells often remain unclear. We found that rabdosianone I, which is a bitter diterpene from an oriental herb for longevity, Hara, markedly inhibited the growth of human colorectal cancer cells by downregulating the expression of thymidylate synthase (TS). Next, using rabdosianone I-immobilized nano-magnetic beads, we identified two mitochondrial inner membrane proteins, adenine nucleotide translocase 2 (ANT2) and prohibitin 2 (PHB2), as direct targets of rabdosianone I. Consistent with the action of rabdosianone I, the depletion of ANT2 or PHB2 reduced TS expression in a different manner. The knockdown of ANT2 or PHB2 promoted proteasomal degradation of TS protein, whereas that of not ANT2 but PHB2 reduced TS mRNA levels. Thus, our study reveals the ANT2- and PHB2-mediated pleiotropic regulation of TS expression and demonstrates the possibility of rabdosianone I as a lead compound of TS suppressor.

摘要

天然产物具有多种生物活性,有望成为强效药物的来源。然而,它们在细胞中的直接靶点往往仍不明确。我们发现,来自一种东方长寿草药夏枯草的苦味二萜——冬凌草甲素,通过下调胸苷酸合成酶(TS)的表达,显著抑制人结肠癌细胞的生长。接下来,我们使用固定有冬凌草甲素的纳米磁珠,鉴定出两种线粒体内膜蛋白,腺嘌呤核苷酸转位酶2(ANT2)和抑制素2(PHB2),作为冬凌草甲素的直接靶点。与冬凌草甲素的作用一致,ANT2或PHB2的缺失以不同方式降低了TS的表达。ANT2或PHB2的敲低促进了TS蛋白的蛋白酶体降解,而不是ANT2而是PHB2的敲低降低了TS mRNA水平。因此,我们的研究揭示了ANT2和PHB2介导的TS表达的多效性调节,并证明了冬凌草甲素作为TS抑制剂先导化合物的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30f3/7956614/8ed33448d7aa/cancers-13-00982-g001a.jpg

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