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Aralin from Aralia elata is a newly identified type II ribosome- inactivating protein, which preferentially induces apoptosis in cancer cells. In this study, we identified that the aralin receptor is a 110-kDa high-density lipoprotein-binding protein (HDLBP), which functions as a HDL receptor. The sensitivities of tumor cell lines to aralin were dependent on the expression levels of the 110-kDa HDLBP and its forced expression in aralin-resistant Huh7 cells conferred aralin sensitivity. HDLBP-knockdown HeLa cells showed a significant aralin resistance in vitro and in vivo. Conversely, ectopic expression of the 150-kDa HDLBP resulted in increased aralin sensitivity in vivo, accompanying enhanced expression of the 110-kDa HDLBP. Thus, these results showed that the 110-kDa HDLBP in lipid rafts acted as an aralin receptor and that its expression levels determined aralin sensitivity, suggesting that aralin could be a promising anticancer drug for HDLBP-overexpressing tumors. Copyright © 2014 Elsevier Inc. All rights reserved.

Citation

Hiroko Otsuka, Yoshitaka Gotoh, Takashi Komeno, Takahide Ono, Yasushi Kawasaki, Naoyuki Iida, Yoshio Shibagaki, Seisuke Hattori, Makoto Tomatsu, Hirotada Akiyama, Fumio Tashiro. Aralin, a type II ribosome-inactivating protein from Aralia elata, exhibits selective anticancer activity through the processed form of a 110-kDa high-density lipoprotein-binding protein: a promising anticancer drug. Biochemical and biophysical research communications. 2014 Oct 10;453(1):117-23

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PMID: 25261720

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