Kim Bo Ram, Jeong Yoon A, Na Yoo Jin, Park Seong Hye, Jo Min Jee, Kim Jung Lim, Jeong Soyeon, Lee Suk-Young, Kim Hong Jun, Oh Sang Cheul, Lee Dae-Hee
Department of Oncology, Korea University Guro Hospital, Seoul, Republic of Korea.
Graduate School of Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
Oncotarget. 2017 Oct 16;8(60):101952-101964. doi: 10.18632/oncotarget.21882. eCollection 2017 Nov 24.
Genipin, a major component of Ellis fruit, has been shown to inhibit the growth of gastric, prostate, and breast cancers. However, the anti-proliferative activity of genipin in colorectal cancer (CRC) has not been characterized. Herein, we demonstrated that genipin inhibits the proliferation of CRC cells and that genipin suppressed the Hedgehog pathway. Further investigation showed that p53 and NOXA protein levels were increased during inhibition of Hedgehog pathway-mediated apoptosis in CRC cells. We also showed that p53 modulated the expression of NOXA during genipin-induced apoptosis, and suppression via SMO also played a role in this process. Subsequently, GLI1 was ubiquitinated by the E3 ligase PCAF. In a xenograft tumor model, genipin suppressed tumor growth, which was also associated with Hedgehog inactivation. Taken together, these results suggest that genipin induces apoptosis through the Hedgehog signaling pathway by suppressing p53. These findings reveal a novel regulatory mechanism involving Hedgehog/p53/NOXA signaling in the modulation of CRC cell apoptosis and tumor-forming defects.
京尼平是栀子果实的主要成分,已被证明可抑制胃癌、前列腺癌和乳腺癌的生长。然而,京尼平在结直肠癌(CRC)中的抗增殖活性尚未得到表征。在此,我们证明京尼平抑制CRC细胞的增殖,并且京尼平抑制了Hedgehog信号通路。进一步研究表明,在CRC细胞中抑制Hedgehog信号通路介导的凋亡过程中,p53和NOXA蛋白水平升高。我们还表明,在京尼平诱导的凋亡过程中,p53调节NOXA的表达,并且通过SMO的抑制在该过程中也发挥了作用。随后,GLI1被E3连接酶PCAF泛素化。在异种移植肿瘤模型中,京尼平抑制肿瘤生长,这也与Hedgehog失活有关。综上所述,这些结果表明京尼平通过抑制p53,经由Hedgehog信号通路诱导凋亡。这些发现揭示了一种涉及Hedgehog/p53/NOXA信号传导的新型调节机制,该机制参与CRC细胞凋亡和肿瘤形成缺陷的调节。