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Genipin suppresses colorectal cancer cells by inhibiting the Sonic Hedgehog pathway

Authors
Kim, Bo RamJeong, Yoon A.Na, Yoo JinPark, Seong HyeJo, Min JeeKim, Jung LimJeong, SoyeonLee, Suk-YoungKim, Hong JunOh, Sang CheulLee, Dae-Hee
Issue Date
24-11월-2017
Publisher
IMPACT JOURNALS LLC
Keywords
genipin; Hedgehog pathway; NOXA; GLI1; ubiquitin
Citation
ONCOTARGET, v.8, no.60, pp.101952 - 101964
Indexed
SCIE
SCOPUS
Journal Title
ONCOTARGET
Volume
8
Number
60
Start Page
101952
End Page
101964
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81512
DOI
10.18632/oncotarget.21882
ISSN
1949-2553
Abstract
Genipin, a major component of Gardenia jasminoides 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.
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