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J Pharmacol Sci ; 146(4): 249-258, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34049792

ABSTRACT

Momordin Ic (MI) is a natural pentacyclic triterpenoid enriched in various Chinese natural medicines such as the fruit of Kochia scoparia (L.) Schrad. Studies have shown that MI presents antitumor properties in liver and prostate cancers. However, the activity and potential mechanisms of MI against colorectal cancer remain elusive. Here, we showed that MI inhibited cell proliferation with G0/1 phase cell cycle arrest in colon cancer cells. Moreover, it was observed that MI increased apoptosis compared to untreated cells. Further investigation showed that the SUMOylation of c-Myc was enhanced by MI and led to the down-regulated protein level of c-Myc, which is involved in regulating cell proliferation and apoptosis. SENP1 has been demonstrated to be critical for the SUMOylation of c-Myc. Meanwhile, knockdown of SENP1 by siRNA abolished the effects of MI on c-Myc level and cell viability in colon cancer cells. Together, these results revealed that MI exerted an anti-tumor activity in colon cancer cells via SENP1/c-Myc signaling pathway. These finding provide an insight into the potential of MI for colon cancer therapy.


Subject(s)
Apoptosis/drug effects , Apoptosis/genetics , Colonic Neoplasms/genetics , Colonic Neoplasms/pathology , Cysteine Endopeptidases/metabolism , G1 Phase Cell Cycle Checkpoints/drug effects , G1 Phase Cell Cycle Checkpoints/genetics , Oleanolic Acid/analogs & derivatives , Proto-Oncogene Proteins c-myc/metabolism , Resting Phase, Cell Cycle/drug effects , Signal Transduction/genetics , Signal Transduction/physiology , Antineoplastic Agents, Phytogenic , Bassia scoparia/chemistry , Cell Line, Tumor , Cell Proliferation/drug effects , Cell Proliferation/genetics , Colonic Neoplasms/drug therapy , Humans , Oleanolic Acid/isolation & purification , Oleanolic Acid/pharmacology , Oleanolic Acid/therapeutic use , Phytotherapy
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