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Flavokawain B Inhibits Growth of Cholangiocarcinoma Cells by Suppressing the Akt Pathway.
Son, Jun Hyuk; Choi, Young Hoon; Lee, Sang Hyub; Paik, Woo Hyun; Ryu, Ji Kon; Kim, Yong-Tae.
Affiliation
  • Son JH; Department of Internal Medicine, Inje University Ilsan Paik Hospital, Goyang, Republic of Korea.
  • Choi YH; Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Lee SH; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea gidoctor@snu.ac.kr.
  • Paik WH; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Ryu JK; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Kim YT; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
In Vivo ; 37(3): 1077-1084, 2023.
Article in En | MEDLINE | ID: mdl-37103099
ABSTRACT
BACKGROUND/

AIM:

Cholangiocarcinoma is a devastating malignancy with limited treatment options and poor prognosis. Natural products have gained considerable attention for showing antitumor effects with less toxicities. Flavokawain B (FKB), a natural product, has been studied for its antitumor effects on various cancer cells. However, the anti-tumor effect of FKB on cholangiocarcinoma cells remains unknown. This study aimed at investigating the antitumor effect of FKB on cholangiocarcinoma cells in vitro and in vivo. MATERIALS AND

METHODS:

SNU-478, a human cholangiocarcinoma cell line, was used in this study. Effects of FKB on cell growth inhibition and apoptosis were investigated. The synergistic anti-tumor effect of FKB and cisplatin in combination was also evaluated. Western blotting was performed to examine the underlying molecular mechanisms of the effect of FKB. A xenograft mouse model study was performed to investigate the effect of FKB in vivo.

RESULTS:

FKB inhibited cell proliferation of cholangiocarcinoma cells in a concentration- and time-dependent manner. FKB also induced cellular apoptosis additively in combination with cisplatin. Akt pathway was suppressed by FKB either alone or in combination with cisplatin. In the xenograft model, FKB treatment in combination with cisplatin/gemcitabine significantly inhibited tumor growth of SNU-478 cells.

CONCLUSION:

FKB showed an antitumor effect through the induction of apoptosis, which was mediated by suppressing the Akt pathway in cholangiocarcinoma cells. However, the synergistic effect of FKB and cisplatin was not definite.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cholangiocarcinoma / Proto-Oncogene Proteins c-akt Limits: Animals / Humans Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cholangiocarcinoma / Proto-Oncogene Proteins c-akt Limits: Animals / Humans Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2023 Document type: Article