Diarylheptanoids suppress proliferation of pancreatic cancer PANC-1 cells through modulating shh-Gli-FoxM1 pathway

Pancreatic cancer is one of the leading causes of cancer, and it has the lowest 5-year survival rates. It is necessary to develop more potent anti-pancreatic cancer drugs to overcome the fast metastasis and resistance to surgery, radiotherapy, chemotherapy, and combinations of these. We have identif...

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Published inArchives of pharmacal research Vol. 40; no. 4; pp. 509 - 517
Main Authors Dong, Guang-zhi, Jeong, Ji Hye, Lee, Yu-ih, Lee, So Yoon, Zhao, Hui-Yuan, Jeon, Raok, Lee, Hwa Jin, Ryu, Jae-Ha
Format Journal Article
LanguageEnglish
Published Seoul Pharmaceutical Society of Korea 01.04.2017
대한약학회
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ISSN0253-6269
1976-3786
DOI10.1007/s12272-017-0905-2

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Summary:Pancreatic cancer is one of the leading causes of cancer, and it has the lowest 5-year survival rates. It is necessary to develop more potent anti-pancreatic cancer drugs to overcome the fast metastasis and resistance to surgery, radiotherapy, chemotherapy, and combinations of these. We have identified several diarylheptanoids as anti-pancreatic cancer agents from Alpinia officinarum (lesser galangal) and Alnus japonica . These diarylheptanoids suppressed cell proliferation and induced the cell cycle arrest of pancreatic cancer cells (PANC-1). Among them, the most potent compounds 1 and 7 inhibited the shh-Gli-FoxM1 pathway and their target gene expression in PANC-1 cells. Furthermore, they suppressed the expression of the cell cycle associated genes that were rescued by the overexpression of exogenous FoxM1. Taken together, (E)-7-(4-hydroxy-3-methoxyphenyl)-1-phenylhept-4-en-3-one ( 1 ) from Alpinia officinarum (lesser galangal) and platyphyllenone ( 7 ) from Alnus japonica inhibit PANC-1 cell proliferation by suppressing the shh-Gli-FoxM1 pathway, and they can be potential candidates for anti-pancreatic cancer drug development.
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G704-000010.2017.40.4.010
ISSN:0253-6269
1976-3786
DOI:10.1007/s12272-017-0905-2