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7α,15-Dihydroxydehydroabietic acid from Pinus koraiensis inhibits the promotion of angiogenesis through downregulation of VEGF, p-Akt and p-ERK in HUVECs.

作者信息

Lee Tae Kyoung, Park Jun Yeon, Yu Jae Sik, Jang Tae Su, Oh Seong Taek, Pang Changhyun, Ko Yoon-Joo, Kang Ki Sung, Kim Ki Hyun

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.

College of Korean Medicine, Gachon University, Seongnam 461-701, Republic of Korea.

出版信息

Bioorg Med Chem Lett. 2018 Apr 1;28(6):1084-1089. doi: 10.1016/j.bmcl.2018.02.014. Epub 2018 Feb 9.

DOI:10.1016/j.bmcl.2018.02.014
PMID:29459209
Abstract

Pinus koraiensis pinecones are considered an undesired waste by-product of the processing of seeds. However, recent studies of the potential anti-tumor effects of the pinecones have led to increasing interest in their chemical constituents. The present study examined the potential antiangiogenic effects of the constituents of pinecones and further characterized their underlying mechanisms of action. Chemical investigation of a water extract of P. koraiensis pinecones led to the isolation and identification of the eight main components including five diterpenoids (1-5), two monoterpenes (6,7) and a phenolic acid (8). The structure of the compounds was determined by spectroscopic analysis of NMR spectra and LC/MS analysis. Of the isolated compounds, 7α,15-dihydroxydehydroabietic acid (5) significantly inhibited the promotion of angiogenesis in human umbilical vein endothelial cells (HUVECs). Compound 5 inhibited angiogenesis through downregulation of the VEGF, p-Akt and p-ERK signaling pathways. These results provide experimental evidence of a novel biological activity of 7α,15-dihydroxydehydroabietic acid (5) as a potential antiangiogenic substance. This study also suggests that compound 5 could potentially be a useful adjuvant therapeutic substance for cancer prevention and treatment.

摘要

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