Literature DB >> 28179305

The Anticancer Effects of Novel α-Bisabolol Derivatives Against Pancreatic Cancer.

Yoshihiko Murata1, Toshio Kokuryo2, Yukihiro Yokoyama1, Junpei Yamaguchi1, Tomohiro Miwa1, Masatoshi Shibuya3, Yoshihiko Yamamoto3, Masato Nagino1.   

Abstract

Pancreatic cancer is highly malignant, characterized by aggressive proliferation, invasion, and metastasis. α-Bisabolol is an oily sesquiterpene alcohol derived from a variety of plants. We previously demonstrated that α-bisabolol is a potential therapeutic agent for pancreatic cancer. The aim of this study was to develop α-bisabolol derivatives which are more potent than the parent compound and may be clinically useful against pancreatic cancer. First, 22 derivatives of α-bisabolol were designed and synthesized. α-Bisabolol derivatives 4 and 5 had more potent inhibitory effects on the proliferation of pancreatic cancer cells than did α-bisabolol. Next, 15 additional α-bisabolol derivatives were designed and synthesized based on the structure of α-bisabolol derivatives 4 and 5 Among them, α-bisabolol derivative 5 had the strongest inhibitory effect on proliferation. This novel compound reduced the proliferation of various pancreatic cancer cell lines, such as KLM1, Panc1, and KP4. In addition, the compound induced higher levels of apoptosis in pancreatic cancer cell lines than did α-bisabolol. α-Bisabolol derivative 5 inhibited xenograft tumor growth and reduced dissemination of pancreatic cancer to peritoneal nodules. The compound strongly suppressed AKT expression in the peritoneal nodules. Reduced AKT expression in peritoneal nodules is consistent with an anticancer effect. These data indicate that α-bisabolol derivative 5 effectively prevents the progression of pancreatic cancer via inhibition of AKT. Taken together, the results showed that this compound has attractive therapeutic properties as a novel anticancer drug for pancreatic cancer. Copyright
© 2017, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Entities:  

Keywords:  AKT; apoptosis; pancreas cancer; peritoneal dissemination; α-Bisabolol derivatives

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Year:  2017        PMID: 28179305     DOI: 10.21873/anticanres.11352

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  4 in total

Review 1.  Structural and Chemical Biology of Terpenoid Cyclases.

Authors:  David W Christianson
Journal:  Chem Rev       Date:  2017-08-25       Impact factor: 60.622

2.  (-)-α-Bisabolol Alleviates Atopic Dermatitis by Inhibiting MAPK and NF-κB Signaling in Mast Cell.

Authors:  Guangxia Li; Huayan Wu; Liqin Sun; Kang Cheng; Zhi Lv; Kaixian Chen; Fei Qian; Yiming Li
Journal:  Molecules       Date:  2022-06-21       Impact factor: 4.927

Review 3.  Health Benefits, Pharmacological Effects, Molecular Mechanisms, and Therapeutic Potential of α-Bisabolol.

Authors:  Lujain Bader Eddin; Niraj Kumar Jha; Sameer N Goyal; Yogeeta O Agrawal; Sandeep B Subramanya; Salim M A Bastaki; Shreesh Ojha
Journal:  Nutrients       Date:  2022-03-25       Impact factor: 5.717

4.  In Vitro Scolicidal Activity of the Sesquiterpenes Isofuranodiene, α-Bisabolol and Farnesol on Echinococcus granulosus Protoscoleces.

Authors:  Mohammad Reza Youssefi; Ali Nikpay; Niloufar Hassanpour; Aida Mirzapour; Parisa Saleh Tabari; Roman Pavela; Filippo Maggi; Riccardo Petrelli
Journal:  Molecules       Date:  2020-08-07       Impact factor: 4.411

  4 in total

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