Anti-Cancer Effect of Lambertianic Acid by Inhibiting the AR in LNCaP Cells

Autor: Sung-Hoon Kim, Eun-Ok Lee, Hyo-Jeong Lee, Seon-Ok Lee, Myoung-Sun Lee
Jazyk: angličtina
Rok vydání: 2016
Předmět:
0301 basic medicine
LNCaP
lambertianic acid
androgen receptor
anticancer
Carboxylic Acids
Apoptosis
Cell Cycle Proteins
lcsh:Chemistry
0302 clinical medicine
Nandrolone
Cyclin D1
RNA
Small Interfering

lcsh:QH301-705.5
Spectroscopy
bcl-2-Associated X Protein
biology
Caspase 3
Chemistry
General Medicine
Caspase 9
Computer Science Applications
Proto-Oncogene Proteins c-bcl-2
Biochemistry
Receptors
Androgen

030220 oncology & carcinogenesis
RNA Interference
medicine.symptom
Down-Regulation
Antineoplastic Agents
Naphthalenes
Article
Catalysis
Inorganic Chemistry
03 medical and health sciences
Bcl-2-associated X protein
Cell Line
Tumor

medicine
Humans
Physical and Theoretical Chemistry
Molecular Biology
Cell Proliferation
Cell growth
Organic Chemistry
Cyclin-Dependent Kinase 4
Cyclin-Dependent Kinase 6
Prostate-Specific Antigen
G1 Phase Cell Cycle Checkpoints
030104 developmental biology
Mechanism of action
lcsh:Biology (General)
lcsh:QD1-999
biology.protein
Cancer research
Cyclin-dependent kinase 6
Tumor Suppressor Protein p53
Zdroj: International Journal of Molecular Sciences, Vol 17, Iss 7, p 1066 (2016)
International Journal of Molecular Sciences; Volume 17; Issue 7; Pages: 1066
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES(17): 7
International Journal of Molecular Sciences
ISSN: 1422-0067
Popis: Lambertianic acid (LA) is known to have anti-allergic and antibacterial effects. However, the anticancer activities and mechanism of action of LA have not been investigated. Therefore, the anticancer effects and mechanism of LA are investigated in this study. LA decreased not only AR protein levels, but also cellular and secretory levels of PSA. Furthermore, LA inhibited nuclear translocation of the AR induced by mibolerone. LA suppressed cell proliferation by inducing G(1) arrest, downregulating CDK4/6 and cyclin D1 and activating p53 and its downstream molecules, p21 and p27. LA induced apoptosis and the expression of related proteins, including cleaved caspase-9 and -3, c-PARP and BAX, and inhibited BCl-2. The role of AR in LA-induced apoptosis was assessed by using siRNA. Collectively, these findings suggest that LA exerts the anticancer effect by inhibiting AR and is a valuable therapeutic agent in prostate cancer treatment.
Databáze: OpenAIRE