학술논문

3-polyunsaturated fatty acids induce cell death through apoptosis and autophagy in glioblastoma cells: In vitro and in vivo
Document Type
Report
Source
Oncology Reports. January, 2018, Vol. 39 Issue 1, p239, 8 p.
Subject
Omega 3 fatty acids -- Health aspects
Glioblastomas -- Development and progression -- Care and treatment
Language
English
ISSN
1021-335X
Abstract
Among brain tumors, glioblastoma (GBM) is the most aggressive type and is associated with the lowest patient survival rate. Numerous lines of evidence have established that omega-3-polyunsaturated fatty acids ([omega]3-PUFAS) have potential for the prevention and therapy of several types of cancers. Docosahexaenoic acid (DHA), an [omega]3-PUFA, was reported to inhibit growth and induce apoptotic and autophagic cell death in several cancer cell lines; however, its effects on GBM cells are still unknown. In the present study, we examined the cytotoxic effect of DHA on the GBM cell lines, D54MG, U87MG, U251MG and GL261. Treatment of GBM cells with DHA induced PARP cleavage, increased the population of sub-G1 cells, and increased the number of TUNEL-positive cells, which are all indicative of apoptosis. Furthermore, treatment of GBM cells with DHA resulted in a significant increase in autophagic activity, as revealed by increased LC3-II levels, GFP-LC3 puncta, and autophagic flux activation, accompanied by activation of 5'-AMP-activated protein kinase (AMPK) and decreases in phosphorylated Akt (p-Akt[Ser.sup.473]) levels and mTOR activity. In vivo, endogenous expression of Caenorhabditis elegans [omega]3-desaturase, which converts [omega]6-PUFAS to [omega]3-PUFAS, in fat-1 transgenic mice yielded a significant decrease in tumor volume following subcutaneous injection of mouse glioma cells (GL261), when compared with wild-type mice. TUNEL-positive cell numbers and LC3-II levels were elevated in tumor tissue from the fat-1 transgenic mice compared with tumor tissue from the wild-type mice. In addition, p-Akt levels were decreased and p-AMPK levels were increased in tumor tissue from the fat-1 transgenic mice. These results indicate that [omega]3-PUFAs induce cell death through apoptosis and autophagy in GBM cells; thus, it may be possible to use [omega]3-PUFAs as chemopreventive and therapeutic agents for GBM. Key words: autophagy, DHA, glioblastoma, omega-3 fatty acid, mTOR
Introduction Glioblastoma (GBM) is the most aggressive and deadliest brain malignancy in adults. According to the latest statistics from the United States National Cancer Institute, it is estimated that 23,000 [...]