| Literature DB >> 33420169 |
Masahiro Maeyama1, Kazuhiro Tanaka2, Masamitsu Nishihara3, Yasuhiro Irino4, Masakazu Shinohara5,6, Hiroaki Nagashima7, Hirotomo Tanaka1, Satoshi Nakamizo1, Mitsuru Hashiguchi1, Yuichi Fujita1, Masaaki Kohta1, Eiji Kohmura1, Takashi Sasayama1.
Abstract
The ketogenic diet (KD) is a high fat and low carbohydrate diet that produces ketone bodies through imitation of starvation. The combination of KD and Bevacizumab (Bev), a VEGF inhibitor, is considered to further reduce the supply of glucose to the tumor. The metabolite changes in U87 glioblastoma mouse models treated with KD and/or Bev were examined using gas chromatography-mass spectrometry. The combination therapy of KD and Bev showed a decrease in the rate of tumor growth and an increase in the survival time of mice, although KD alone did not have survival benefit. In the metabolome analysis, the pattern of changes for most amino acids are similar between tumor and brain tissues, however, some amino acids such as aspartic acid and glutamic acid were different between tumors and brain tissues. The KD enhanced the anti-tumor efficacy of Bev in a glioblastoma intracranial implantation mouse model, based on lowest levels of microvascular density (CD31) and cellular proliferation markers (Ki-67 and CCND1) in KD + Bev tumors compared to the other groups. These results suggested that KD combined with Bev may be a useful treatment strategy for patients with GBM.Entities:
Year: 2021 PMID: 33420169 PMCID: PMC7794443 DOI: 10.1038/s41598-020-79465-x
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379