Open Access
Therapeutic benefit of combining calorie-restricted ketogenic diet and glutamine targeting in late-stage experimental glioblastoma
Purna Mukherjee
1
,
Zachary M Augur
1
,
Mingyi Li
1
,
Collin Hill
2
,
Bennett Greenwood
2
,
Marek A Domin
3
,
Gramoz Kondakci
2
,
Niven R Narain
2
,
Michael A. Kiebish
2
,
Roderick T. Bronson
4
,
Gabriel Arismendi Morillo
5
,
Christos Chinopoulos
6
,
Thomas N. Seyfried
1
2
BERG LLC, Framingham, USA
|
Publication type: Journal Article
Publication date: 2019-05-29
scimago Q1
wos Q1
SJR: 2.071
CiteScore: 8.8
Impact factor: 5.1
ISSN: 23993642
PubMed ID:
31149644
General Biochemistry, Genetics and Molecular Biology
Medicine (miscellaneous)
General Agricultural and Biological Sciences
Abstract
Glioblastoma (GBM) is an aggressive primary human brain tumour that has resisted effective therapy for decades. Although glucose and glutamine are the major fuels that drive GBM growth and invasion, few studies have targeted these fuels for therapeutic management. The glutamine antagonist, 6-diazo-5-oxo-L-norleucine (DON), was administered together with a calorically restricted ketogenic diet (KD-R) to treat late-stage orthotopic growth in two syngeneic GBM mouse models: VM-M3 and CT-2A. DON targets glutaminolysis, while the KD-R reduces glucose and, simultaneously, elevates neuroprotective and non-fermentable ketone bodies. The diet/drug therapeutic strategy killed tumour cells while reversing disease symptoms, and improving overall mouse survival. The therapeutic strategy also reduces edema, hemorrhage, and inflammation. Moreover, the KD-R diet facilitated DON delivery to the brain and allowed a lower dosage to achieve therapeutic effect. The findings support the importance of glucose and glutamine in driving GBM growth and provide a therapeutic strategy for non-toxic metabolic management. Purna Mukherjee et al demonstrate that administering a glutamine analogue together with a calorie-restricted ketogenic diet can reduce brain tumour growth and inflammation, while enhancing survival, in two syngeneic orthotopic mouse models.
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115
Total citations:
115
Citations from 2024:
43
(37.39%)
Cite this
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RIS |
BibTex
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GOST
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Mukherjee P. et al. Therapeutic benefit of combining calorie-restricted ketogenic diet and glutamine targeting in late-stage experimental glioblastoma // Communications Biology. 2019. Vol. 2. No. 1. 200
GOST all authors (up to 50)
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Mukherjee P., Augur Z. M., Li M., Hill C., Greenwood B., Domin M. A., Kondakci G., Narain N. R., Kiebish M. A., Bronson R. T., Arismendi Morillo G., Chinopoulos C., Seyfried T. N. Therapeutic benefit of combining calorie-restricted ketogenic diet and glutamine targeting in late-stage experimental glioblastoma // Communications Biology. 2019. Vol. 2. No. 1. 200
Cite this
RIS
Copy
TY - JOUR
DO - 10.1038/s42003-019-0455-x
UR - https://doi.org/10.1038/s42003-019-0455-x
TI - Therapeutic benefit of combining calorie-restricted ketogenic diet and glutamine targeting in late-stage experimental glioblastoma
T2 - Communications Biology
AU - Mukherjee, Purna
AU - Augur, Zachary M
AU - Li, Mingyi
AU - Hill, Collin
AU - Greenwood, Bennett
AU - Domin, Marek A
AU - Kondakci, Gramoz
AU - Narain, Niven R
AU - Kiebish, Michael A.
AU - Bronson, Roderick T.
AU - Arismendi Morillo, Gabriel
AU - Chinopoulos, Christos
AU - Seyfried, Thomas N.
PY - 2019
DA - 2019/05/29
PB - Springer Nature
IS - 1
VL - 2
PMID - 31149644
SN - 2399-3642
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2019_Mukherjee,
author = {Purna Mukherjee and Zachary M Augur and Mingyi Li and Collin Hill and Bennett Greenwood and Marek A Domin and Gramoz Kondakci and Niven R Narain and Michael A. Kiebish and Roderick T. Bronson and Gabriel Arismendi Morillo and Christos Chinopoulos and Thomas N. Seyfried},
title = {Therapeutic benefit of combining calorie-restricted ketogenic diet and glutamine targeting in late-stage experimental glioblastoma},
journal = {Communications Biology},
year = {2019},
volume = {2},
publisher = {Springer Nature},
month = {may},
url = {https://doi.org/10.1038/s42003-019-0455-x},
number = {1},
pages = {200},
doi = {10.1038/s42003-019-0455-x}
}