» Articles » PMID: 36902470

Ovarian Cancer and Glutamine Metabolism

Abstract

Cancer cells are known to have a distinct metabolic profile and to exhibit significant changes in a variety of metabolic mechanisms compared to normal cells, particularly glycolysis and glutaminolysis, in order to cover their increased energy requirements. There is mounting evidence that there is a link between glutamine metabolism and the proliferation of cancer cells, demonstrating that glutamine metabolism is a vital mechanism for all cellular processes, including the development of cancer. Detailed knowledge regarding its degree of engagement in numerous biological processes across distinct cancer types is still lacking, despite the fact that such knowledge is necessary for comprehending the differentiating characteristics of many forms of cancer. This review aims to examine data on glutamine metabolism and ovarian cancer and identify possible therapeutic targets for ovarian cancer treatment.

Citing Articles

Branched-chain amino acid catabolism promotes ovarian cancer cell proliferation via phosphorylation of mTOR.

Lusk H, Haughan M, Bergsten T, Burdette J, Sanchez L bioRxiv. 2024; .

PMID: 39464074 PMC: 11507863. DOI: 10.1101/2024.10.15.618560.


Metabolomic Analysis of Histological Composition Variability of High-Grade Serous Ovarian Cancer Using H HR MAS NMR Spectroscopy.

Skorupa A, Klimek M, Ciszek M, Pakulo S, Cichon T, Cichon B Int J Mol Sci. 2024; 25(20).

PMID: 39456684 PMC: 11507550. DOI: 10.3390/ijms252010903.


NEK6 dampens FOXO3 nuclear translocation to stabilize C-MYC and promotes subsequent de novo purine synthesis to support ovarian cancer chemoresistance.

Liu J, Wang H, Wan H, Yang J, Gao L, Wang Z Cell Death Dis. 2024; 15(9):661.

PMID: 39256367 PMC: 11387829. DOI: 10.1038/s41419-024-07045-2.


Molecular mechanisms of cisplatin resistance in ovarian cancer.

Jiang C, Shen C, Ni M, Huang L, Hu H, Dai Q Genes Dis. 2024; 11(6):101063.

PMID: 39224110 PMC: 11367050. DOI: 10.1016/j.gendis.2023.06.032.


Glutamine metabolism prognostic index predicts tumour microenvironment characteristics and therapeutic efficacy in ovarian cancer.

Gao L, Wei Z, Ying F, Huang L, Zhang J, Sun S J Cell Mol Med. 2024; 28(7):e18198.

PMID: 38506093 PMC: 10951877. DOI: 10.1111/jcmm.18198.


References
1.
Hatipoglu A, Menon D, Levy T, Frias M, Foster D . Inhibiting glutamine utilization creates a synthetic lethality for suppression of ATP citrate lyase in KRas-driven cancer cells. PLoS One. 2022; 17(10):e0276579. PMC: 9586366. DOI: 10.1371/journal.pone.0276579. View

2.
Rooth C . Ovarian cancer: risk factors, treatment and management. Br J Nurs. 2013; 22(17):S23-30. DOI: 10.12968/bjon.2013.22.Sup17.S23. View

3.
Willems L, Jacque N, Jacquel A, Neveux N, Trovati Maciel T, Lambert M . Inhibiting glutamine uptake represents an attractive new strategy for treating acute myeloid leukemia. Blood. 2013; 122(20):3521-32. PMC: 3829119. DOI: 10.1182/blood-2013-03-493163. View

4.
Fu Y, Lin H, Liu X, Fang W, Meadows G . Cell death of prostate cancer cells by specific amino acid restriction depends on alterations of glucose metabolism. J Cell Physiol. 2010; 224(2):491-500. DOI: 10.1002/jcp.22148. View

5.
Sung P, Chang Y, Chao K, Chuang C . Global distribution pattern of histological subtypes of epithelial ovarian cancer: a database analysis and systematic review. Gynecol Oncol. 2014; 133(2):147-54. DOI: 10.1016/j.ygyno.2014.02.016. View