Literature DB >> 28359244

Potential Therapeutic Targets in Energy Metabolism Pathways of Breast Cancer.

Rowshan Ara Islam1, Sazzad Hossain2, Ezharul Hoque Chowdhury3.   

Abstract

BACKGROUND: Mutations in proto-oncogenes and tumor suppressor genes make cancer cells proliferate indefinitely. As they possess almost all mechanisms for cell proliferation and survival like healthy cells, it is difficult to specifically target cancer cells in the body. Current treatments in most of the cases are harmful to healthy cells as well. Thus, it would be of great prudence to target specific characters of cancer cells. Since cancer cells avidly use glucose and glutamine to survive and proliferate by upregulating the relevant enzymes and their specific isoforms having important regulatory roles, it has been of great interest recently to target the energy-related metabolic pathways as part of the therapeutic interventions.
OBJECTIVE: This paper summarizes the isozymes overexpressed in breast cancer, their roles of energy metabolism and cross-talks with other important signaling pathways in regulating proliferation, invasion and metastasis in breast cancer.
METHOD: Information has been collected from recently published literature available on Google Scholar and PubMed. Where available, in vivo results were given more importance over in vitro works. RESULT: Like many other cancers, breast cancer shows increased dependence on glycolysis rather than mitochondrial respiration, the main energy source in healthy cells. Cancer cells alter the cellular energy system in a way that helps minimize level of reactive oxygen species and simultaneously produce enough macromolecules- proteins, lipids and nucleotides for cellular proliferation. The altered system enables the cells to grow, proliferate, metastasize and to develop drug resistance. Certain isozymes of metabolic enzymes are overexpressed in breast cancer and the degree of expression of these enzymes vary among subtypes.
CONCLUSION: A clear understanding of the variations of energy metabolism in different molecular subtypes of breast cancer would help in treating each type with a very customized, safer and efficient treatment regimen. Anti-cancer drugs or RNAi or combination of both targeting cancer cell specific isozymes of metabolic enzymes mentioned in this article could offer a great treatment modality for breast cancer. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Breast cancer; TCA cycle; glutaminolysis; glycolysis; pentose phosphate pathway; proto-oncogenes

Mesh:

Substances:

Year:  2017        PMID: 28359244     DOI: 10.2174/1568009617666170330150458

Source DB:  PubMed          Journal:  Curr Cancer Drug Targets        ISSN: 1568-0096            Impact factor:   3.428


  5 in total

Review 1.  Metabolism and immunity in breast cancer.

Authors:  Deyu Zhang; Xiaojie Xu; Qinong Ye
Journal:  Front Med       Date:  2020-10-19       Impact factor: 4.592

2.  A Novel Anti-Hepatitis C Virus and Antiproliferative Agent Alters Metabolic Networks in HepG2 and Hep3B Cells.

Authors:  Adrian Keogh; Sevil Şenkardeş; Jeffrey R Idle; Ş Güniz Küçükgüzel; Diren Beyoğlu
Journal:  Metabolites       Date:  2017-06-02

3.  Distinct pattern of one-carbon metabolism, a nutrient-sensitive pathway, in invasive breast cancer: A metabolomic study.

Authors:  Jéssica Reis Santos; Dan Linetzky Waitzberg; Ismael Dale Cotrim Guerreiro da Silva; Tharcisio Citrangulo Tortelli Junior; Luciana Rodrigues Carvalho Barros; Gisele André Baptista Canuto; Andréa Tedesco Faccio; Lydia Fumiko Yamaguchi; Massuo Jorge Kato; Marina Franco Maggi Tavares; Ana Cristina Martinez; Ângela Flavia Logullo; Raquel Suzana M M Torrinhas; Graziela Ravacci
Journal:  Oncotarget       Date:  2020-05-05

4.  Inborn-like errors of metabolism are determinants of breast cancer risk, clinical response and survival: a study of human biochemical individuality.

Authors:  Ismael da Silva; Rene da Costa Vieira; Carolina Stella; Edson Loturco; André Lopes Carvalho; Carlos Veo; Cristovam Neto; Sandra M Silva; Paulo D'Amora; Marcia Salzgeber; Delcio Matos; Celso R Silva; Jose R Oliveira; Iara Rabelo; Patricia Yamakawa; Rui Maciel; Rosa Biscolla; Maria Chiamolera; Renato Fraietta; Felipe Reis; Marcelo Mori; Dirce Marchioni; Antonio Carioca; Gustavo Maciel; Renato Tomioka; Edmund Baracat; Clovis Silva; Celso Granato; Ricardo Diaz; Bruno Scarpellini; Daniel Egle; Heidi Fiegl; Irmgard Himmel; Christina Troi; Robert Nagourney
Journal:  Oncotarget       Date:  2018-08-03

Review 5.  The Roles of p53 in Mitochondrial Dynamics and Cancer Metabolism: The Pendulum between Survival and Death in Breast Cancer?

Authors:  David E Moulder; Diana Hatoum; Enoch Tay; Yiguang Lin; Eileen M McGowan
Journal:  Cancers (Basel)       Date:  2018-06-08       Impact factor: 6.639

  5 in total

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