Detailed Information on Publication Record
2021
Identification of metabolic changes leading to cancer susceptibility in Fanconi anemia cells
ABAD, Etna, Sara SAMINO, Robert L. GRODZICKI, Giovanni PAGANO, Marco TRIFUOGGI et. al.Basic information
Original name
Identification of metabolic changes leading to cancer susceptibility in Fanconi anemia cells
Authors
ABAD, Etna (724 Spain), Sara SAMINO (724 Spain), Robert L. GRODZICKI (840 United States of America), Giovanni PAGANO (380 Italy), Marco TRIFUOGGI (380 Italy), Dmitry GRAIFER (643 Russian Federation), David POTĚŠIL (203 Czech Republic, belonging to the institution), Zbyněk ZDRÁHAL (203 Czech Republic, guarantor, belonging to the institution), Oscar YANES (724 Spain) and Alex LYAKHOVICH (643 Russian Federation)
Edition
Cancer Letters, Elsevier, 2021, 0304-3835
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 9.756
RIV identification code
RIV/00216224:14740/21:00119598
Organization unit
Central European Institute of Technology
UT WoS
000629990700018
Keywords in English
Fanconi anemia; Cancer predisposition; de novo purine biosynthesis; Fumarate; Purinosome; Metabolic reprogramming
Tags
International impact, Reviewed
Změněno: 10/10/2024 14:12, Ing. Martina Blahová
Abstract
V originále
Fanconi anemia (FA) is a chromosomal instability disorder of bone marrow associated with aplastic anemia, congenital abnormalities and a high risk of malignancies. The identification of more than two dozen FA genes has revealed a plethora of interacting proteins that are mainly involved in repair of DNA interstrand crosslinks (ICLs). Other important findings associated with FA are inflammation, oxidative stress response, mitochondrial dysfunction and mitophagy. In this work, we performed quantitative proteomic and metabolomic analyses on defective FA cells and identified a number of metabolic abnormalities associated with cancer. In particular, an increased de novo purine biosynthesis, a high concentration of fumarate, and an accumulation of purinosomal clusters were found. This was in parallel with decreased OXPHOS and altered glycolysis. On the whole, our results indicate an association between the need for nitrogenous bases upon impaired DDR in FA cells with a subsequent increase in purine metabolism and a potential role in oncogenesis.
Links
GBP206/12/G151, research and development project |
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LM2015043, research and development project |
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LQ1601, research and development project |
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90043, large research infrastructures |
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