Detailed Information on Publication Record
2016
Impaired mitophagy in Fanconi anemia is dependent on mitochondrial fission
SHYAMSUNDER, Pavithra, Milan EŠNER, Maunish BARVALIA, Yu Jun WU, Tomáš LOJA et. al.Basic information
Original name
Impaired mitophagy in Fanconi anemia is dependent on mitochondrial fission
Authors
SHYAMSUNDER, Pavithra (702 Singapore), Milan EŠNER (203 Czech Republic, belonging to the institution), Maunish BARVALIA (356 India), Yu Jun WU (702 Singapore), Tomáš LOJA (703 Slovakia, belonging to the institution), Huat Bay BOON (702 Singapore), Matilde E. LLEONART (724 Spain), Rama S VERMA (356 India), Lumír KREJČÍ (203 Czech Republic, guarantor, belonging to the institution) and Alex LYAKHOVICH (643 Russian Federation, belonging to the institution)
Edition
Oncotarget, New York, Impact Journals, 2016, 1949-2553
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
Genetics and molecular biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 5.168
RIV identification code
RIV/00216224:14110/16:00091248
Organization unit
Faculty of Medicine
UT WoS
000387153200048
Keywords in English
mitophagy; impaired autophagy; Fanconi anemia; ROS; oxidative stress
Tags
International impact, Reviewed
Změněno: 9/1/2017 14:30, Ing. Mgr. Věra Pospíšilíková
Abstract
V originále
Fanconi anemia (FA) is a rare genetic disorder associated with bone-marrow failure, genome instability and cancer predisposition. Recently, we and others have demonstrated dysfunctional mitochondria with morphological alterations in FA cells accompanied by high reactive oxygen species (ROS) levels. Mitochondrial morphology is regulated by continuous fusion and fission events and the misbalance between these two is often accompanied by autophagy. Here, we provide evidence of impaired autophagy in FA. We demonstrate that FA cells have increased number of autophagic (presumably mitophagic) events and accumulate dysfunctional mitochondria due to an impaired ability to degrade them. Moreover, mitochondrial fission accompanied by oxidative stress (OS) is a prerequisite condition for mitophagy in FA and blocking this pathway may release autophagic machinery to clear dysfunctional mitochondria.