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Mitochondrial dysfunction in cancer

Mitochondrion, 2004
Nearly a century of scientific research has revealed a number of notable differences in the structure and function of mitochondria between normal and cancer cells, including differences in metabolic activity, molecular composition, and mtDNA sequence.
Josephine S, Modica-Napolitano   +1 more
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Mitochondrial dysfunction and age

Current Opinion in Clinical Nutrition and Metabolic Care, 2007
Mitochondrial dysfunction is commonly thought to result from oxidative damage that leads to defects in the electron transport chain (ETC). In this review, we highlight new research indicating that there are early changes in mitochondrial function that precede ETC defects and are reversible thereby providing the possibility of slowing the tempo of ...
Kevin E, Conley   +2 more
openaire   +2 more sources

Mitochondrial Dysfunction and Glaucoma

Journal of Glaucoma, 2009
Glaucoma is increasingly recognized as a neurodegenerative disorder, characterized by the accelerated loss of retinal ganglion cells (RGCs) and their axons. Open angle glaucoma prevalence and incidence increase exponentially with increasing age, yet the pathophysiology underlying increasing age as a risk factor for glaucoma is not well understood ...
George Y X, Kong   +3 more
openaire   +2 more sources

Mitochondrial dysfunction and mitochondrial dynamics-The cancer connection

open access: yesBiochimica Et Biophysica Acta - Bioenergetics, 2017
Mitochondrial dysfunction is a hallmark of many diseases. The retrograde signaling initiated by dysfunctional mitochondria can bring about global changes in gene expression that alters cell morphology and function. Typically, this is attributed to disruption of important mitochondrial functions, such as ATP production, integration of metabolism ...
Narayan G Avadhani   +2 more
exaly   +3 more sources

Mitochondrial Dysfunction in Gliomas

Seminars in Pediatric Neurology, 2013
Mitochondrial (mt) dysfunction in gliomas has been linked to abnormalities of mt energy metabolism, marked by a metabolic shift from oxidative phosphorylation to glycolysis ("Warburg effect"), disturbances in mt membrane potential regulation and apoptotic signaling, as well as to somatic mutations involving the Krebs cycle enzyme isocitrate ...
Christos D, Katsetos   +2 more
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Mitochondrial Dysfunction in Autism

Seminars in Pediatric Neurology, 2013
Using data of the current prevalence of autism as 200:10,000 and a 1:2000 incidence of definite mitochondrial (mt) disease, if there was no linkage of autism spectrum disorder (ASD) and mt disease, it would be expected that 1 in 110 subjects with mt disease would have ASD and 1 in 2000 individuals with ASD would have mt disease.
Agustín, Legido   +2 more
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Mitochondrial dysfunction in osteoarthritis

Mitochondrion, 2004
In osteoarthritis (OA) a time or age dependent process leads to aberrant cartilage structure which is characterized by reduced number of chondrocytes, loss of existing cartilage extracellular matrix, the production of matrix with abnormal composition and pathologic matrix calcification.
Francisco J, Blanco   +2 more
openaire   +2 more sources

Mitochondrial Dysfunction in Epilepsy

Seminars in Pediatric Neurology, 2013
Epilepsy is the most common neurologic disorder worldwide and is characterized by recurrent unprovoked seizures. The mitochondrial (mt) respiratory chain is the final common pathway for cellular energy production through the process of oxidative phosphorylation.
Divya S, Khurana   +3 more
openaire   +2 more sources

Mitochondrial Dysfunction in Hepatitis C

Journal of Clinical Gastroenterology, 2005
Chronic hepatitis C induces a state of hepatic oxidative stress that is more pronounced than that present in many other inflammatory liver diseases. This review summarizes recent information that the hepatitis C virus (HCV) core protein plays an important role in this phenomenon.
Masaaki, Korenaga   +5 more
openaire   +2 more sources

Mitochondrial dysfunction in bipolar disorder

2010
Phosphorus magnetic resonance spectroscopic studies in bipolar disorder revealed altered brain energy metabolism resembling that of chronic progressive external ophthalmoplegia (CPEO). Mood disorder is one characteristic symptom in several families of CPEO caused by mutations of three genes, ANT1, Twinkle, and POLG.
openaire   +3 more sources

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