Fructose-bisphosphate aldolase A (ALDOA) is a key enzyme in glycolysis and is responsible for catalyzing the reversible conversion of fructose-1,6-bisphosphate to glyceraldehydes-3-phosphate and dihydroxyacetone phosphate. ALDOA contributes to various cellular functions such as muscle maintenance, regulation of cell shape and mobility, striated muscle contraction, actin filament organization and ATP biosynthetic process. Here, we reported that ALDOA is a highly expressed in lung squamous cell carcinoma (LSCC) and its expression level is correlated with LSCC metastasis, grades, differentiation status and poor prognosis. Depletion of ALDOA expression in the lung squamous carcinoma NCI-H520 cells reduces the capabilities of cell motility and t...
Loss of hepatic fructose-1, 6-bisphosphate aldolase B (Aldob) leads to a paradoxical up-regulation o...
Although numerous therapeutic strategies have attempted to target aerobic glycolysis to inhibit tumo...
Cancer cells alter their metabolism to support their malignant properties. In this study, we report ...
Human fructose-bisphosphate aldolase A (ALDOA) is a key enzyme in glycolysis that catalyzes the conv...
Background. Glycolysis machinery regulates cancer cell behavior. However, the roles of these glycoly...
Abstract Background Our previous study demonstrated that aldolase A (ALDOA) is overexpressed in clin...
AbstractMuscle fructose 1,6-bisphosphate aldolase (ALDA) is a glycolytic enzyme which may localize b...
Abstract Background ALDOA is a glycolytic enzyme found mainly in developing embryos, adult muscle an...
Glucose metabolism and DNA repair are fundamental cellular processes frequently dysregulated in canc...
D ow nloaded from Colon cancer is the third most common cause of cancer and is the second leading ca...
Introduction: Metabolic reprogramming, known as the Warburg effect, is one of the universal differen...
Reprogramming of cellular energy metabolism is widely accepted to be one of the main hallmarks of ca...
International audienceCancer cells enhance their glycolysis, producing lactate, even in the presence...
Cancer metastasis to distant organs is initiated by tumor cells that disseminate from primary hetero...
<p>(<b>A</b>) Tissue microarray (TMA) analysis of ALDOA expression in 75 pairs of matched LSCCs and ...
Loss of hepatic fructose-1, 6-bisphosphate aldolase B (Aldob) leads to a paradoxical up-regulation o...
Although numerous therapeutic strategies have attempted to target aerobic glycolysis to inhibit tumo...
Cancer cells alter their metabolism to support their malignant properties. In this study, we report ...
Human fructose-bisphosphate aldolase A (ALDOA) is a key enzyme in glycolysis that catalyzes the conv...
Background. Glycolysis machinery regulates cancer cell behavior. However, the roles of these glycoly...
Abstract Background Our previous study demonstrated that aldolase A (ALDOA) is overexpressed in clin...
AbstractMuscle fructose 1,6-bisphosphate aldolase (ALDA) is a glycolytic enzyme which may localize b...
Abstract Background ALDOA is a glycolytic enzyme found mainly in developing embryos, adult muscle an...
Glucose metabolism and DNA repair are fundamental cellular processes frequently dysregulated in canc...
D ow nloaded from Colon cancer is the third most common cause of cancer and is the second leading ca...
Introduction: Metabolic reprogramming, known as the Warburg effect, is one of the universal differen...
Reprogramming of cellular energy metabolism is widely accepted to be one of the main hallmarks of ca...
International audienceCancer cells enhance their glycolysis, producing lactate, even in the presence...
Cancer metastasis to distant organs is initiated by tumor cells that disseminate from primary hetero...
<p>(<b>A</b>) Tissue microarray (TMA) analysis of ALDOA expression in 75 pairs of matched LSCCs and ...
Loss of hepatic fructose-1, 6-bisphosphate aldolase B (Aldob) leads to a paradoxical up-regulation o...
Although numerous therapeutic strategies have attempted to target aerobic glycolysis to inhibit tumo...
Cancer cells alter their metabolism to support their malignant properties. In this study, we report ...