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1.
Journal of Medical Postgraduates ; (12): 537-542, 2020.
Artigo em Chinês | WPRIM | ID: wpr-821888

RESUMO

Mitochondria, which play an important role in cell metabolism, stress response and cell death, are the key organelles that regulate the energy balance of cells. Under the influence of internal and external environment, damaged or senescent mitochondria pose a serious threat to cell survival. Mitophagy refers to the selective elimination of dysfunctional mitochondria to maintain the homeostasis of the intracellular environment. FUN14 domain containing 1 (FUNDC1) is a newly discovered mitophagy receptor protein, which plays an important regulatory role in mediating mitophagy. This paper mainly reviews the recent research progress of FUNDC1 regulation mechanism and its pathophysiological significance in mitophagy.

2.
Journal of Southern Medical University ; (12): 47-49, 2009.
Artigo em Chinês | WPRIM | ID: wpr-339069

RESUMO

<p><b>OBJECTIVE</b>To study the expression of Aurora-B in human glioma tissue and its significance.</p><p><b>METHODS</b>The total RNA was extracted from 41 human glioma tissues and 11 normal brain tissues by Trizol reagent. After reverse transcription of the total RNA into cDNAs, Aurora-B mRNA expressions in these samples were detected by quantitative real-time PCR. The protein expression in these samples was detected using immunohistochemical staining.</p><p><b>RESULTS</b>Aurora-B mRNA and protein expressions were significantly increased in glioma tissues as compared with those in normal brain tissues.</p><p><b>CONCLUSION</b>Aurora-B mRNA and protein show markedly higher expressions in glioma tissue, suggesting that Aurora-B may be one of the malignant biomarkers in the pathogenesis and progression of human glioma.</p>


Assuntos
Feminino , Humanos , Masculino , Aurora Quinase B , Aurora Quinases , Biomarcadores Tumorais , Metabolismo , Neoplasias Encefálicas , Patologia , Glioma , Metabolismo , Patologia , Proteínas Serina-Treonina Quinases , Genética , Metabolismo , RNA Mensageiro , Genética , Metabolismo , Células Tumorais Cultivadas
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