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1.
J Cell Biol ; 220(7)2021 07 05.
Artigo em Inglês | MEDLINE | ID: mdl-33988680

RESUMO

LC3s are canonical proteins necessary for the formation of autophagosomes. We have previously established that two paralogs, LC3B and LC3C, have opposite activities in renal cancer, with LC3B playing an oncogenic role and LC3C a tumor-suppressing role. LC3C is an evolutionary late gene present only in higher primates and humans. Its most distinct feature is a C-terminal 20-amino acid peptide cleaved in the process of glycine 126 lipidation. Here, we investigated mechanisms of LC3C-selective autophagy. LC3C autophagy requires noncanonical upstream regulatory complexes that include ULK3, UVRAG, RUBCN, PIK3C2A, and a member of ESCRT, TSG101. We established that postdivision midbody rings (PDMBs) implicated in cancer stem-cell regulation are direct targets of LC3C autophagy. LC3C C-terminal peptide is necessary and sufficient to mediate LC3C-dependent selective degradation of PDMBs. This work establishes a new noncanonical human-specific selective autophagic program relevant to cancer stem cells.


Assuntos
Autofagossomos/genética , Autofagia/genética , Proteínas Associadas aos Microtúbulos/genética , Proteínas Relacionadas à Autofagia/genética , Proteínas de Ligação a DNA , Complexos Endossomais de Distribuição Requeridos para Transporte/genética , Células HeLa , Humanos , Peptídeos/genética , Fosfatidilinositol 3-Quinases/genética , Proteínas Serina-Treonina Quinases/genética , Proteólise , Fatores de Transcrição , Proteínas Supressoras de Tumor/genética
2.
J Clin Invest ; 131(1)2021 01 04.
Artigo em Inglês | MEDLINE | ID: mdl-32970633

RESUMO

BACKGROUNDClear cell renal cell carcinoma (ccRCC) is the most common histologically defined renal cancer. However, it is not a uniform disease and includes several genetic subtypes with different prognoses. ccRCC is also characterized by distinctive metabolic reprogramming. Tobacco smoking (TS) is an established risk factor for ccRCC, with unknown effects on tumor pathobiology.METHODSWe investigated the landscape of ccRCCs and paired normal kidney tissues using integrated transcriptomic, metabolomic, and metallomic approaches in a cohort of white males who were long-term current smokers (LTS) or were never smokers (NS).RESULTSAll 3 Omics domains consistently identified a distinct metabolic subtype of ccRCCs in LTS, characterized by activation of oxidative phosphorylation (OXPHOS) coupled with reprogramming of the malate-aspartate shuttle and metabolism of aspartate, glutamate, glutamine, and histidine. Cadmium, copper, and inorganic arsenic accumulated in LTS tumors, showing redistribution among intracellular pools, including relocation of copper into the cytochrome c oxidase complex. A gene expression signature based on the LTS metabolic subtype provided prognostic stratification of The Cancer Genome Atlas ccRCC tumors that was independent of genomic alterations.CONCLUSIONThe work identified the TS-related metabolic subtype of ccRCC with vulnerabilities that can be exploited for precision medicine approaches targeting metabolic pathways. The results provided rationale for the development of metabolic biomarkers with diagnostic and prognostic applications using evaluation of OXPHOS status. The metallomic analysis revealed the role of disrupted metal homeostasis in ccRCC, highlighting the importance of studying effects of metals from e-cigarettes and environmental exposures.FUNDINGDepartment of Defense, Veteran Administration, NIH, ACS, and University of Cincinnati Cancer Institute.


Assuntos
Carcinoma de Células Renais/metabolismo , Reprogramação Celular , Neoplasias Renais/metabolismo , Fumar Tabaco/efeitos adversos , Fumar Tabaco/metabolismo , Carcinoma de Células Renais/patologia , Feminino , Humanos , Neoplasias Renais/patologia , Masculino , Fumar Tabaco/patologia
3.
J Phys Ther Sci ; 28(3): 1016-9, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27134404

RESUMO

[Purpose] The purpose of this study was to describe the relationship between three practical measures used to characterize muscle mass: mid-arm circumference, maximum calf circumference, and muscle mass index determined using bioimpedance analysis. [Subjects and Methods] Thirty-eight ambulatory women residing in a senior center (mean age, 83 years) participated in this cross-sectional study. Their mid-arm circumference and maximum calf circumference were measured bilaterally and they all underwent bioimpedance analysis. Relationships were examined by using Pearson (r) correlations, Cronbach's alpha, and factor analysis. [Results] Circumferential measures correlated significantly with one another (r = 0.745-0.968) and with the muscle mass index determined with bioimpedance analysis (r = 0.480-0.628). The Cronbach's alpha for the measures was 0.905. Factor analysis confirmed that all of the measures were reflective of a common construct. [Conclusion] On the basis of their correlations with one another and the muscle mass index determined with bioimpedance analysis, circumferential measures of the mid-arm or calf may be considered crude indicators of reduced muscle mass.

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