Physiological indexes, psychological resilience, sensory functions, and sleep quality on the cognitive function of older adults with pre-frailty: a predictive study

Population ageing has increased the prevalence of prefrailty comorbid with cognitive impairment among older adults. However, few studies have explored the risk factors common to both prefrailty and cognitive impairment. This study determined the predictive accuracy of demographic characteristics, physiological indexes, psychological resilience, sensory function, and sleep quality on the cognitive function of older adults with prefrailty. In this cross-sectional study, the physiological indexes, psychological resilience, sensory function, sleep quality, and cognitive function of 167 community-dwelling older adults with prefrailty recruited through purposive sampling were measured. SPSS software was used for data coding and compilation. Data analysis involved the use of descriptive statistics, the independent samples t test, the chi-square test, and logistic regression. Overall, in cognitive function, there was no difference in gender but were in age, were incapable of text messaging, had a greater number of chronic diseases, were less able to perform activities of daily living, had low psychological resilience, and had depressive tendencies. In addition, Text messaging capability and depression status can all predict the cognitive impairment state of prefrail older elderly. Physiological indexes, psychological resilience, sensory function, and sleep quality can affect cognitive function in older adults with prefrailty. Meanwhile, depressive tendencies and the inability to send text messages on a mobile device constituted critical predictors of cognitive function in the participants

Effect of bis(hydroxymethyl) alkanoate curcuminoid derivative MTH-3 on cell cycle arrest, apoptotic and autophagic pathway in triple-negative breast adenocarcinoma MDA-MB-231 cells: An in vitro study

Curcumin has been shown to exert potential antitumor activity in vitro and in vivo involved in multiple signaling pathways. However, the application of curcumin is still limited because of its poor hydrophilicity and low bio-availability. In the present study, we investigated the therapeutic effects of a novel and water soluble bis(hydroxymethyl) alkanoate curcuminoid derivative, MTH-3, on human breast adenocarcinoma MDA-MB-231 cells. This study investigated the effect of MTH-3 on cell viability, cell cycle and induction of autophagy and apoptosis in MDA-MB-231 cells. After 24-h treatment with MTH-3, a concentration-dependent decrease in MDA-MB-231 cell viability was observed, and the IC50 value was 5.37±1.22 μM. MTH-3 significantly triggered G2/M phase arrest and apoptosis in MDA-MB-231 cells. Within a 24-h treatment, MTH-3 decreased the CDK1 activity by decreasing CDK1 and cyclin B1 protein levels. MTH-3-induced apoptosis was further confirmed by morphological assessment and Annexin V/PI staining assay. Induction of apoptosis caused by MTH-3 was accompanied by an apparent increase of DR3, DR5 and FADD and, as well as a marked decrease of Bcl-2 and Bcl-xL protein expression. MTH-3 also decreased the protein levels of Ero1, PDI, PERK and calnexin, as well as increased the expression of IRE1α, CHOP and Bip that consequently led to ER stress and MDA-MB-231 cell apoptosis. In addition, MTH-3-treated cells were involved in the autophagic process and cleavage of LC3B was observed. MTH-3 enhanced the protein levels of LC3B, Atg5, Atg7, Atg12, p62 and Beclin-1 in MDA-MB-231 cells. Finally, DNA microarray was carried out to investigate the level changes of gene expression modulated by MTH-3 in MDA-MB-231 cells. Taken together, our results suggest that MTH-3 might be a novel therapeutic agent for the treatment of triple-negative breast cancer in the near future

eRitxi. Gestor de continguts multimèdia pel Grup SEGRE

Aplicatiu web de gestió i millora d'arxius xml per la publicació d'un diari digital multimèdia. Aquesta eina llegeix una estructura xml d'informació i la modifica, afegint arxiu multimèdia i altres opcions de visualització per millorar-ne l'ús com a diari digital multimèdia

Women Under Kuomintang R ule Variations on the Feminine Mystique

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/68360/2/10.1177_009770047500100101.pd

WDHD1 modulates the post-transcriptional step of the centromeric silencing pathway

The centromere is a highly specialized chromosomal element that is essential for chromosome segregation during mitosis. Centromere integrity must therefore be properly preserved and is strictly dependent upon the establishment and maintenance of surrounding chromatin structure. Here we identify WDHD1, a WD40-domain and HMG-domain containing protein, as a key regulator of centromere function. We show that WDHD1 associates with centromeres in a cell cycle-dependent manner, coinciding with mid-to-late S phase. WDHD1 down-regulation compromises HP1α localization to pericentric heterochromatin and leads to altered expression of epigenetic markers associated with this chromatin region. As a consequence, such reduced epigenetic silencing is manifested in disrupted heterochromatic state of the centromere and a defective mitosis. Moreover, we demonstrate that a possible underlying mechanism of WDHD1’s involvement lies in the proper generation of the small non-coding RNAs encoded by the centromeric satellite repeats. This role is mediated at the post-transcriptional level and likely through stabilizing Dicer association with centromeric RNA. Collectively, these findings suggest that WDHD1 may be a critical component of the RNA-dependent epigenetic control mechanism that sustains centromere integrity and genomic stability