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1.
Gastroenterol Rep (Oxf) ; 7(5): 354-360, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31687155

RESUMO

BACKGROUND: Hepatocellular carcinoma (HCC) is frequently associated with metabolism dysfunction. Increasing evidence has demonstrated the crucial role of lipid metabolism in HCC progression. The function of apolipoprotein F (ApoF), a lipid transfer inhibitor protein, in HCC is incompletely understood. We aimed to evaluate the functional role of ApoF in HCC in this study. METHODS: We used quantitative reverse-transcription polymerase chain reaction (qRT-PCR) to detect ApoF mRNA expression in HCC tissues and hepatoma cell lines (SMMC-7721, HepG2, and Huh7). Immunohistochemistry was performed to detect the expression of ApoF in HCC tissues. The associations between ApoF expression and clinicopathological features as well as HCC prognosis were analyzed. The effect of ApoF on cellular proliferation and growth of SMMC-7721 and Huh7 cells was examined in vitro and in vivo. RESULTS: ApoF expression was significantly down-regulated at both mRNA and protein levels in HCC tissues as compared with adjacent tissues. In SMMC-7721 and Huh7 HCC cells, ApoF overexpression inhibited cell proliferation and migration. In a xenograft nude mouse model, ApoF overexpression effectively controlled HCC growth. Kaplan-Meier analysis results showed that the recurrence-free survival rate of HCC patients with low ApoF expression was significantly lower than that of other HCC patients. Low ApoF expression was associated with several clinicopathological features such as liver cirrhosis, Barcelona Clinic Liver Cancer stage and tumor-node-metastasis stage. CONCLUSIONS: ApoF expression was down-regulated in HCC, which was associated with low recurrence-free survival rate. ApoF may serve as a tumor suppressor in HCC and be a potential application for the treatment of this disease.

2.
ACS Appl Mater Interfaces ; 6(2): 1207-12, 2014 Jan 22.
Artigo em Inglês | MEDLINE | ID: mdl-24372321

RESUMO

A silicon oxide film doped with fluorine was grown on a (100)-oriented Si wafer through liquid-phase deposition (LPD) as a protective mask of the wafer's rear side in order to chemically texture the wafer's unprotected front side in a basic etching bath, which is a new process in solar-cell manufacturing. The growth rate of the LPD-SiO2 film increased monotonically with an increase of the deposition temperature up to 60 °C for a given precursor solution. Field-emission scanning electron microscopy (FE-SEM) indicates that a pyramidal surface texture forms on the front side in the chemical texturing bath, whereas the underlying Si surface on the rear side remains intact. As a result, the average reflectivity for incident light over 450-850 nm is decreased to 11.1% on the front side, and a 5.8 µm thick Si surface on the rear side is saved per wafer. The all-wet process involved in this single-sided texturing is promising for the mass production of thinner and higher-efficiency Si-based solar cells because of its simplicity and lower cost.

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