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1.
Chem Commun (Camb) ; 59(16): 2327, 2023 Feb 21.
Article in English | MEDLINE | ID: mdl-36762514

ABSTRACT

Correction for 'Controlling CO2 hydrogenation selectivity by Rh-based catalysts with different crystalline phases of TiO2' by Fenghai Cao et al., Chem. Commun., 2022, 58, 4219-4222, https://doi.org/10.1039/D2CC00472K.

2.
Anal Chim Acta ; 1223: 340218, 2022 Aug 29.
Article in English | MEDLINE | ID: mdl-35999005

ABSTRACT

Accurate detection of microRNA (miRNA) is challenging but essential for disease diagnostics and therapeutics. To meet the high demands of miRNA analysis, we proposed a highly sensitive and specific electrochemical strategy based on duplex-specific nuclease (DSN)-assisted target recycling and DNA self-assembled FeNxC nanocatalytic network for precise quantitation of miRNA-21 as a model. FeNxC nanospherical catalyst with high peroxidase-mimicking activity was synthesized through high-temperature pyrolysis and modified with DNA. The identification of miRNA-21 by elaborately designed capture probe triggered DSN-assisted target recycling. Subsequently, self-assembled FeNxC nanocatalytic network was constructed on the sensor surface through DNA hybridization reaction, whose signal response was demonstrated to be 4.272-fold higher than the single layer of FeNxC. By virtue of such cascade signal amplification, ultrasensitive electrochemical detection of miRNA-21 was realized in a dynamic range of 0.5 fM - 1 pM with a detection limit of 0.2805 fM. Additionally, the proposed strategy exhibited high specificity for miRNA-21 and practical applicability in real sample analysis, demonstrating promising potential for the reliable miRNA analysis in disease diagnosis and therapy applications.


Subject(s)
Biosensing Techniques , MicroRNAs , DNA/genetics , Electrochemical Techniques , Endonucleases/metabolism , Limit of Detection , MicroRNAs/analysis , Nucleic Acid Hybridization
3.
Chem Commun (Camb) ; 58(26): 4219-4222, 2022 Mar 29.
Article in English | MEDLINE | ID: mdl-35274644

ABSTRACT

A series of Rh-based catalysts with various crystalline phases (p25, anatase, and rutile) were prepared via the incipient-wetness impregnation method. It was found that these catalysts had different metal-support interactions. Hence, 1%Rh/p, 1%Rh/r, and 1%Rh/a exhibited methane, CO, and methanol selectivity, respectively.

4.
Exp Ther Med ; 22(5): 1310, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34630664

ABSTRACT

Colorectal cancer ranks third in terms of incidence and second in terms of mortality worldwide. The homeobox transcript antisense intergenic RNA (HOTAIR), which was found to be located on the antisense chain of the homeobox C (HOXC) gene cluster, is a long non-coding RNA involved in multiple types of tumors. The role of HOXC11 in tumors remains unclear. Reverse transcription-quantitative PCR was performed to detect the expression level of HOXC11 in colon adenocarcinoma. Cell proliferation and invasion were assessed. RNase protection assay was used to test the possibility of RNA duplex formation. The increased expression and co-expression trend of HOXC11 and HOTAIR were identified in multiple types of cancer from The Cancer Genome Atlas and the results were validated in 12 colon adenocarcinoma and paired non-tumor tissue samples. The expression of HOXC11 and HOTAIR was found to be associated with poor prognosis in colon adenocarcinoma and kidney renal clear cell carcinoma. Furthermore, HOXC11 was found to positively regulate HOTAIR by RNA duplex formation and promoted the proliferation and invasion of colon adenocarcinoma cells.

5.
Nat Prod Res ; 34(4): 489-493, 2020 Feb.
Article in English | MEDLINE | ID: mdl-30369253

ABSTRACT

(±)-Quassidine K (1), a pair of new bis-ß-carboline alkaloid enantiomers, were isolated from Picrasma quassioides. Their structures were determined on the basis of detailed spectroscopic data analysis. The absolute configurations of (+)-S-quassidine K (1a) and (-)-R-quassidine K (1b) were determined by comparing with the reported experimental ECD spectra after chiral separation. The cytotoxicity assay showed activity against HeLa cells with IC50 values of 15.8 and 20.1 µM, respectively.


Subject(s)
Alkaloids/isolation & purification , Antineoplastic Agents/isolation & purification , Carbolines/isolation & purification , Picrasma/chemistry , Alkaloids/chemistry , Alkaloids/pharmacology , Antineoplastic Agents/pharmacology , Carbolines/chemistry , Carbolines/pharmacology , Drug Screening Assays, Antitumor , HeLa Cells , Humans , Inhibitory Concentration 50 , Molecular Structure , Stereoisomerism
6.
Chemistry ; 25(1): 189-194, 2019 Jan 02.
Article in English | MEDLINE | ID: mdl-30351453

ABSTRACT

Converting renewable biomass and their derivatives into chemicals and fuels has received much attention to reduce the dependence on fossil resources. Photocatalytic ethanol dehydrogenation-acetalization to prepare value-added 1,1-diethoxyethane and H2 was achieved over non-precious metal CdS/Ni-MoS2 catalyst under visible light. The system displays an excellent production rate and high selectivity of 1,1-diethoxyethane, 52.1 mmol g-1 h-1 and 99.2 %, respectively. In-situ electron spin resonance, photoluminescence spectroscopy and transient photocurrent responses were conducted to investigate the mechanism. This study provides a promising strategy for a green application of bioethanol.

7.
J Cancer ; 9(12): 2123-2131, 2018.
Article in English | MEDLINE | ID: mdl-29937931

ABSTRACT

Background: Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) have been demonstrated to mitigate radiation-induced lung damage in animal models and preclinical studies. Our study aims to evaluate whether ACEIs or ARBs reduce the incidence of radiation-induced pneumonitis (RP) in lung cancer patients. Methods: Publications were searched from EMBASE, PubMed and Web of Science databases. Seven studies published from April 2000 to August 2016 met inclusion criteria and included 1412 patients in total. Only patients with grade 2 and above pneumonitis within 12 months after radiotherapy were analyzed. Results: Patients taking ACEIs had a lower risk of developing radiation pneumonitis compared with non-users (OR = 0.46, 95%CI = 0.31-0.67, p < 0.0001). While the use of ARBs couldn't reduce the incidence of RP (OR = 1.42, 95%CI = 0.94-2.14, p = 0.10). Elderly patients (age ≥ 70) benefited more from ACEIs (OR = 0.12, 95%CI = 0.02-0.67, p = 0.02). In addition, smokers were found to have a lower risk of developing RP than non-smokers (OR = 0.49, 95%CI = 0.30-0.81, p = 0.005), but sex and the use of statin or NSAID had no influence on the appearance of RP (p = 0.59, p = 0.70, p = 0.40, respectively). Conclusions: ACE inhibitors could decrease the incidence of symptomatic RP among lung cancer patients. However, the use of ARBs has a slight trend to develop RP but not above statistical significance. Elderly patients (age ≥ 70) benefited the most from ACEIs.

8.
Int J Biol Macromol ; 116: 545-551, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29753015

ABSTRACT

Recently, lncRNA ZEB2-AS1 was identified as a lncRNA that promoted cancer progression. However, the biological function and the underlying mechanism of ZEB2-AS1 in pancreatic cancer had not been reported. In the current study, we revealed that the expression level of ZEB2-AS1 was elevated in pancreatic cancer cell lines and tissues. ZEB2-AS1 inhibition decreased cell growth and invasion in pancreatic cancer. Mechanismly, ZEB2-AS1 exerted as a ceRNA and negatively regulated miR-204 expression. In addition, HMGB1 was identified as a down-stream target of miR-204. The miR-204/HMGB1 axis mediated ZEB2-AS1's effect on pancreatic cancer. Our findings revealed that lncRNA ZEB2-AS1 may be a candidate prognostic biomarker and a target for new therapies in pancreatic cancer patients.


Subject(s)
Biomarkers, Tumor/biosynthesis , Cell Proliferation , HMGB1 Protein/biosynthesis , MicroRNAs/biosynthesis , Neoplasm Proteins/biosynthesis , Pancreatic Neoplasms/metabolism , RNA, Long Noncoding/biosynthesis , RNA, Neoplasm/biosynthesis , Biomarkers, Tumor/genetics , Cell Line, Tumor , Female , HMGB1 Protein/genetics , Humans , Male , MicroRNAs/genetics , Neoplasm Invasiveness , Neoplasm Proteins/genetics , Pancreatic Neoplasms/genetics , Pancreatic Neoplasms/pathology , RNA, Long Noncoding/genetics , RNA, Neoplasm/genetics
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