Background: Down-expression of microRNA-497 (miR-497) was often found in malignancies. The purposes of this study were to determine the expression of miR-497 in human osteosarcoma and to establish the association between miR-497 expression with cell survival and the sensitivity to cisplatin in human osteosarcoma cells. Methods: The effects of ectopic miR-497 expression on the cell survival and cisplatin sensitivity in osteosarcoma cells were measured by the Cell Counting Kit-8 (CCK-8) assay. Quantitative real-time PCR (qRT-PCR) was utilized to determine the expression of miR-497. The effects of ectopic miR-497 expression on the expression of VEGFA, Akt and p-Akt were determined by western blot. Results: Real-time quantitative PCR analysis revealed that miR-497 was significantly down-regulated in osteosarcoma tissues and in the osteosarcoma cell line SAOS-2 compared with adjacent nontumorous osteosarcoma tissues and normal human osteoblasts. Up-regulation of miR-497 inhibited cell survival and enhanced the sensitivity to cisplatin in osteosarcoma cells. In addition, knockdown of miR-497 induced osteosarcoma cells growth and cisplatin resistance. Luciferase reporter assay and western blot confirmed that VEGFA was a direct target of miR-497. PI3K inhibitor LY294002 abrogated miR-497 inhibitors induced cisplatin resistance. Conclusion: Taken together, our results suggest that miR-497 modulates the sensitivity to cisplatin at least in part through PI3K/Akt pathway in osteosarcoma cells.
MicroRNAs play important roles in the pathogenesis of cancers by inhibiting gene expression at posttranscriptional level. Here, we identified that miR-590 and its predicted target gene RB1 are differentially expressed in T-cell acute lymphoblastic leukaemia (T-ALL). The correlation between miR-590 and RB1 was further confirmed in 395 T-ALL patients. In T-ALL cell lines, miR-590 promoted the cell proliferation by increasing G1/S transition. Moreover, migration and invasion assay showed that miR-590 promotes the migration and invasion of T-ALL cells by increasing E-cadherin and inhibiting MMP-9. Luciferase assays confirmed that miR-590 directly binds to the 3′untranslated region of RB1, and western blotting showed that miR-590 suppresses the expression of RB1 at the protein levels. This study indicated that miR-590 inhibits RB1 and promotes proliferation and invasion of T-ALL cells. Thus, miR-590 may represent a potential therapeutic target for T-ALL intervention.
Objective
This study investigated the epidemiology, virulence and drug resistance of invasive
Klebsiella pneumoniae
(
K. pneumoniae
) isolates at a children’s medical center in eastern China in order to obtain epidemiologic, virulence, and antimicrobial resistance data that can guide for the selection and development of anti-infection treatments.
Methods
A total of 94 invasive
K. pneumoniae
strains were isolated from children between January 2016 and December 2020 at the Children’s Hospital of Soochow University. The strains were identified by mass spectrometry. The Kirby–Bauer method and VITEK 2 Compact system were used to analyze the antimicrobial susceptibility. Polymerase chain reaction (PCR) and sequencing was performed to detect the capsular serotypes, virulence-associated genes, β-lactam antibiotic resistance genes and multilocus sequence typing.
Results
The PCR results showed that 87 strains (92.55%) of invasive
K. pneumoniae
were hypervirulent capsular serotypes, with K57 as the dominant capsular serotype (62.77%). All strains carried virulence-associated genes. Among them, 84 strains (89.36%) carried hypervirulence genes, with
iroB
(86.17%) being the predominant; meanwhile, other virulence genes, including
wabG
(100.00%),
mrkD
(98.94%),
ycfM
(96.81%),
fimH
(95.74%) and
Uge
(88.30%), were detected in most strains. All strains carried β-lactam antibiotic resistance genes; the main extended-spectrum β-lactamase gene was
bla
SHV-11
(86.17%) and the major AmpC cephalosporinase genes were
bla
FOX-1
(86.17%) and
bla
ACT-1
(70.21%). Carbapenemase genes were detected in only a few isolates. Notably, 12 invasive
K. pneumoniae
isolates were identified as carbapenem-resistant and hypervirulent
K. pneumoniae
(CR-HVKP), and 14 other multidrug resistance (MDR) isolates were also detected.
Conclusion
The results of this study reveal the epidemiology, virulence and antimicrobial resistance of invasive
K. pneumoniae
in pediatric patients. Both CR-HVKP and MDR strains were identified, which should be of great concern to clinicians.
MicroRNA-340 (miR-340) was considered as a tumor suppressor by affecting cancer cell proliferation, apoptosis, invasion, and migration, and was downregulated in diverse cancers. Moreover, dysregulation of miR-340 was also found to be associated with drug resistance and predicted patients' survival in various cancers. Herein, we investigated miR-340 expression and its clinical significance in acute myeloid leukemia (AML). Real-time quantitative polymerase chain reaction was performed to detect miR-340 expression in bone marrow (BM) from 99 newly diagnosed AML patients except for acute promyelocytic leukemia (APL), 19 AML patients achieved complete remission (CR), and 29 healthy donors. BM miR-340 expression was significantly underexpressed in newly diagnosed AML patients as compared with controls (p = 0.031) and AML patients achieved CR (p = 0.025). No significant differences were observed between miR-340 expression and most of the clinicopathologic features (p > 0.05). However, low miR-340 expression was found to be associated with lower CR rate in both non-APL-AML and cytogenetically normal AML (CN-AML; p = 0.001 and 0.031, respectively), and acted as an independent risk factor for CR by logistic regression analysis (p = 0.001 and 0.021, respectively). More important, among both non-APL-AML and CN-AML, low expression of miR-340 was also associated with shorter overall survival (OS; p = 0.013 and 0.005, respectively), and was further validated by Cox regression (p = 0.031 and 0.039, respectively).Collectively, our study showed that BM miR-340 expression was downregulated in AML, and low expression of miR-340 correlated with adverse prognosis. K E Y W O R D S acute myeloid leukemia, expression, microRNA-340, prognosis J Cell Physiol. 2019;234:4200-4205. wileyonlinelibrary.com/journal/jcp 4200 |
Agricultural ecological efficiency is of great value to the government’s agricultural policy formulation. Research on the factors affecting agricultural ecological efficiency can provide support for the formation of countermeasures to improve agricultural ecological efficiency. Existing research has not conducted an in-depth analysis of the impact of urbanization on agricultural ecological efficiency, and there is a lack of relevant research on the impact of urbanization on agricultural ecological efficiency. This article is based on the data of 30 provinces and cities in China from 2009 to 2018, using the SBM model that considers undesired output, entropy method, Tobit model and other models and methods to measure agricultural ecological efficiency and urbanization comprehensive index, and analyze the impact of urbanization comprehensive index and urbanization indicators on agricultural ecological efficiency. The research results are as follows: 1) The overall agricultural ecological efficiency in China’s 30 provinces and cities has been increasing from 2009 to 2018. The eastern region has the highest agricultural ecological efficiency, followed by the western region, and the central and northeastern regions have relatively low values; 2) The comprehensive urbanization index of China’s 30 provinces and cities continued to grow from 2009 to 2018.The level of urbanization in the eastern region is the highest, in the central region has increased rapidly from 2009 to 2018, and in the western and northeastern regions is relatively low; 3) The overall increase in urbanization can promote the improvement of agricultural ecological efficiency. The impact of specific urbanization indicators on agricultural ecological efficiency is complex. Therefore, discussing the impact of urbanization on agricultural ecological efficiency cannot be considered from a single aspect, but should be analyzed from multiple perspectives.