Notes

[Computed tomography-based radiomics pertaining to differential of retroperitoneal neuroblastoma and ganglioneuroblastoma within children].
We aimed to evaluate whether the overall harmful effect of periprocedural treatment with aspirin or heparin during endovascular stroke treatment is different in patients with a successful reperfusion after the procedure.

We performed a post-hoc analysis of the MR CLEAN-MED trial, including adult patients with a large vessel occlusion in the anterior circulation eligible for endovascular treatment (EVT). In this trial, patients were randomized for periprocedural intravenous treatment with aspirin or no aspirin (11 ratio), and for moderate-dose unfractionated heparin, low-dose unfractionated heparin or no unfractionated heparin (111 ratio). We tested for interaction between the post-EVT extended thrombolysis in cerebral infarction (eTICI) score and treatment with periprocedural medication with multivariable regression analyses. The primary outcome was the modified Rankin Scale score at 90 days. Secondary outcomes were final infarct volume, intracranial hemorrhage, and symptomatic intracranial hemorrhage.

Of 534 included patients, 93 (17%) had a post-EVT eTICI score of 0-2a, 115 (22%) a score of 2b, 73 (14%) a score of 2c, and 253 (47%) a score of 3. For both aspirin and heparin, we found no interaction between post-EVT eTICI score and treatment on the modified Rankin Scale score (p=0.76 and p=0.47, respectively). We found an interaction between post-EVT eTICI score and treatment with heparin on the final infarct volume (p=0.01). Of note, this interaction showed a biologically implausible distribution over the subgroups.

The overall harmful effect of periprocedural aspirin and unfractionated heparin is not different in patients with a successful reperfusion after EVT.
The overall harmful effect of periprocedural aspirin and unfractionated heparin is not different in patients with a successful reperfusion after EVT.N6-methyladenosine (m6A) in RNAs is closely related to various biological progresses, but the specific regulatory mechanisms are still unclear. The existing m6A single-base resolution analysis techniques have problems of specificity and sensitivity to be improved, which can hardly meet the urgent needs of basic research and clinical applications. This work proposes a new strategy based on xeno nucleic acid (XNA) probe and CRISPR/Cas12a signal amplification for the sensitive detection of site-specific m6A modifications. According to the difference in the thermodynamic stability of hybridization between XNA probe with m6A-RNA and A-RNA, XNA was designed as a block probe to mediate m6A-RNA specific reverse transcription polymerase chain reaction (MsRT-PCR). Therefore, m6A can be specifically distinguished by converting difficult-to-test m6A modifications into easily detectable dsDNA fragments. Integration of CRISPR/Cas12a technology, skilfully designed sequences of crRNAs targeting m6A site-specific amplification dsDNA. The specificity was significantly improved through dual specific recognition of XNA probe and crRNA. Furthermore, the sensitivity of the assay was also greatly increased by the combined signal amplification of PCR and CRISPR/Cas12a. Additionally, we extend the application of CRISPR/Cas12a to flexible fluorescent and electrochemical biosensing system, which can accurately detect m6A modifications with different ranges of methylation fractions. find more The analysis results of m6A sites in MALAT1, ACTB and TPT1 further demonstrated the feasibility of the constructed biosensor for the accurate detection of hypomethylated samples in cells. The implementation of this work will provide strong technical support to promote the in-depth research on m6A in disease regulation mechanisms and in vitro molecular diagnosis.Novel magnetic and fluorinated porous carbons (M-FPCs) with high fluorine content, large pore volume and specific surface area were first prepared by carbonizing and further fluorinating Fe-Zr bimetal-organic frameworks. The M-FPCs exhibit excellent adsorption performance toward perfluorinated compounds (PFCs), and the maximal adsorption capacity ranges from 518.1 to 919.3 mg g-1 for various PFCs. Based on this property, an environmental analytical method of dispersive solid-phase extraction (DSPE) using M-FPCs as adsorbents coupled with ultra-high-performance liquid chromatography-mass spectrometry (UPLC-MS) was developed for the detection of trace PFCs. The linear range was as wide as 10-200 ng L-1, and low limit of detection (0.02-0.16 ng L-1) and good precision (relative standard deviation less than 6.11% for intra-day and inter-day) were achieved. This method was applied to the detection of trace PFCs in environmental water and soil samples with satisfactory results.Organophosphorus compounds such as chlorpyrifos (CPS) are causing serious environmental problems worldwide. Efficient monitoring of the CPS levels in water resources demands portable devices for on-field testing. Here we report the development of a CPS sensor coupled with smartphones for automated reading and data analysis. The sensing mechanism makes use of gold nanoparticles stabilized by a CPS-specific aptamer, where colloidal destabilization occurs in presence of competing CPS molecules. In particular, an innovative readout is proposed quantitative analysis of the stain patterns left by evaporating drops of the test solutions. We have found that the CPS-induced destabilization suppresses the typical coffee-ring stain of the colloidal gold, and then exploited the phenomenon to quantitatively determine the CPS concentration in water samples. A strong correlation between CPS level in samples and the alteration of the stain patterns was established for a wide range of CPS concentrations (0.048 μM-482 μM). The limit of detection of the sensor was 0.2 μM. The assay was implemented on Whatman filter paper cards that were specially patterned by wax-printing. A smartphone-based Python program was written for fully automated image capture and processing. Notably, as we analyze the spatial configuration of the stains, the reading system is independent of external illumination. The system also enables data management and traceability, which are highly desirable attributes for environmental monitoring.Nucleus pH is closely linked to many diseases such as aging, heart disease, skeletal myopathies, cancer, Alzheimer's disease, etc. Nevertheless, fluorescent sensors that can directly monitor nucleus pH changes have not yet been reported. Here, we first reported a green emissive carbon dots (CDs) for nucleus pH detection in living cells. CDs can selectively target nucleus with high accumulation at nucleolus due to their high affinity towards RNA once entering cells by lipid raft mediated endocytosis. Without washing, CDs at 5 μg/mL was enough to lighten nucleus within 10 min with the fluorescence on ever after 24 h incubation, achieving fast, wash-free, and long-term nucleus/nucleolus imaging. Meanwhile, the luminescent intensity of CDs was reduced gradually when pH changed continuously from 1 to 12, showing a pH-responsive fluorescence property with two linear ranges of pH 2-7 and pH 7-12. With their nucleus-targeting ability and pH-dependent photoluminescent property, CDs was successfully leveraged for nucleus pH detection in A549 cells and for in vivo pH sensing in zebra fish. CDs present a promising and powerful fluorescent sensor for nucleus imaging and nucleus pH sensing in living cells on the way to understand nucleus-related biological events.Single particle inductively coupled plasma mass spectrometry (spICP-MS) has been explored for the determination of metallic nanoparticles (NPs) in air. Different extraction strategies (i.e., direct immersion, hard cap espresso, ultrasound-assisted and microwave-assisted extraction) and extracting solvents (i.e., citric acid, trisodium citrate, potassium nitrate, sodium nitrate, thiourea, disodium pyrophosphate and ammonium hydroxide) were investigated for platinum and gold NPs recovery from glass and microquartz fiber filters with a nominal size cut-off of 300 nm. Results show that metallic NPs are preserved and quantitatively extracted from the filter in 4 min inside an 800 W microwave oven by using 40 mL of a 2.0% w w-1 NH4OH solution. For the remaining extraction procedures, either incomplete recoveries or NPs degradation occur. As regards the influence of filter material, microquartz fiber affords better NPs capturing performance than glass fiber ones, enabling the quantification of NPs with diameters above 28 nm. This methodology has been successfully applied to determine PtNPs in filters from environmental monitoring stations and to gain insight into NPs transport through ICP-MS sample introduction system. Care should be taken during spICP-MS calibration since biased results might be obtained due to differences on NPs transport efficiency between standards and samples.Nucleic acid hybridization is occurred between the selective single-stranded nucleic acid sequence and its target sequence, which is one of the essential procedure for electrochemical detection of nucleic acid. microRNA-21 (miRNA-21) is known as a biomarker in various cancers. The determination of miRNA-21 was attained through by hybridization of inosine substituted miRNA-21 specific DNA probe (Pinosine) with its target miRNA-21. In this study, the surface of pencil graphite electrode (PGE) was firstly modified with halloysite nanoclay-ionic liquid (HNT/IL) nanocomposite. The characterization of surface was performed by Scanning Electron Microscope (SEM) images and Energy Dispersive X-Ray Analysis (EDX) analysis, and the differences at surface modifications were also shown by electrochemical methods with electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). For sensitive and selective determination of miRNA-21, Pinosine and target miRNA concentration, immobilization and hybridization time were optimized by using HNT/IL modified PGE in combination with differential pulse voltammetry (DPV). The detection limit was achieved as 0.17 μg/mL (equals to 23.69 nM) in the linear range of 0.25-2 μg/mL miRNA-21. The selectivity of voltammetric method based on HNT/IL-PGE developed for miRNA-21 was examined in the presence of mismatch (MM) and non-complementary (NC) sequences. Because miRNA-21 is over-expressed in cancer cells, it has been tested in total RNA samples isolated from cancer cell line (breast cancer cell line, MCF-7). In the total RNA samples obtained from MCF-7, the detection limit was calculated as 0.28 μg/mL in the linear range of 1-4 μg/mL. Besides, the healthy cell line (human embryonic kidney cell line, HEK-293) was used as a control group and the results obtained by MCF-7 total RNA samples were compared to the results using HEK-293 total RNA samples in terms of miRNA-21 level.Clear cell renal cell carcinoma (ccRCC) is known as the most aggressive subtype of genitourinary cancers. The lack of effective therapies has prompted us to further explore the complex network of genes involved in ccRCC tumor progression and metastasis and to seek new biomarkers and therapeutic strategies to improve clinical outcomes. Interleukin-1 receptor type 2 (IL1R2), a decoy receptor of IL-1, is found to be differentially expressed in various tumors types recently. However, the role of IL1R2 in ccRCC has not been documented. Herein, we found that the expression of IL1R2 in ccRCC tissues was significantly increased as the tumor's Furman pathological grade was elevated. Compared to lower IL1R2 expression, ccRCC patients with high IL1R2 expression had a significantly worse OS rate. IL1R2 could serve as an independent prognostic predictor for ccRCC patients. Depletion of IL1R2 could inhibit cell proliferation, migration, invasion, and cell cycle arrest at the G1 phase, while overexpression of IL1R2 could reverse this effect.
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