The diagnostic value of BI-RADS grade 3 to 5 for breast masses is correlated with the expression of estrogen receptor, progesterone receptor, human epidermal growth factor receptor-2.

BACKGROUND: The breast imaging-reporting and data system (BI-RADS) grading has a great advantage in diagnosing breast diseases, but with some limitations. AIMS: The study analyzed the value of ultrasound-guided core needle biopsy (CNB) in diagnosing BI-RADS grades 3, 4, and 5 breast cancer. METHODS: Breast cancer patients at BI-RADS grades 3 to 5 received breast ultrasonography, ultrasound-guided CNB and immunohistochemical examination. Receiver operating characteristic (ROC) curve was made to test diagnostic efficiency of regression model. RESULTS: Calcification was positively correlated with expression of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor (HER)-2. The areas of 4 ROC curves were 0.752, 0.805, 0.758, and 0.847, and the 95%CI was 0.660 to 0.844, 0.723 to 0.887, 0.667 to 0.849, and 0.776 to 0.918, respectively. BI-RADS grades 3 to 5 were positively correlated with expression of ER, PR and human epidermal growth factor receptor-2 (HER-2). Statistical significance existed between grade 5 and expression of ER, PR and HER-2, and between grade 4 and expression of HER-2. CONCLUSIONS: The study demonstrates that BI-RADS can be used as an effective evaluation method in the diagnosis of breast diseases before invasive operation, and it has higher diagnostic accuracy if combined with pathological examinations.

LINC02381, a sponge of miR-21, weakens osteogenic differentiation of hUC-MSCs through KLF12-mediated Wnt4 transcriptional repression.

INTRODUCTION: Human umbilical cord blood-derived MSCs (hUC-MSCs) have the potential to differentiate into osteoblasts. This study investigated the function and potential mechanisms of a novel lncRNA LINC02381 in hUC-MSC osteogenic differentiation. MATERIALS AND METHODS: hUC-MSCs were maintained in osteogenic differentiation medium. RT-qPCR assay was performed to assess LINC02381 expression. Alizarin Red S (ARS) and alkaline phosphatase (ALP) staining were performed to evaluate osteogenic differentiation. The interaction between miR-21 and LINC0238/KLF12 was determined by luciferase reporter and RNA immunoprecipitation (RIP) assays. Chromatin immunoprecipitation (ChIP) assay was used to confirm the transcriptional regulation of KLF12 on Wnt4 promoter. The nuclear translocation of ß-catenin was evaluated using immunofluorescence. hUC-MSCs seeded on Bio-Oss Collagen scaffolds were transplanted into nude mice to assess in vivo osteogenesis. Bone formation was observed by H&E and Masson's trichrome staining. OSX and OPN levels were assessed by immunohistochemistry. RESULTS: LINC02381 was up-regulated in the clinical samples of osteoporotic patients. However, LINC02381 expression was reduced during osteogenic differentiation of hUC-MSCs. Enforced expression of LINC02381 suppressed the osteogenic differentiation of hUC-MSCs. Mechanistically, LINC02381 sponged miR-21 to enhance KLF12 expression, which led to the inactivation of Wnt/ß-catenin signaling pathway. Furthermore, miR-21 mimics or KLF12 silencing counteracted LINC02381-induced inhibition of osteogenic differentiation, whereas IWP-4 (an inhibitor of Wnt pathway) abolished this effect. CONCLUSION: In summary, LINC02381 repressed osteogenic differentiation of hUS-MSCs through sponging miR-21 to enhance KLF12-mediated inactivation of Wnt/ß-catenin pathway, indicating that LINC02381 might be a therapeutic target for osteoporosis.

Fabrication of graphitic carbon nitride functionalized P-CoFe2O4 for the removal of tetracycline under visible light: Optimization, degradation pathways and mechanism evaluation.

In this study, nano-sized CoFe2O4 composites were prepared through co-precipitation process. Then the phosphorus-doped strong magnetic graphitic carbon nitride hybrids composites (P-CoFe2O4@GCN) was stemmed from the CoFe2O4 composites via the thermal polymerization method. The TEM results show that the CoFe2O4 nanoparticles have been successfully embedded into the graphitic carbon nitride (GCN). The BET specific surface area of P-CoFe2O4@GCN-1 could reach 36.91 m2/g, which was 5.38 times higher than that of GCN. Thus, it provided sufficient reaction active sites to enhance the photocatalytic activity for tetracycline (TC) decomposition. The results from the photocatalytic experiments showed that the degradation efficiency of TC by P-CoFe2O4@GCN-1 could reach 96.2% within 60 min, which is 3.19 times higher than that of GCN. The h+, O2•- and •OH radicals detected by the electron spin resonance (ESR) were responsible for the TC decomposition in the photocatalytic reaction system. Persulfate (PS) can further activate the hybrid mixture system, and the fitting model predicted by the response surface methodology (RSM) indicated that the maximum tetracycline removal could reach 99.6% within 30 min. In addition, the degradation intermediates of TC were detected by HPLC-MS and the photodegradation mechanism was discussed.

Carbon quantum dots decorated heteroatom co-doped core-shell Fe0@POCN for degradation of tetracycline via multiply synergistic mechanisms.

In this study, novel core-shell catalyst with a new ternary heterostructure was synthesized (Fe0@POCN/CQDs) for the degradation of tetracycline (TC). The TEM results showed that the Fe0 particles were wrapped in POCN material and many nano CQDs were uniformly dispersed in the material. The new ternary nanocomposite exhibits excellent photocatalytic activity for the removal of TC, which was approximately 4.76 times higher than that of GCN. The enhancement of photocatalytic activity was attributed to the effective heterojunction as well as the multiply synergistic effects of POCN combined with Fe0 and CQDs, which was beneficial for retardation of recombination rate of photogenerated electron-hole pairs and generation of more free radicals for the oxidation of TC. Besides, the reactive oxygen species (ROS) of h+, •O2- and •OH played pivotal roles in the degradation of TC by Fe0@POCN/CQDs during the photocatalytic reaction. At the same times, sulfate radical (SO4•-) and hydroxyl radical (•OH) highlighted the dominant role in the degradation process compared with other free radicals under persulfate hybrid mixture system (PS system), which was further confirmed by radical scavenger experiments and electron spin resonance (ESR) analysis. The response surface methodology (RSM) study indicated that the optimal removal parameters of tetracycline could reach 97.57% within 30 min under PS system. In addition, the possible degradation pathway intermediates of TC were studied by HPLC-MS and the reaction catalytic activity mechanism of Fe0@POCN/CQDs/persulfate system was discussed.

In situ fabrication of hierarchical biomass carbon-supported Cu@CuO-Al2O3 composite materials: synthesis, properties and adsorption applications.

Hierarchical Cu-Al2O3/biomass-activated carbon composites were successfully prepared by entrapping a biomass-activated carbon powder derived from green algae in the Cu-Al2O3 frame (H-Cu-Al/BC) for the removal of ammonium nitrogen (NH4 +-N) from aqueous solutions. The as-synthesized samples were characterized via XRD, SEM, BET and FTIR spectroscopy. The BET specific surface area of the synthesized H-Cu-Al/BC increased from 175.4 m2 g-1 to 302.3 m2 g-1 upon the incorporation of the Cu-Al oxide nanoparticles in the BC surface channels. The experimental data indicated that the adsorption isotherms were well described by the Langmuir equilibrium isotherm equation and the adsorption kinetics of NH4 +-N obeyed the pseudo-second-order kinetic model. The static maximum adsorption capacity of NH4 +-N on H-Cu-Al/BC was 81.54 mg g-1, which was significantly higher than those of raw BC and H-Al/BC. In addition, the presence of K+, Na+, Ca2+, and Mg2+ ions had no significant impact on the NH4 +-N adsorption, but the presence of Al3+ and humic acid (NOM) obviously affected and inhibited the NH4 +-N adsorption. The thermodynamic analyses indicated that the adsorption process was endothermic and spontaneous in nature. H-Cu-Al/BC exhibited removal efficiency of more than 80% even after five consecutive cycles according to the recycle studies. These findings suggest that H-Cu-Al/BC can serve as a promising adsorbent for the removal of NH4 +-N from aqueous solutions.