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To investigate the spatio-temporal distribution characteristics and changing trends of syphilis in Nantong city. Joinpoint regression model, spatial autocorrelation and SaTScan spatio-temporal scanning were used to analyze the trend of syphilis reported incidence and spatio-temporal distribution characteristics in Nantong City. From 2013 to 2022, the reported incidence of syphilis in Nantong City increased at an average annual rate of 6.60%, of which the increase rate of latent syphilis was 13.45%. The high-high clustering areas were mainly distributed in 15 streets of Chongchuan District and all streets of Nantong Development Zone. SaTScan spatio-temporal scanning detected a total of two clustering areas, all from 2021 to 2022. The first cluster includes 24 streets with a radius of 16.27 km, and the second cluster includes 18 streets within a radius of 34.90 km. The reported incidence of syphilis in Nantong City showed an increasing trend, mainly manifested as an increase in latent syphilis, and the reported incidence of syphilis in various towns (streets) showed obvious spatial clustering, and attention should be paid to key areas and targeted interventions should be formulated.

The endothelial to mesenchymal transition (EndMT) plays a major role in cancer metastasis by regulating the complexity of the tumor microenvironment (TME). Here, we investigated whether 27-hydroxycholesterol (27HC) induces EndMT in endothelial cells (ECs). EndMT markers in the human microvascular endothelial cell-1 (HMEC-1) cell line and human umbilical vein endothelial cells (HUVECs) stimulated with 27HC were evaluated with Western blot. Epithelial to mesenchymal transition (EMT) markers in breast cancer (BC) cells cultured in conditioned medium were investigated with quantitative real time polymerase chain reaction (qRT-PCR). The MMP-2 and MMP-9 mRNA expression and activity were detected with qRT-PCR and gelatin zymography assays, respectively. The effect of activated STAT3 on 27HC-induced EndMT was validated by Western blot, immunofluorescence staining, and cell transfection assays. The migration ability of BC cells was evaluated with Transwell assays. We found that 27HC induced EndMT in HMEC-1 and HUVECs, and 27HC-induced EndMT facilitated EMT and BC cell migration. The 27HC-induced EMT of BC cells also promoted EndMT and HUVEC migration. Investigation of the underlying molecular mechanisms revealed that STAT3 knockdown repressed EndMT in HUVECs as well as migration in BC cells induced with 27HC. In addition, C646 and resveratrol, inhibitors of STAT3 acetylation, repressed the expression of Ac-STAT3, p-STAT3, and EndMT markers in HUVECs exposed to 27HC; these HUVECs in turn attenuated the migration ability of BC cells in 27HC-induced EndMT. Cross-talk between 27HC-induced EndMT and EMT was observed in the TME. Moreover, activation of STAT3 signaling was found to be involved in 27HC-induced EndMT.

Enhancer of zeste homolog 2 (EZH2) is frequently overexpressed in breast cancer and plays an important role in maintaining the cell proliferative capacity. However, the mechanisms underlying the transcriptional regulation of EZH2 in estrogen receptor (ER)-positive breast cancer cells remain unclear. The antitumor effects of resveratrol have been reported. However, whether EZH2 was involved in these effects needs further exploration. Here, we showed that EZH2 is required for estrogen-induced cell proliferation in ER-positive breast cancer. Exposure to 17β-estradiol (E2) upregulated EZH2 via ERα signaling, and this effect was blocked by U0126, a MEK inhibiter. Resveratrol inhibited the proliferation and colony formation in ER-positive breast cancer cells and downregulated EZH2 through inhibition of phospho-ERK1/2. These findings indicated that ERK1/2 and ER signaling–mediated EZH2 upregulation is crucial for the proliferation of ER-positive breast cancer cells. The suppression of EZH2 expression by ERK1/2 dephosphorylation is important for the antiproliferative activities of resveratrol against ER-positive breast cancer cells.

Endothelial-mesenchymal transition (EndMT) is the transformation of endothelial cell morphology to mesenchymal cell morphology, accompanied by decline of endothelial function and enhancement of mesenchymal function, which promotes tumor progression and tumor cell invasion and metastasis. 27-Hydroxycholesterol (27-HC) is a cholesterol metabolite, which has a high content in human blood. 27-HC promotes breast cancer cell proliferation, invasion, and migration. We previously showed that 27-HC promotes EndMT; however, the underlying mechanism still needs to be further explored. We studied the role of the 14-3-3η/GSK-3β/β-catenin complex in EndMT. Our results show that 27-HC induces oxidative stress in HUVECs and activates the p38 signaling pathway, thereby inhibiting the binding of 14-3-3η/GSK-3β/β-catenin, promoting the increase of free β-catenin and nuclear translocation, and finally inducing EndMT. Treatment with N-acetylcysteine (NAC) blocked 27-HC-induced ROS generation and p38 signaling pathway activation, prevented β-catenin from release from binding, and inhibited EndMT. Blocking ROS production or p38 signaling or knocking down 14-3-3η inhibited 27-HC-induced EndMT and inhibited breast cancer cell metastasis. These findings indicate 14-3-3η is necessary for interactions between the p38 kinase and the GSK-3β/β-catenin complex and serves as an adaptor to transmit the upstream kinase signal to the downstream signal, thereby promoting EndMT and breast cancer cell migration.

Flowering plants have evolved numerous intraspecific and interspecific prezygotic reproductive barriers to prevent production of unfavourable offspring 1 . Within a species, self-incompatibility (SI) is a widely utilized mechanism that rejects self-pollen 2 , 3 to avoid inbreeding depression. Interspecific barriers restrain breeding between species and often follow the SI × self-compatible (SC) rule, that is, interspecific pollen is unilaterally incompatible (UI) on SI pistils but unilaterally compatible (UC) on SC pistils 1 , 4 – 6 . The molecular mechanisms underlying SI, UI, SC and UC and their interconnections in the Brassicaceae remain unclear. Here we demonstrate that the SI pollen determinant S -locus cysteine-rich protein/ S -locus protein 11 (SCR/SP11) 2 , 3 or a signal from UI pollen binds to the SI female determinant S -locus receptor kinase (SRK) 2 , 3 , recruits FERONIA (FER) 7 – 9 and activates FER-mediated reactive oxygen species production in SI stigmas 10 , 11 to reject incompatible pollen. For compatible responses, diverged pollen coat protein B-class 12 – 14 from SC and UC pollen differentially trigger nitric oxide, nitrosate FER to suppress reactive oxygen species in SC stigmas to facilitate pollen growth in an intraspecies-preferential manner, maintaining species integrity. Our results show that SRK and FER integrate mechanisms underlying intraspecific and interspecific barriers and offer paths to achieve distant breeding in Brassicaceae crops. A signalling mechanism ensuring intraspecies and interspecies reproductive barriers in flowering plants is uncovered.

The superheated steam temperature (SST) suffers from complex dynamic characteristics such as nonlinearity and large time delay. To deal with the negative effects, this paper proposes a cascade predictive control strategy (CPC-PI) based on interval type-2 fuzzy neural network (IT2FNN) to improve the performance of SST. First, this paper proposes the IT2FNN model for modeling the SST model. And then on the basis the local linearized IT2FNN model, the CPC-PI strategy is designed. In the following, fuzzy self-regulation of the weight factor in the CPCPI is carried out to further improve the dynamic response speed and stability of SST. Finally, the comparative simulations verify that the IT2FNN-based CPC-PI control strategy with self-regulated weight factor is superior to the PI-PI control strategy and the IT2FNN-based CPC-PI control strategy with fixed weight factor.

Selecting the minimal best subset out of a huge number of factors for influencing the response is a fundamental and very challenging NP-hard problem because the presence of many redundant genes results in over-fitting easily while missing an important gene can more detrimental impact on predictions, and computation is prohibitive for exhaust search. We propose a modified memetic algorithm (MA) based on an improved splicing method to overcome the problems in the traditional genetic algorithm exploitation capability and dimension reduction in the predictor variables. The new algorithm accelerates the search in identifying the minimal best subset of genes by incorporating it into the new local search operator and hence improving the splicing method. The improvement is also due to another two novel aspects: (a) updating subsets of genes iteratively until the no more reduction in the loss function by splicing and increasing the probability of selecting the true subsets of genes; and (b) introducing add and del operators based on backward sacrifice into the splicing method to limit the size of gene subsets. Additionally, according to the experimental results, our proposed optimizer can obtain a better minimal subset of genes with a few iterations, compared with all considered algorithms. Moreover, the mutation operator is replaced by it to enhance exploitation capability and initial individuals are improved by it to enhance efficiency of search. A dataset of the body weight of Hu sheep was used to evaluate the superiority of the modified MA against the genetic algorithm. According to our experimental results, our proposed optimizer can obtain a better minimal subset of genes with a few iterations, compared with all considered algorithms including the most advanced adaptive best-subset selection algorithm.

Background: Thoracic aortic dissection is an emergent life-threatening condition. Routine screening for genetic variants causing thoracic aortic dissection is not currently performed for patients or their family members. Methods: We performed whole exome sequencing of 240 patients with thoracic aortic dissection (n=235) or rupture (n=5) and 258 controls matched for age, sex, and ancestry. Blinded to case-control status, we annotated variants in 11 genes for pathogenicity. Results: Twenty-four pathogenic variants in 6 genes (COL3A1, FBN1, LOX, PRKG1, SMAD3, TGFBR2) were identified in 26 individuals, representing 10.8% of aortic cases and 0% of controls. Among dissection cases, we compared those with pathogenic variants to those without and found that pathogenic variant carriers had significantly earlier onset of dissection (41 vs. 57 years), higher rates of root aneurysm (54% vs. 30%), less hypertension (15% vs. 57%), lower rates of smoking (19% vs. 45%), and greater incidence of aortic disease in family members. Multivariable logistic regression showed significant risk factors associated with pathogenic variants are age <50 [odds ratio (OR) = 5.5; 95% CI: 1.6-19.7], no history of hypertension (OR=5.6; 95% CI: 1.4-22.3) and family history of aortic disease (mother: OR=5.7; 95% CI: 1.4-22.3, siblings: OR=5.1; 95% CI 1.1-23.9, children: OR=6.0; 95% CI: 1.4-26.7). Conclusions: Clinical genetic testing of known hereditary thoracic aortic dissection genes should be considered in patients with aortic dissection, followed by cascade screening of family members, especially in patients with age-of-onset of aortic dissection <50 years old, family history of aortic disease, and no history of hypertension.