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Diffuse large B-cell lymphoma (DLBCL) is a complex and aggressive malignancy originating from B lymphocytes and characterized by extensive clinical, phenotypic and molecular heterogeneity. Although research conducted over the past decades has substantially improved our understanding of DLBCL, its pathogenesis has not yet been fully elucidated. The development of RNA sequencing technology has allowed the identification of numerous long noncoding RNAs (lncRNAs) that exhibit aberrant expression in DLBCL. These lncRNAs play crucial roles in DLBCL development and pathogenesis and are thus good candidates for use as diagnostic biomarkers or therapeutic targets. In this review, we describe the lncRNAs associated with DLBCL, summarize their characteristics and molecular functions, and discuss their relationships with clinical practice. [ABSTRACT FROM AUTHOR]

Background: Canonical Wnt/β-catenin signaling is frequently dysregulated in acute myeloid leukemia (AML) and has been implicated in leukemogenesis. γ-catenin was previously demonstrated to be associated with the nuclear localization of β-catenin, the central mediator, and to exert oncogenic effects in AML; however, the underlying mechanisms remain unclear. Our study aimed to investigate the expression characteristics of γ-catenin in AML patients, explore the mechanisms by which γ-catenin regulates β-catenin, and discuss the feasibility of targeting γ-catenin for AML treatment. Methods: The mRNA expression levels of γ-catenin in AML patients were measured by qRT-PCR. Cell proliferation was examined via Cell Counting Kit-8 (CCK-8) assays. The expression levels of related proteins were measured via Western blotting. Specific siRNA was used to modulate the expression level of the γ-catenin gene. Apoptosis and cell cycle distribution were quantified by flow cytometry. The subcellular localization of γ-catenin and β-catenin was examined via immunofluorescence with a confocal laser scanning microscope. Results: Overexpression of γ-catenin was frequently observed in AML and correlated with poor prognosis. Consistent with this finding, suppression of γ-catenin in the AML cell line THP-1 induced growth inhibition, promoted apoptosis and blocked β-catenin nuclear translocation. Interestingly, γ-catenin knockdown sensitized THP-1 cells to cytotoxic chemotherapeutic agents such as cytarabine and homoharringtonine and further inhibited β-catenin nuclear localization. Moreover, our data implied the relationship between γ-catenin and GSK3β (whose effect on β-catenin is mediated by its own phosphorylation), which may be the principal mechanism underlying the anti-AML effect of γ-catenin inhibition. Conclusion: Taken together, our results revealed a potential role of γ-catenin in AML pathogenesis–mainly through the inhibition of GSK3β-mediated nuclear localization of β-catenin–and indicate that targeting γ-catenin might offer new AML treatments. [ABSTRACT FROM AUTHOR]

The trade-off between hardness and stretchability is a cornerstone of materials science. Balancing this trade-off is important in the molecular design of both chemical and physical networks. In this study, we report the quantitative trade-off at the molecular level for physical networks. Namely, we analyze, based on the reversible gelation model, a scaling relationship between the characteristic terminal relaxation modulus Gc in linear viscoelasticity and the stretch ratio λmax at the stress overshoot during the nonlinear elongation flow for unentangled randomly associative polymers, i.e., λmax ∼ Gc−0.17 and λmax ∼ Gc−0.33 in the mean-field and critical-percolation regimes, respectively. We use sulfonated polystyrene having different alkali counterions as a model system to test the relationship. The exponent of λmax ∼ Gc−0.25 seen in the experiment is in between the two theoretical values. We also discuss the quantitative deviation with respect to the size distribution of the network strands. [ABSTRACT FROM AUTHOR]

Anther-specific expression of OsRIP1 causes dominant male sterility in rice To clone I Dms1 i , we constructed a near-isogenic line (NIL) I -NJ4 i SP I Dms1 i sp contains the genetic background of the I japonica i rice variety I Ningjing4 i ( I NJ4 i ) but carries a chromosome segment insertion with I Dms1 i introduced from the mutant donor (Figure S1). When using the anther-specific I EAT1 i promoter to drive I OsRIP1 i in I Nip i , the male sterility phenotype mimicking NIL I -Nip i SP I Dms1 i sp appeared (Figure 1g). Keywords: rice; dominant male sterility; ribosome-inactivating protein; translation inhibition EN rice dominant male sterility ribosome-inactivating protein translation inhibition 1932 1934 3 09/20/23 20231001 NES 231001 Rice ( I Oryza sativa i L.) is a major staple food crop feeding more than half of the world human population. [Extracted from the article]

The ability to accurately predict the rheological behavior of the blends of two incompatible polymers is critical to the polymer industry. The constitutive modeling of incompatible polymer blends requires understanding the structure and dynamics of the blends across different length scales. The polydispersity of chain length at the molecular level and nonuniformity of flow field due to dispersed domains at the mesoscopic level present significant challenges to this industrially relevant problem. This work proposes a modeling framework for linear and nonlinear rheology of industrial incompatible polymer blends with sea-island morphology. For the individual components, we adopt the Rolie-Double-Poly model and generate the relaxation spectrum from an optimized molecular weight distribution. We derive a new mixing rule without empirical parameters from the flow field analysis inside and outside the droplets. The phase interface, modeled by an ellipsoidal model, contributes to the apparent rheology only at low shear rates. Our modeling approach is verified by the shear and extensional rheology of eight polymer blends with a broad range of viscosity ratios (0.01–100). We also show that the model has the ability to predict the nonlinear rheological behaviors of incompatible polymer blends with known molecular weight distributions and phase morphology. [ABSTRACT FROM AUTHOR]

Resistance to regulated cell death is one of the hallmarks of human cancers; it maintains cell survival and significantly limits the effectiveness of conventional drug therapy. Leukemia represents a class of hematologic malignancies that is characterized by dysregulation of cell death pathways and treatment-related resistance. As the majority of chemotherapeutic and targeted drugs kill leukemia cells by triggering apoptosis, the observed resistance indicates the need for novel therapeutic strategies to reactivate nonapoptotic cell death programs in refractory leukemia. Necroptosis is a regulated form of necrosis that is precisely modulated by intracellular signaling pathways and thus provides potential molecular targets for rational therapeutic intervention. Indeed, accumulating evidence indicates that many current antitumor agents can activate necroptotic pathways and thereby induce leukemia cell death. Elucidation of the complete regulatory mechanism of necroptosis is expected to accelerate the development of novel therapeutic strategies for overcoming apoptosis resistance in leukemia. Here, we review the latest research advances in the regulatory mechanisms of necroptosis and summarize the progression of necroptosis-based therapeutic strategies in leukemia. [ABSTRACT FROM AUTHOR]

Male sterility in plants provides valuable breeding tools in germplasm innovation and hybrid crop production. However, genetic resources for dominant genic male sterility, which hold great promise to facilitate breeding processes, are extremely rare in natural germplasm. Here we characterized the Sanming Dominant Genic Male Sterility in rice and identified the gene SDGMS using a map-based cloning approach. We found that spontaneous movement of a 1978-bp long terminal repeat (LTR) retrotransposon into the promoter region of the SDGMS gene activates its expression in anther tapetum, which causes abnormal programmed cell death of tapetal cells resulting in dominant male sterility. SDGMS encodes a ribosome inactivating protein showing N-glycosidase activity. The activation of SDGMS triggers transcription reprogramming of genes responsive to biotic stress leading to a hypersensitive response which causes sterility. The results demonstrate that an ectopic gene activation by transposon movement can give birth to a novel trait which enriches phenotypic diversity with practical utility. [ABSTRACT FROM AUTHOR]

Ride-hailing services provide an efficient way to travel, but they also cause some safety incidents, which make female passengers uneasy. Analyzing the safety perceptions of female passengers, particularly their psychological and emotional responses, can assist operators in developing effective solutions and safe travel environments for them. This study explores factors that are likely to affect the safety perception of female ride-hailing passengers using a subjective method (data was obtained from 596 Chinese female passengers). The methodologies adopted mainly include confirmatory factor analysis (CFA) and a maximum-likelihood structural equation model (ML-SEM). A passenger safety perception model is developed by considering various elements such as safety expectation, platform trust, perceived environment, and safety awareness. The results revealed that safety perception is positively influenced by perceived environment and safety expectation (containing three subdimensions, namely, driver behavior, traveling together, and mobile phone dependence). The effects of safety awareness and platform trust on safety perception are mediated by perceived environment and safety expectation, respectively. Regarding overall effects, safety expectation is the most powerful predictor for safety perception of female ride-hailing passengers, followed by platform trust, perceived environment, and safety awareness. Finally, countermeasures are offered from the perspectives of operators, drivers, and passengers to enhance the safety perception of female ride-hailing passengers. A high level of ride-hailing safety would undoubtedly boost the female passenger's trust and consequently ridership. [ABSTRACT FROM AUTHOR]

In this study, a partially bio‐based carbon fiber (CF) precursor is prepared by blending 32 wt% of pyrolytic lignin (PyL) with 68 wt% of poly(acrylonitrile‐co‐itaconic acid) (PANIA), and the effect of PyL on forming conjugated ladder structure during stepwise thermal stabilization is studied. The results of X‐ray photoelectron spectroscopy (XPS) reveal that PyL accelerates the formation of conjugated ladder structure at 230 °C during thermal stabilization for PANIA/PyL, which is 15 °C lower and 13 min earlier than PANIA. The acceleration on forming thermally stable conjugated ladder structure can be confirmed through Fourier‐transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Moreover, the fiber stabilized at 230 °C is subsequently made into PANIA/PyL‐230 CF, which has relatively higher‐ordered graphitic structure and dense morphology without voids. The mechanism of PyL accelerating the formation of conjugated ladder structure during thermal stabilization is discussed. [ABSTRACT FROM AUTHOR]

Background: Exosomes derived from tumor cells (TEXs) are involved in both immune suppression, angiogenesis, metastasis and anticancer stimulatory, but the biological characteristics and role of diffuse large B cell lymphoma (DLBCL)-derived exosomes have been less investigated. Methods: Exosomes (EXOs) were isolated from OCI-LY3, SU-DHL-16, and Raji cells and biological characteristics of EXOs were investigated using electron microscopy, flow cytometry analysis, and Western blot analysis. The protein expression of EXOs was determined by an antibody array. Next, the communication between EXOs and lymphoma cell, stromal cell, dendritic cells (DCs), and T cells was evaluated. Finally, effect of DLBCL TEXs on tumor growth in vivo was investigated. Results: We demonstrated that EXOs derived from DLBCL cell lines displayed malignancy molecules such as c-Myc, Bcl-2, Mcl-1, CD19, and CD20. There was a different protein expression pattern between DLBCL TEXs and Burkitt lymphoma TEXs. DLBCL TEXs were easily captured by DCs and lymphoma cells, and mainly acted as an immunosuppressive mediator, evidenced by induction of apoptosis and upregulation of PD-1 in T cells. Furthermore, the TEXs stimulated not only cell proliferation, migration of stromal cells but also angiogenesis. As a result, the TEXs promoted tumor growth in vivo. On other hand, DLBCL TEXs did not induce apoptosis of DCs. After pulsed with the TEXs, DCs could stimulate clonal expansion of T cells, increase the secretion of IL-6 and TNFα, and decrease the production of immunosuppressive cytokine IL-4 and IL-10. The T cells from tumor bearing mice immunized by TEX were shown to possess superior antilymphoma potency relative to immunization of tumor lysates. Conclusions: This study provides the framework for novel immunotherapies targeting TEXs in DLBCL. [ABSTRACT FROM AUTHOR]