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Long noncoding RNAs (lncRNAs) have emerged as new regulatory molecules implicated in diverse biological processes, including therapeutic resistance. However, the mechanisms underlying lncRNA-mediated temozolomide (TMZ) resistance in glioblastoma (GBM) remain largely unknown. To illustrate the role of lncRNA in TMZ resistance, we induce TMZ-resistant GBM cells, perform a lncRNA microarray of the parental and TMZ-resistant cells, and find an unreported lncRNA in GBM, lnc-TALC (temozolomide-associated lncRNA in glioblastoma recurrence), correlated with TMZ resistance via competitively binding miR-20b-3p to facilitate c-Met expression. A phosphorylated AKT/FOXO3 axis regulated lnc-TALC expression in TMZ-resistant GBM cells. Furthermore, lnc-TALC increased MGMT expression by mediating the acetylation of H3K9, H3K27 and H3K36 in MGMT promoter regions through the c-Met/Stat3/p300 axis. In clinical patients, lnc-TALC is required for TMZ resistance and GBM recurrence. Our results reveal that lnc-TALC in GBM could serve as a therapeutic target to overcome TMZ resistance, enhancing the clinical benefits of TMZ chemotherapy. Temozolomide resistance in glioblastoma is associated with MGMT overexpression. Here, the authors identify a lncRNA that is a competitive endogenous RNA for miR-20b-3p, which causes c-Met activation to modulate acetylation of histone H3 on MGMT promoter through Stat3/p300 complex to increase MGMT expression and temozolomide resistance.

Activation of receptor tyrosine kinase (RTK) protein is frequently observed in malignant progression of gliomas. In this study, the crosstalk activation of epidermal growth factor receptor (EGFR) and mesenchymal-epithelial transition factor (MET) signaling pathways is demonstrated to contribute to temozolomide (TMZ) resistance, resulting in an unfavorable prognosis for patients with glioblastoma. To simultaneously mitigate EGFR and MET activation, a dual functionalized brain-targeting nanoinhibitor, BIP-MPC-NP, is developed by conjugating Inherbin3 and cMBP on the surface of NHS-PEG 8 -Mal modified MPC-nanoparticles. In the presence of BIP-MPC-NP, DNA damage repair is attenuated and TMZ sensitivity is enhanced via the down-regulation of E2F1 mediated by TTP in TMZ resistant glioma. In vivo magnetic resonance imaging (MRI) shows a significant repression in tumor growth and a prolonged survival of mice after injection of the BIP-MPC-NP and TMZ. These results demonstrate the promise of this nanoinhibitor as a feasible strategy overcoming TMZ resistance in glioma. Receptor tyrosine kinases are often activated in malignant gliomas. Here, the authors develop a dual functionalized brain targeting nano-inhibitor to simultaneously target EGFR and MET pathways, and show this can overcome temozolomide resistance in glioma.

Oily sludge is a complex emulsified waste consisting of water, oil, and solid particles. Conventional treatments are often inefficient, energy-intensive, and prone to causing secondary pollution. This study proposes a green demulsification technology based on ozone micro–nanobubbles (O3MNBs) by constructing an experimental system to analyze its effects and mechanisms of action on oily sludge treatment. The O3MNBs exhibited a mean particle size of 831 nm and generated a substantial amount of hydroxyl radicals (·OH, 250.4 μmol·L−1) in situ. Compared with conventional aeration, the dissolved ozone concentration and residence time in water of O3MNBs increased by 192% and 213%, respectively. During bubble collapse, intense pressure waves and high-speed microjets were generated to disrupt sludge aggregates, promoting the dispersion of sludge particles while simultaneously stripping oil films. Thus, the oil removal rate reached 41.5%, demonstrating the high demulsification efficiency of O3MNBs. Furthermore, ozone and ·OH attacked alkane C-H bonds in the oil phase, oxidizing hydrophobic films into hydrophilic products and decomposing surfactants that stabilize emulsions. This process promoted oil droplet coalescence and degradation into small organic molecules. After O3MNB treatment, the absorption peak of alkane C-H bonds gradually reduced, while a new C=O absorption peak appeared. This study provides a theoretical foundation and technical support for environmentally sustainable treatment of oily sludge by O3MNB application, offering an effective alternative to chemical demulsification without secondary pollution.

Food safety has recently attracted increasing attention, underscoring the need for timely and accurate on-site testing technologies. Optical detection, among various methods, offers notable advantages, including ease of use and rapid results, making it a promising approach for food safety applications. This paper reviews the fundamental principles of optical inspection for food field examination and explores its practical applications, including techniques such as surface-enhanced Raman scattering, UV–visible absorption spectroscopy, and fluorescence detection. Furthermore, this review discusses the integration of detection technologies with nanotechnology and smartphone-based systems. In addition, this review discusses the current applications, challenges, and potential solutions associated with optical detection in on-site food inspections.

Neutrophil extracellular traps (NETs) produced by tumor-infiltrating neutrophils (TINs) are associated with poor prognosis in patients with several types of cancer. However, the mechanisms underlying the involvement of NETs in glioma progression remain largely unknown. This study aimed to elucidate the roles of NETs in biological processes that drive the crosstalk between glioma progression and the tumor microenvironment. Neutrophil infiltration and NETs formation were investigated in glioma tissue through immunohistochemistry, and their relationships with clinicopathological features and outcomes were statistically evaluated. The effects of NETs on glioma cell progression were studied in a co-culture system. and experiments validated the reactive oxygen species activity and cytokine production of TINs, as well as the ERK signaling pathway activation and the metastasis of gliomas. Neutrophil infiltration and NETs formation were induced in high-grade glioma compared with low-grade glioma. NETs induced by TINs were determined to be an oncogenic marker of high-grade gliomas and to be involved in cell proliferation and invasion. NETs overproduction promoted glioma cell proliferation, migration, and invasion. Furthermore, HMGB1 was found to bind to RAGE and activate the NF-κB signaling pathway . In addition, NETs stimulated the NF-κB signaling pathway, thus promoting IL-8 secretion in glioblastoma. Subsequently, IL-8 recruited neutrophils which in turn mediated NETs formation the PI3K/AKT/ROS axis in TINs. Our results suggest that NETs produced by TINs mediate the crosstalk between glioma progression and the tumor microenvironment by regulating the HMGB1/RAGE/IL-8 axis. Targeting NETs formation or IL-8 secretion may be an effective approach to inhibit glioma progression.

TTFields is a novel treating modality of glioblastoma (GBM) which can significantly prolong the overall survival (OS) of newly diagnosed or recurrent glioblastoma. Some researchers have revealed that a variety of factors can affect the efficacy of TTFields. So, we review the available literature about the influencing factors on efficacy of TTFields and then choose two experimentally supported factors: the dose of dexamethasone and compliance of TTFields to perform a meta-analysis. The PubMed, Embase, and the Cochrane Library are searched. Five articles are identified between 2014 and 2017. Three articles are about the compliance of TTFields. Two articles are about the dose of dexamethasone. The Newcastle-Ottawa Quality Assessment Scale (NOS) is used as an assessment tool to evaluate the methodological quality of all included trials. The scale’s range varies from 0 to 9 stars. According to the Cochrane Handbook for Systematic Reviews of Interventions, articles are graded in six items to evaluate the risk of bias. Two reviewers rate the studies independently and the final decision is reached by consensus. Our data shows that the median OS is conspicuously longer in the TTFields group in which the dose of dexamethasone is ≤ 4.1 mg, WMD = 9.23 [95% CI 5.69–12.78]; P < 0.05). And the patients whose compliance of TTFields treatment ≥ 75% (≥ 18 h per day) have a significant lower overall survival risk than the patients whose compliance of TTFields treatment < 75% (HR = 0.57 [95% CI 0.46–0.70]; P < 0.00001).TTFields is a safe and efficient novel treatment modality. The dose of dexamethasone ≤ 4.1 mg of TTFields treatment and the compliance of TTFields treatment ≥ 75%, ≥ 18 h per day are beneficial to the prognosis of the glioblastoma patients.

A brain organoid is a self-organizing three-dimensional tissue derived from human embryonic stem cells or pluripotent stem cells and is able to simulate the architecture and functionality of the human brain. Brain organoid generation methods are abundant and continue to improve, and now, an in vivo vascularized brain organoid has been encouragingly reported. The combination of brain organoids with immune-staining and single-cell sequencing technology facilitates our understanding of brain organoids, including the structural organization and the diversity of cell types. Recent publications have reported that brain organoids can mimic the dynamic spatiotemporal process of early brain development, model various human brain disorders, and serve as an effective preclinical platform to test and guide personalized treatment. In this review, we introduce the current state of brain organoid differentiation strategies, summarize current progress and applications in the medical domain, and discuss the challenges and prospects of this promising technology.

Silicone rubber, primarily composed of polydimethylsiloxane (PDMS) chains, is widely used in sealing materials due to its excellent flexibility and durability. Its performance is significantly affected by environmental conditions, with humid-heat aging being a major factor of degradation. In this study, molecular dynamics simulations were conducted to systematically investigate the effects of water and temperature on PDMS at the molecular scale. The glass transition temperature (Tg) and free volume distribution were analyzed to evaluate the mobility of polymer chains under hydrated conditions. Mechanical simulations (including tensile and compressive deformation) indicate that the combined effect of elevated temperature and moisture significantly accelerates the degradation of rubber properties. Thermal decomposition simulations indicate that, under high-temperature and humid conditions, PDMS main chains gradually break into small molecules, with free radical reactions further promoting the aging process. The results elucidate the molecular mechanisms underlying silicone rubber performance deterioration under the coupled action of water and temperature, providing a theoretical basis for service-life prediction and durability design of sealing materials.

Spinal cord injury (SCI) is a devastating condition characterized by a complex cascade of secondary injury following an initial mechanical insult. Among the mechanisms of secondary injury, multiple forms of programmed cell death (PCD)—including apoptosis, necroptosis, and pyroptosis—play key roles in tissue degeneration and loss of function. PANoptosis is a recently proposed concept of cell death that integrates the aforementioned three pro-inflammatory PCD pathways into a single process via a multi-protein complex called the PANoptosome. This review summarizes evidence for the involvement of PANoptosis in SCI pathophysiology and discusses intervention strategies targeting PANoptosis. Targeting PANoptosis offers a novel, holistic approach to mitigating secondary injury in SCI. However, its clinical translation remains challenging and requires further studies to validate efficacy and safety. Elucidating the assembly mechanisms of the PANoptosome and identifying critical regulatory molecules will aid in developing combination therapies and biomarkers to improve neuronal survival and functional recovery in patients with SCI.

Lithium (Li) metal is regarded as the ultimate anode for next‐generation Li‐ion batteries due to its highest specific capacity and lowest electrochemical potential. However, the Li metal anode has limitations, including virtually infinite volume change, nonuniform Li deposition, and an unstable electrode–electrolyte interface, which lead to rapid capacity degradation and poor cycling stability, significantly hindering its practical application. To address these issues, intensive efforts have been devoted toward accommodating and guiding Li deposition as well as stabilizing the interface using various carbon materials, which have demonstrated excellent effectiveness, benefiting from their vast variety and excellent tunability of the structure–property relationship. This review is intended as a guide through the fundamental challenges of Li metal anodes to the corresponding solutions utilizing carbon materials. The specific functionalities and mechanisms of carbon materials for stabilizing Li metal anodes in these solutions are discussed in detail. Apart from the stabilization of the Li metal anode in liquid electrolytes, attention has also been paid to the review of anode‐free Li metal batteries and solid‐state batteries enabled by strategies based on carbon materials. Furthermore, we have reviewed the unresolved challenges and presented our outlook on the implementation of carbon materials for stabilizing Li metal anodes in practical applications. This article reviews the fundamental challenges of Li metal anodes and the respective solutions utilizing carbon materials based on their specific functionalities. It also provides a critical review of the limitations and the remaining challenges of these approaches and presents an outlook into the development of carbon materials for future Li metal batteries. Apart from batteries with liquid electrolytes, this review also pays particular attention to anode‐free and solid‐state Li metal batteries.