Caveolin-1 promotes cancer progression via inhibiting ferroptosis in head and neck squamous cell carcinoma.

BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is an aggressive disease worldwide. Much progress has been made in exploring mechanisms and improving the therapy of HNSCC, but only a few studies have focused on the role of ferroptosis on HNSCC progression. The current study aimed to reveal the underlining mechanisms that caveolin-1 (CAV1)-ROS (reactive oxygen species)-ferroptosis axis affect the process of HNSCC and discover novo therapeutic targets or strategies. METHODS: The role of CAV1 in ferroptosis was analyzed by FerrDb, and its clinical significance was examined by TCGA dataset of HNSCC. The expressions of caveolin-1 (CAV1) in HNSCC tissues were measured by immunohistochemistry, western blot, and real-time PCR assay. Three siRNA sequences were designed to silence CAV1 mRNA in HNSCC cells. Cell proliferation, colony formation, wound-healing, and transwell assays were used to examine the proliferation, migration, and invasion of cancer cells. ROS evaluation and intracellular Fe2+ content assays were performed to examine the levels of ferroptosis. RESULTS: Through the analysis with published data, CAV1 was found to overexpress in HNSCC than normal tissues, and was one of the vital suppressors of ferroptosis pathway. Our study showed that CAV1 was over expressed in HNSCC tissues and the high level of CAV1 predicted poorer prognosis. Further experiments indicated that CAV1 could inhibit the ferroptosis of cancer cells and promote the proliferation, migration and invasion. CONCLUSIONS: Overexpression of CAV1 in HNSCC inhibited the process of ferroptosis, leading to aggressive phenotypes, as well as worse prognosis. The regulatory pathway of CAV1 and ferroptosis are potential targets for designing diagnostic and combined therapeutic strategies for HNSCC patients.

The Au/Ag alloy nanoshuttle-TiO2 nanostructure with enhanced H2 production under visible light and inactivation analysis.

Plasmonic noble metal has been applied in photocatalytic materials, and TiO2 with plasmonic noble metal has been studied for a long time. In this work, we have fabricated incomplete covered Au/Ag alloy nanoshuttle-TiO2 nanomaterials with 268.7 µmol g-1 h-1 H2-evolution in a simple solution method. The considerable photocatalytic performance is mainly due to the enhanced surface plasmon resonance effect of Au/Ag alloy nanoshuttles. It has been found that TiO2 clusters attached to the Au/Ag nanoshuttles surface migrate under electrons irradiation and cover the exposed Au/Ag NS surface to achieve thermodynamic stability, which results in instability of photocatalytic performance. The mechanism has been discussed in detail.

Facile synthesis of graphitic carbon nitride via copolymerization of melamine and TCNQ for photocatalytic hydrogen evolution.

Graphitic carbon nitride (g-C3N4) has been regarded as an intriguing photocatalyst applying to hydrogen generation but suffering rapid recombination of photoinduced electron-hole pairs and insufficient absorption under visible light. We developed a novel one-pot thermal copolymerization method of melamine as a precursor and 7,7,8,8-tetracyanoquinodimethane (TCNQ) as a comonomer to synthesize modified g-C3N4 (abbreviated as X% TCNQ) for the first time, aiming to directly incorporate TCNQ molecular into carbon nitride skeleton for the substitution of low-electronegative carbon for high-electronegative nitride atom. Results revealed that the as-prepared photocatalysts by copolymerization of melamine with TCNQ retained the original framework of g-C3N4, and dramatically altered the electronic and optical properties of carbon nitride. Various measurements confirmed that as-synthesized samples exhibited larger specific surface areas, faster photogenerated charge transfer and broader optical absorption by decreasing the π-deficiency and extending the π-conjugated system, thus facilitating the photocatalytic activity. Specifically, the 0.3% TCNQ exhibited as high as seven times than the pristine g-C3N4 on photocatalytic H2 generation and kept its photoactivity for five circles. This work highlights a feasible approach of chemical protocols for the molecular design to synthesize functional carbon nitride photocatalysts by copolymerizing appropriate g-C3N4 precursor and comonomers.

Enhanced photoresponse of epitaxially grown ZnO by MoO3 surface functionalization.

ZnO has broad applications in optoelectronic devices, including ultraviolet light emitters and photodetectors. Herein we report the impact of MoO3 surface functionalization on the photoresponse of epitaxially grown ZnO. Under illumination with 350 nm UV light, the photocurrent of ZnO is found to be enhanced by 2.87 times after the deposition of 0.2 nm MoO3. As corroborated by in situ ultraviolet photoelectron spectroscopy and X-ray photoelectron spectroscopy results, the enhanced photoresponse derives from MoO3 related gap states within the band gap of ZnO and larger upward band bending at the interface, which is attributed to the strong electron transfer from ZnO to MoO3. Moreover, photoluminescence results reveal that the recombination probability of the photo-generated charge carriers in ZnO is reduced after MoO3 surface functionalization.

Raman determination of carrier concentration in ZnO-based heterostructure light-emitting diodes.

Understanding of the carrier concentration properties of current spreading layers in LED devices is important although difficult to achieve. Here, we present a solution to determine the carrier concentration for current spreading layers in ZnO-based LEDs, based on Raman spectroscopy. Raman spectra and lineshape fitting indicate a hole concentration below 1×1018 cm-3 in the p-type region and an electron concentration of 1.21×1019 cm-3 in n-type. The results from Raman spectroscopy are further qualitatively confirmed by the electroluminescence spectrum and device simulation, which demonstrates its possible application in carrier concentration assessment in multilayered structures.

Photoluminescence enhancement in non-polar ZnO films through metallodielectric mediated Al surface plasmons.

Non-polar ZnO thin films are grown on m-plane sapphire substrates by plasma-assisted molecular beam epitaxy. Emission enhancement from non-polar ZnO thin films coated with Al/AlOx has been studied by photoluminescence spectroscopy. AlOx has been used to mediate the surface plasmon (SP) energy of Al nanoparticles. Taking advantage of the resonant coupling between the UV emission of non-polar ZnO film and Al nanoparticle SPs, an 84-fold enhancement of the UV emission and an 8.3-fold enhancement of internal quantum efficiency (ηint) have been achieved under the optimized sputtering time and energy of SPs.

Enhanced photocatalytic properties of ZnO nanorods by electrostatic self-assembly with reduced graphene oxide.

A series of ZnO nanorod (NR)-reduced graphene oxide (rGO) nanocomposites (NCs) (i.e., ZnO-rGO NCs) with varying rGO loadings were fabricated by electrostatic self-assembly of positively charged ZnO NRs with negatively charged graphene oxide (GO), followed by the hydrothermal reduction of GO to rGO. When compared with bare ZnO NRs, ZnO-5% rGO exhibited significant photoactivity 6 times higher in the photodegradation of rhodamine B (RhB), and 2 times higher than ZnO-5% rGO(H) synthesized by hard integration of GO and ZnO NRs. In the same manner, ZnO-5% rGO exhibited a significant photoactivity 3 times higher in photodegrading phenol, which is 2 times higher than ZnO-5% rGO(H). Furthermore, the adsorption properties of ZnO-rGO NCs towards RhB and phenol were significantly different as a result of the opposite charges of the two pollutants in aqueous solution, which also led to the formation of different key free radicals during the degradation reaction. Based on various characterization techniques, it is concluded that the enhanced photoactivity and photostability of ZnO-5% rGO originated from the synergistic effects between ZnO NRs and rGO nanosheets including higher specific surface area, enhanced photogenerated carrier separation, and strengthened protection effects from intimate rGO coupling. However, these synergistic effects were weaker in ZnO-5% rGO(H) which reflects the key importance of surface charge modification in producing a well-contacted interface.

The Rb2 31Π g state: Observation and analysis.

This paper reports observations and analysis of the Rb2 31Π g state. A total of 323 rovibrational term values spanning the range of the rotational quantum number J = 7 through 77 and the vibrational quantum number v = 2 through 23 (about 1/3 of the potential well depth) were measured using the optical-optical double resonance technique. The term values are simulated within a model of a piece-wise multi-parameter potential energy function based on the generalized splines. This function not only enables a reproduction of the experimental data with a reasonable quality but also approximates the available ab initio function in its whole range with a uniform accuracy.

Great photoluminescence enhancement in Al-sputtered Zn0.78Mg0.22O films.

Zn0.78Mg0.22O thin films were grown on a-plane sapphire substrates by plasma-assisted molecular beam epitaxy. Compared with ZnO, the crystal quality of Zn0.78Mg0.22O thin films degrades significantly, which results in low internal quantum efficiency (ηint). Besides improving the quality of Zn0.78Mg0.22O, an effective method has been used to enhance the internal quantum efficiency and the UV emission of Zn0.78Mg0.22O by sputtering Al nanoparticles. Taking advantage of the resonant coupling between UV emission of Zn0.78Mg0.22O film and Al nanoparticle surface plasmons (SPs), a 59-fold enhancement of the UV emission and a 3.5-fold enhancement of ηint has been achieved under the optimized sputtering time. Moreover, the enhancement ratio is stable after two months. It paves a facile way in fabricating high-efficiency UV optoelectronic devices.

Measurement of the Na2 51Σg+→A1Σu+ and 61Σg+→A1Σu+ transition dipole moments using optical-optical double resonance and Autler-Townes spectroscopy.

Accurate knowledge of transition dipole moment matrix elements is crucial since important parameters associated with the interaction of light with matter, such as emission and absorption line intensities, lifetimes, and Einstein coefficients, depend on these matrix elements. We report here an experimental study of the Na2 51Σg+↔A1Σu+ and 61Σg+↔A1Σu+ electronic transition dipole moments and their dependence on internuclear distance. We have measured absolute transition dipole matrix elements for ro-vibrational transitions of the Na2 51Σg+↔A1Σu+ and 61Σg+↔A1Σu+ electronic transitions using Autler-Townes and optical-optical double resonance spectroscopy, and we compare the results to ab initio theoretical values [A. Sanli et al., J. Chem. Phys. 143, 104304 (2015)].

Enhanced internal quantum efficiency in non-polar ZnO/Zn0.81Mg0.19O multiple quantum wells by Pt surface plasmons coupling.

Non-polar-oriented ZnO/Zn0.81Mg0.19O multiple quantum wells (MQWs) were grown on r-plane sapphire substrates by plasma-assisted molecular beam epitaxy. The internal quantum efficiency (η(int)) of the non-polar MQWs was only 1.8%. The degraded quality of non-polar MQWs is the main factor for the low η(int). Besides improving the quality of non-polar MQWs, an effective way to enhance the UV emission of the non-polar MQWs by sputtering Pt nanoparticles has been used. Employing the resonant coupling between UV emission from the MQWs and Pt nanoparticle surface plasmons (SPs), a 20-fold enhancement of the UV emission has been achieved under the optimized sputtering time. Moreover, the η(int) value of the non-polar MQWs has been strongly improved with the help of Pt. 6.7-fold enhancement of η(int) has been achieved due to SPs coupling. It paves a new way in designing highly efficient non-polar LEDs.

Enhanced photoluminescence of nonpolar p-type ZnO film by surface plasmon resonance and electron transfer.

Nonpolar oriented Na-doped ZnO films were grown on m-plane sapphire substrates by plasma-assisted molecular beam epitaxy. The films show repeatable p-type conductivity with a hole concentration of about 3.0×10(16) cm(-3) as identified by the Hall-effect measurements. 10-fold enhancement in the near-band-edge (NBE) emission of the nonpolar p-type ZnO by employing Pt nanoparticle surface plasmons has been observed. In addition, the deep level emission has been entirely suppressed. The underlying mechanism behind the enhancement of NBE emission and the quenching of defect emission is a combination of the electron transfer and the resonant coupling between NBE emission and Pt nanoparticle surface plasmons.

60-fold photoluminescence enhancement in Pt nanoparticle-coated ZnO films: role of surface plasmon coupling and conversion of non-radiative recombination.

Giant 60-fold enhanced ultraviolet (UV) emission is obtained in Pt nanoparticle-assembled ZnO film. Besides surface plasmons coupling, the conversion of non-radiative recombination into UV emission makes great contributions to the enhancement. It paves a new way in designing high-efficiency UV optoelectronic devices without defect-related energy loss.

Theoretical Understanding of Electromigration-Related Surface Diffusion and Current-Induced Force in Ag-Pd Systems.

Electromigration, as a common reason for interconnect failure, is becoming increasingly important in the ongoing decrease in the integrated circuit manufacturing process. A study is being carried out utilizing the ab initio calculational method to gain a deeper understanding of electromigration, with a focus on the atom diffusion process in the Ag-Pd alloy system, a commonly used interconnect material. We begin by establishing that the primary mechanism of diffusion is step-edge diffusion on the (111) surface. Following this, we examine the current-induced force exerted on the migrating Ag atom. The Pd substitutional defect reveals an effect that increases the energy barrier of diffusion and decreases the current-induced force that powers the directional migration.

A Reconfigurable All-Optical-Controlled Synaptic Device for Neuromorphic Computing Applications.

Retina-inspired visual sensors play a crucial role in the realization of neuromorphic visual systems. Nevertheless, significant obstacles persist in the pursuit of achieving bidirectional synaptic behavior and attaining high performance in the context of photostimulation. In this study, we propose a reconfigurable all-optical controlled synaptic device based on the IGZO/SnO/SnS heterostructure, which integrates sensing, storage and processing functions. Relying on the simple heterojunction stack structure and the role of energy band engineering, synaptic excitatory and inhibitory behaviors can be observed under the light stimulation of ultraviolet (266 nm) and visible light (405, 520 and 658 nm) without additional voltage modulation. In particular, junction field-effect transistors based on the IGZO/SnO/SnS heterostructure were fabricated to elucidate the underlying bidirectional photoresponse mechanism. In addition to optical signal processing, an artificial neural network simulator based on the optoelectrical synapse was trained and recognized handwritten numerals with a recognition rate of 91%. Furthermore, we prepared an 8 × 8 optoelectrical synaptic array and successfully demonstrated the process of perception and memory for image recognition in the human brain, as well as simulated the situation of damage to the retina by ultraviolet light. This work provides an effective strategy for the development of high-performance all-optical controlled optoelectronic synapses and a practical approach to the design of multifunctional artificial neural vision systems.

IL-1α facilitates GSH synthesis to counteract oxidative stress in oral squamous cell carcinoma under glucose-deprivation.

Understanding the intrinsic mechanisms underpinning cancer metabolism and therapeutic resistance is of central importance for effective nutrition-starvation therapies. Here, we report that Interleukin 1A (IL1A) mRNA and IL-1α protein facilitate glutathione (GSH) synthesis to counteract oxidative stress and resistance against nutrition-starvation therapy in oral squamous cell carcinoma (OSCC). The expression of IL1A mRNA was elevated in the case of OSCC associated with unfavorable clinical outcomes. Both IL1A mRNA and IL-1α protein expression were increased under glucose-deprivation in vitro and in vivo. The transcription of IL1A mRNA was regulated in an NRF2-dependent manner in OSCC cell lines under glucose-deprivation. Moreover, the IL-1α conferred resistance to oxidative stress via GSH synthesis in OSCC cell lines. The intratumoral administration of siRNAs against IL1A mRNA markedly reversed GSH production and sensitized OSCC cells to Anlotinib in HN6 xenograft models. Overall, the current study demonstrates novel evidence that the autocrine IL-1α favors endogenous anti-oxidative process and confers therapeutic resistance to nutrition-starvation in OSCCs.

Engraftment of heavily transfused patients with severe aplastic anemia with a fludarabine-based regimen.

We have developed a practical conditioning regimen without anti-thymocyte globulin (ATG), irradiation, or other myeloablative alkylating agent for low-income countries in which patients with severe aplastic anemia (SAA), who usually have heavily transfused and a prolonged disease history. The application of ATG, Busulphan, and/or irradiation to cyclophosphamide (Cy) to avoid graft rejection has many short- and long-term complications. In this study, we focused on evaluating a fludarabine-based conditioning regimen, among 83 patients with SAA. Patients were treated with fludarabine (40 mg/m(2) /d; day [-5 to -2]) and cyclophosphamide (50 mg/kg/d; day [-5 to -2]). Altogether, 81 patients indicated initial engraftment, whereas two cases showed primary graft failure. And four of the 81 cases indicated graft rejection during follow-up. Regardless of a high cumulative incidence of acute (55/83; 66.2% grade II-IV; 47/83; 56.6% III-IV) and chronic graft-versus-host disease (50/83; 60.2%), in total, 77 patients showed durable engraftment and transfusion independence, and 64 are alive at a median time of 49 months with an overall survival rate of 66%. In conclusion, this conditioning indicated well toleration, mild toxicity, durable engraftment, excellent survival as well as less cost. Its application might shed new light on SAA at high risk of graft rejection in resource-limited countries.

Discovery and excavation of lichen bioactive natural products.

Lichen natural products are a tremendous source of new bioactive chemical entities for drug discovery. The ability to survive in harsh conditions can be directly correlated with the production of some unique lichen metabolites. Despite the potential applications, these unique metabolites have been underutilized by pharmaceutical and agrochemical industries due to their slow growth, low biomass availability, and technical challenges involved in their artificial cultivation. At the same time, DNA sequence data have revealed that the number of encoded biosynthetic gene clusters in a lichen is much higher than in natural products, and the majority of them are silent or poorly expressed. To meet these challenges, the one strain many compounds (OSMAC) strategy, as a comprehensive and powerful tool, has been developed to stimulate the activation of silent or cryptic biosynthetic gene clusters and exploit interesting lichen compounds for industrial applications. Furthermore, the development of molecular network techniques, modern bioinformatics, and genetic tools is opening up a new opportunity for the mining, modification, and production of lichen metabolites, rather than merely using traditional separation and purification techniques to obtain small amounts of chemical compounds. Heterologous expressed lichen-derived biosynthetic gene clusters in a cultivatable host offer a promising means for a sustainable supply of specialized metabolites. In this review, we summarized the known lichen bioactive metabolites and highlighted the application of OSMAC, molecular network, and genome mining-based strategies in lichen-forming fungi for the discovery of new cryptic lichen compounds.

Self-Powered Flexible Ultraviolet Photodetectors Based on CuI/a-ZTO Heterojunction Processed at Room Temperature.

For traditional wide-bandgap semiconductor materials, a high-temperature process is unavoidable for improving crystallization quality, so the substrate of the device is greatly limited. In this work, zinc-tin oxide (a-ZTO) amorphous oxide processed by the pulsed laser deposition method was utilized as the n-type layer, which exhibits considerable electron mobility and optical transparency, and can be deposited at room temperature. At the same time, by combining p-type CuI grown by the thermal evaporation method, a vertically structured ultraviolet photodetector based on CuI/ZTO heterojunction was obtained. The detector demonstrates self-powered properties, with an on-off ratio exceeding 104, and rapid response with a rise time of 2.36 ms and a fall time of 1.49 ms. Also, the photodetector shows long-term stability with 92% retention after 5000 s cyclic lighting and maintains reproducible response in frequency dependence measurement. Furthermore, the flexible photodetector on poly(ethylene terephthalate) (PET) substrates was constructed, exhibiting fast response and durability in the bending state. This is the first time that the heterostructure based on CuI has been applied in the flexible photodetector. The excellent results indicate that the combination of amorphous oxide and CuI has the potential for ultraviolet photodetectors, and will broaden the application range of high-performance flexible/transparent optoelectronic devices in the future.

Lanostane triterpenoids from mycelia-associated Ganoderma sinense and their anti-inflammatory activity.

Seven previously undescribed lanostane triterpenoids, ganoderic acid M1 (1), M2 (2), M3 (3), M4 (4), M5 (5), M6 (6), and M7 (7), together with eight known compounds, were isolated from mycelia of the basidiomycete Ganoderma sinense (Ganodermataceae). The structures of all compounds were elucidated by spectroscopic analysis. The possible biosynthetic pathway of these fifteen triterpenoids was proposed. Some of the compounds were evaluated for their anti-inflammatory activity by measuring the production of nitric oxide (NO), TNF-α, and IL-6 in RAW264.7 macrophage cells induced by lipopolysaccharide. Lanosta-7,9(11),24-trien-3ß,15α,22ß-triacetoxy-26-oic acid (14) exhibited the strongest inhibition of NO production with an IC50 of 0.6 ± 0.1 µM and completely inhibited the secretion of TNF-α and IL-6 at 10 µM. The structure-activity relationship of the anti-inflammatory activity is discussed.