Identification of Tumor Suppressive Genes Regulated by miR-31-5p and miR-31-3p in Head and Neck Squamous Cell Carcinoma

We identified the microRNA (miRNA) expression signature of head and neck squamous cell carcinoma (HNSCC) tissues by RNA sequencing, in which 168 miRNAs were significantly upregulated, including both strands of the miR-31 duplex (miR-31-5p and miR-31-3p). The aims of this study were to identify networks of tumor suppressor genes regulated by miR-31-5p and miR-31-3p in HNSCC cells. Our functional assays showed that inhibition of miR-31-5p and miR-31-3p attenuated cancer cell malignant phenotypes (cell proliferation, migration, and invasion), suggesting that they had oncogenic potential in HNSCC cells. Our in silico analysis revealed 146 genes regulated by miR-31 in HNSCC cells. Among these targets, the low expression of seven genes (miR-31-5p targets: CACNB2 and IL34; miR-31-3p targets: CGNL1, CNTN3, GAS7, HOPX, and PBX1) was closely associated with poor prognosis in HNSCC. According to multivariate Cox regression analyses, the expression levels of five of those genes (CACNB2: p = 0.0189; IL34: p = 0.0425; CGNL1: p = 0.0014; CNTN3: p = 0.0304; and GAS7: p = 0.0412) were independent prognostic factors in patients with HNSCC. Our miRNA signature and miRNA-based approach will provide new insights into the molecular pathogenesis of HNSCC.     

Alloying effects on the hydride formation of Zr(Mn1−xCox)2

To study the alloying effects on ZrMn₂-H system, thermodynamic properties of Zr(Mn_1−xCo_x)₂ hydride were measured by volumetric method. ZrMn₂ gave a single plateau region in the pressure-composition isotherm. On the other hand, double plateaus were clearly observed in Zr(Mn_0.7Co_0.3)₂ and Zr(Mn_0.6Co_0.4)₂-H systems. The appearance of the double plateau characteristics would be explained in view of the hydrogen binding in the tetrahedral occupation sites in Zr(Mn_1−xCo_x)₂. Since the hydrogen binding in the tetrahedral 2ZrMnCo site would be less stable than that in the 2Zr2Mn site, the equilibrium pressure increases with increasing cobalt content. The appearance of the first plateau was ascribed the increase in the bonding of Mn-H in 2Zr2Mn site adjoining the 2ZrMnCo site.     

Electrochemical oxidation of carbon black in concentrated phosphoric acid at 135°C

The electrochemical oxidation of a high surface area carbon black (1000 m²/g) was investigated in 96% H₃PO₄ at 135°C. The total anodic current, the amount of CO₂ evolved and the oxygen content of the carbon were all measured as a function of time and potential. Two anodic processes occurred: the formation of a surface oxide and the evolution of CO₂. Both decreased with time but at different rates so that CO₂ evolution eventually became the major reaction. Various mechanisms to define the corrosion processes are discussed.     

氦对Fe-Cr-Ni合金和Fe-Cr-Mn合金辐照损伤的影响

利用超高压电镜与高能离子加速器连接装置 ,研究了氦 (He)对Fe Cr Ni和Fe Cr Mn两类奥氏体型合金辐照损伤行为的影响。观察了辐照过程中二次点缺陷的演变、空洞的形成以及辐照诱导晶界处溶质元素浓度的变化。实验结果表明 :He能促进两类合金空洞核心的增加 ,但空洞尺寸和密度不同 ;He能有效抑制辐照诱起晶界元素偏析 ,但对不同原子尺寸的溶质原子抑制效果不同。该差别是由于He的注入提高空位移动激活能和改变点缺陷与溶质原子相互作用的效果     

Iron‐Catalyzed Reaction of γ‐Tocopherol with Methyl Linoleate Hydroperoxides in Solutions

γ‐Tocopherol is one of the main constituents in vegetable oils and acts as an antioxidant by trapping lipid‐peroxyl radicals. This study reports reaction products of γ‐tocopherol with lipid‐peroxyl radicals formed by iron‐catalyzed decomposition of methyl linoleate hydroperoxides (MeLOOH) in toluene and methanol solutions. The products in toluene solution were tocored, methyl (8a‐dioxy‐γ‐tocopherone)‐epoxyoctadecenoates (γT‐OO‐epoxyMeL), methyl (8a‐dioxy‐γ‐tocopherone)‐octadecadienoates (γT‐OO‐MeL), γ‐tocopherol biphenyl dimer (γTBD), γ‐tocopherol diphenylether dimer (γTED), and adducts of γ‐tocopherol dimers with the MeLOOH‐derived peroxyl radicals (γTED‐OO‐epoxyMeL, γTBD‐OO‐MeL, and γTED‐OO‐MeL). The iron‐catalyzed reaction in toluene proceeded slowly, whereas the reaction in methanol was relatively fast. The reaction products in methanol were γT‐OO‐epoxyMeL and γTED‐OO‐epoxyMeL together with tocored, γTBD, and γTED. The results indicate that the iron‐catalyzed decomposition of MeLOOH in toluene produces both epoxyperoxyl and peroxyl radicals and that the decomposition in methanol yields only the epoxyperoxyl radicals. These peroxyl radicals could react with the 8a‐carbon‐centered radical of γ‐tocopherol or its dimers.     

Impact of Oncogenic Targets by Tumor-Suppressive miR-139-5p and miR-139-3p Regulation in Head and Neck Squamous Cell Carcinoma

We newly generated an RNA-sequencing-based microRNA (miRNA) expression signature of head and neck squamous cell carcinoma (HNSCC). Analysis of the signature revealed that both strands of some miRNAs, including miR-139-5p (the guide strand) and miR-139-3p (the passenger strand) of miR-139, were downregulated in HNSCC tissues. Analysis of The Cancer Genome Atlas confirmed the low expression levels of miR-139 in HNSCC. Ectopic expression of these miRNAs attenuated the characteristics of cancer cell aggressiveness (e.g., cell proliferation, migration, and invasion). Our in silico analyses revealed a total of 28 putative targets regulated by pre-miR-139 (miR-139-5p and miR-139-3p) in HNSCC cells. Of these, the GNA12 (guanine nucleotide-binding protein subunit alpha-12) and OLR1 (oxidized low-density lipoprotein receptor 1) expression levels were identified as independent factors that predicted patient survival according to multivariate Cox regression analyses (p = 0.0018 and p = 0.0104, respectively). Direct regulation of GNA12 and OLR1 by miR-139-3p in HNSCC cells was confirmed through luciferase reporter assays. Moreover, overexpression of GNA12 and OLR1 was detected in clinical specimens of HNSCC through immunostaining. The involvement of miR-139-3p (the passenger strand) in the oncogenesis of HNSCC is a new concept in cancer biology. Our miRNA-based strategy will increase knowledge on the molecular pathogenesis of HNSCC.     

Organic–inorganic nanomatrix structure and properties of related naturally occurring rubbery macromolecules

The outstanding mechanical properties of soft materials i.e. natural rubber are partly due to the organic–inorganic nanomatrix structure because numerous organic microparticles are dispersed in a small amount of an inorganic nanomatrix composed of inorganic nanoparticles and organic macromolecules. Here we form an organic–inorganic nanomatrix using graft-copolymerization of a vinyl monomer with an inorganic oxide precursor onto natural rubber particles with an average diameter of 1 μm dispersed in water. The inorganic oxide precursor is converted into inorganic oxide nanoparticles through hydrolysis and condensation, forming chemical linkages between natural rubber microparticles and inorganic oxide nanoparticles. Transmission electron microscopy indicates that the organic–inorganic nanomatrix is densely filled with inorganic oxide nanoparticles and the natural rubber microparticles are dispersed in the nanomatrix. This nanomatrix composite realizes both energetic elasticity and entropic elasticity of a soft material, opening a novel field of building block chemistry with respect to a pair of organic microparticles and inorganic nanoparticles.     

Electromigration of sodium ions and electro-osmotic flow in water-saturated, compacted Na-montmorillonite

Sodium ions spiked with ²²Na as a tracer were migrated by electromigration and electro-osmosis in the water-saturated compacted Na-montmorillonite at dry densities 1.0×10³ kg m⁻³, under an electric potential gradient. Dissolved helium was also migrated by electro-osmosis in the montmorillonite. After migration, concentration profiles of the sodium ions and helium were obtained by γ-spectrometry and mass-spectrometric methods, respectively. From the profiles of both chemical species, not only migration due to electrokinetic phenomena but also mechanical dispersion was observed in the montmorillonite. The dispersion coefficients, D_i, and apparent migration rates, U_i^a, of ²²Na and helium were found in the compacted Na-montmorillonite at 1.0×10³ kg m⁻³. The migration of helium in the montmorillonite under an electric potential gradient reflects that of water because helium migrates as an electrically neutral species. The parameters D_He^m, U_He^a, and α_He correspond to those of water. The mechanical dispersion coefficients, D_Na^m, of ²²Na⁺ ions are much smaller than those of water obtained by helium. The dispersivity parameters, α_Na, for ²²Na⁺ obtained from these D_Na and U_Na^a values are 10⁻⁵ m and those for water (α_He) are 10⁻³ m. This indicates that ²²Na⁺ ions migrate in different spaces than water in the compacted montmorillonite under a potential gradient. This finding suggests that the migration of Na⁺ ions occurs in the interlayer and/or on the outer surfaces of the montmorillonite; whereas dissolved helium migrates in the pore water.