Publications by authors named "Shuangyan Lin"

The rational construction of highly efficient electrocatalysts for the oxygen evolution reaction (OER) plays a critical role in energy conversion systems. Designing heterostructures is a common and effective strategy to improve the performance of electrocatalysts. In this paper, an MnS/CoS/NiS heterostructure was synthesized on Ni foam using a one-step vulcanization method.

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Triple-negative breast cancer (TNBC) is a subtype of breast cancer with a poor prognosis. Cancer-associated fibroblasts (CAFs) play a critical role in regulating TNBC tumor development. This study aimed to identify and characterize a specific subtype of CAFs associated with TNBC.

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Background: Total pelvic exenteration is the ultimate solution for rectovesicovaginal fistula caused by radiation therapy, yet total pelvic exenteration frequently causes intraoperative complications and postoperative complications. These complications are responsible for the dysfunction of lower extremities, impaired quality of life, and even the high long-term morbidity rate, thus multidisciplinary cooperation and early intervention for prevention of complications are necessary. Physical therapy was found to reduce the postoperative complications and promote rehabilitation, yet the effect on how physiotherapy prevents and treats complications after total pelvic exenteration and pelvic lymphadenectomy remains unclear.

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Background: Triple-negative breast cancer (TNBC) is an aggressive cancer that affects about 13/100,000 women yearly. Patients with TNBC are often resistant to endocrine and molecular targeted therapy, making clinical treatment challenging. Researches indicate that tumor microenvironment (TME) is related to prognosis in many cancers.

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Background: Tumor immune microenvironment (TIME) is crucial for tumor initiation, progression, and metastasis; however, its relationship with lung adenocarcinoma (LUAD) is unknown. Traditional predictive models screen for biomarkers that are too general and infrequently associated with immune genes.

Methods: RNA sequencing data of LUAD patients and immune-related gene sets were retrieved from public databases.

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Transition metal sulfides (TMSs) are considered as one of the promising electrode materials due to their fascinating redox reversibility and electronic conductivity. However, volume expansion during the charge/discharge process impedes their practical applications. The reasonable design of TMS electrode materials with unique morphology can improve the energy storage performance.

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It is important to develop highly efficient and durable Earth-abundant oxygen evolution reaction (OER) electrocatalysts by an energy- and time-saving strategy. Herein, a facile strategy was used to synthesize S-doped nickel-iron oxyhydroxide (S-Ni/FeOOH) nanoparticles on nickel-iron foam (NFF) (S-Ni/FeOOH@NFF), which exhibits a striking enhancement of OER performance compared to Ni/FeOOH@NFF. The free-standing S-Ni/FeOOH@NFF electrode possesses a low overpotential of 229 mV at a current density of 10 mA cm, which is 180 mV lower than that of Ni/FeOOH@NFF.

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Constructing a heterostructure is an efficient strategy to enhance the catalytic activity toward the oxygen evolution reaction (OER). Herein, Ce-modified Ni(OH) nanoparticles are anchored on Ni-MOF nanosheets by the electrodeposition strategy, forming a self-supporting electrode of Ce-m-Ni(OH)@Ni-MOF. The Raman spectrum proves that both Ce(OH) and Ce doping exist in Ce-modified Ni(OH) nanoparticles.

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2D bimetal metal organic frameworks (MOFs) are recognized as one of the most promising electrocatalysts for the oxygen evolution reaction (OER). Herein, a facile approach was proposed to construct NiFe-MOF nanosheets on Fe foam (FF). As a self-supporting electrode, the NiFe-MOF/FF electrode shows impressive electrocatalytic OER performance.

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Rational design and controllable synthesis of metal-organic frameworks nanosheets is critical for electrochemical catalysis. Herein, a carnation-like ZIF-9 nanostructure made of nanosheets is grown on nickel foam (ZIF-9/NF) by a simple one-step solvothermal method, the morphology evolution and the electrocatalytic oxygen evolution properties have been investigated by controlling the solvothermal time. The binder-free ZIF-9-d/NF (60 h, solvothermal time is 60 h) electrode delivers efficient electrocatalytic oxygen evolution reaction activity with low overpotentials of 312 and 337 mV at 50 and 100 mA cm, respectively.

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The function of centromere protein U () gene in breast cancer has not been well understood. Therefore, we explored the expression profiles of gene in breast carcinoma to better understand the functions of this gene, as well as the relationship between expression and the prognosis of breast carcinoma patients. Our results indicate that was expressed at significantly higher levels in cancerous tissues than in normal tissues.

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Background: Sperm-associated antigen 1 (SPAG1) has been identified as a marker of pancreatic cancer progression and promoter of cell motility; however, its role in breast cancer is not completely understood.

Methods: SPAG1 expression in breast cancer tissues and normal tissues was obtained from online databases. Knockdown function assays were designed and conducted to verify the functional role of SPAG1 in breast cancer cell lines.

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Robust and economical catalysts are imperative to realize the versatile applications of hydrogen. Herein, a 1T-MoS/N-doped NiSe composite was rationally synthesized a solvothermal method, in which the MoS nanosheets have a stable 1T phase structure, and the NiSe nanoparticles serve as a cocatalytic support for MoS. The nonnegligible electronic couplings between NiSe and MoS could facilitate the optimization of their electronic structure and then improve the hydrogen adsorption.

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Vulnerable atherosclerotic (AS) plaque is the major cause of cardiovascular death. However, clinical methods cannot directly identify the vulnerable AS plaque at molecule level. Herein, osteopontin antibody (OPN Ab) and NIR fluorescence molecules of ICG co-assembled Ti C nanosheets are reported as an advanced nanoprobe (OPN Ab/Ti C /ICG) with enhanced photoacoustic (PA) performance for direct and non-invasive in vivo visual imaging of vulnerable AS plaque.

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The development of Li-S batteries is largely impeded by the growth of Li dendrites and polysulfide shuttling. To solve these two problems simultaneously, herein the study reports a "single atom array mimic" on ultrathin metal organic framework (MOF) nanosheet-based bifunctional separator for achieving the highly safe and long life Li-S batteries. In the designed separator, the periodically arranged cobalt atoms coordinated with oxygen atoms (CoO moieties) exposed on the surface of ultrathin MOF nanosheets, "single atom array mimic", can greatly homogenize Li ion flux through the strong Li ion adsorption with O atoms at the interface between anode and separator, leading to stable Li striping/plating.

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Centromere protein U (CENPU) is a novel transcriptional repressor that is associated with different types of cancer. However, its function in breast cancer is poorly understood. In the present study, it was identified that CENPU was highly expressed in breast cancer tissues compared with expression in normal breast tissues (P=0.

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Objective: Lung cancer, which is the leading cause of cancer death worldwide, is influenced by a wide variety of environmental and genetic risk factors. The silent information regulator 1 () gene is located on the long arm of chromosome 10 (10q21.3) and has been shown to play crucial roles in lung cancer development in previous studies.

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Background And Aims: Matrix metalloproteinase-9 (MMP-9) -1562 C/T gene polymorphism has been identified as a susceptible gene for multiple autoimmune diseases (ADs), but studies are inconsistent. The aim of this study was to assess the overall association between MMP-9 gene polymorphism and multiple ADs using a meta-analysis.

Methods: Databases of Pubmed, Embase and Web of Science updated to March 1, 2016 were retrieved.

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Three μ-O bridged Dy squares, {[Dy(μ-O)(HL)(HO)](NO)(OH)}·2HO·2CHOH (1), [Dy(μ-O)(HL)(SCN)]·2HO·4CHOH (2) and [Dy(μ-O)(HL)(SCN)]·6HO (3) were assembled by using a Schiff base ligand and its dimerized and reduced congener, respectively. These complexes share a similar μ-O bridged Dy core, while, both the coordination geometry and metal-ligand interactions are slightly changed upon the modulation of the ligands, resulting in distinct single-molecular magnetic (SMM) and single-molecular toroic (SMT) properties. In complex 1, the Schiff base ligands are in an antiparallel fashion and all Dy ions are in a similar coordination geometry, realizing the toroidal arrangement of magnetic moments.

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The roles of Silent mating type information regulation 2 homolog 1 (SIRT1) and High mobility group A1 (HMGA1) in human diseases have been extensively studied separately; however, to the best of our knowledge, the current study is the first to report on their interrelationship in lung cancer. The association of SIRT1 and HMGA1 in non-small cell lung cancer (NSCLC) was investigated by evaluating their expression and prognostic significance in 260 patients with NSCLC using immunohistochemistry. SIRT1 and HMGA1 expression were found to be significantly correlated with each other (P<0.

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The synthesis, structural characterization, and magnetic properties of four related heterometallic complexes with formulas [Dy(III)2Co(II)(C7H5O2)8]·6H2O (1), [Dy(III)2Ni(II)(C7H5O2)8]·(C7H6O2)2 (2), Tb(III)2Co(II)(C7H5O2)8 (3), and Dy(III)2Cd(II)(C7H5O2)8 (4) were reported. Each of complexes has a perfectly linear arrangement of the metal ions with two terminal Ln(III) (Ln(III) = Dy(III), Tb(III)) ions and one central M(II) (M(II) = Co(II), Ni(II), Cd(II)) ion. It was found that 1-3 displayed obvious magnetic interactions between the spin carriers according to the direct current (dc) susceptibility measurements.

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A series of one dimensional chain complexes [Ln(hfac)3]2·[Cu(hfac)2]2·4(3pyvd)·n-C7H16 (Ln = Gd(1), Tb(2), Dy(3)) containing 2p, 3d and 4f spin carriers have been successfully synthesized and magnetically characterized where the verdazyl radicals represent the bridge linking copper(II) and lanthanide(III) ions. Rough estimation of magnetic behaviors of complex 1 revealed that the coupling between a Gd(III) ion and a radical is weakly ferromagnetic, while alternating-current susceptibilities of complexes 2 and 3 suggest no slow magnetic relaxations exist at low temperature.

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The initial employment of a triketone ligand in 4f coordination chemistry afforded a series of dinuclear complexes. Magnetic studies revealed that an antiferromagnetic interaction exists in a digadolinium(III) compound, while a dysprosium(III) constructed complex exhibits single-molecule magnet (SMM) behaviour at low temperatures with an energy barrier of 86.8 K.

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The reaction of Mn(OAc)2·4H2O and Ln(NO3)3·6H2O with N-(2-aminopropyl)-2-hydroxybenzamide and salicylic aldehyde in methanol/methylene dichloride produces yellow crystals of Ln2Mn(C7H5O2)8 (Ln = Gd (), Tb (), Dy (), Ho () and Er ()), in the presence of triethylamine. Three metal ions are connected by six μ2-phenolate oxygen atoms of six salicylic aldehyde ligands, resulting in perfect linear [Ln(III)-Mn(II)-Ln(III)] structures. Magnetic studies of these complexes have been performed and AC susceptibility measurements show the presence of a temperature-dependent out-of-phase ac signal for complexes and indicating single-molecule magnet (SMM) behavior.

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Three pairs of homochiral mononuclear lanthanide complexes, with the general formula [LnH4LRRRRRR/SSSSSS(SCN)2](SCN)2·xCH3OH·yH2O(Ln = Dy (R/S-Dy1), Ho (R/S-Ho1) and Er (R/S-Er1)), have been obtained via self-assembly between chiral macrocyclic ligands and the respective thiocyanates, all of which show a saddle-type conformation with seven-coordinated metal ions. Magnetic measurements revealed that the Dy complex shows field-induced single-ion magnet behaviour, which is rarely reported in a seven-coordinated lanthanide-based SIM encapsulated in a macrocyclic ligand. The absolute configuration of all enantiomers was determined by single crystal X-ray crystallography and confirmed by electronic CD and VCD spectra.

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