Publications by authors named "Lingling Weng"

Article Synopsis
  • Colloidal gold nanoparticles (AuNPs) are critical for chemical sensing and therapeutic applications, necessitating effective surface functionalization for stability in biological environments.
  • Traditional methods use thiol groups for bonding, but these can be complex and not resilient to certain conditions, leading to the exploration of alkyne derivatives as a preferable alternative.
  • The study shows that alkyne derivatives provide easier preparation, higher stability, and better conjugation efficiency, and highlights their effectiveness in detecting hydrogen peroxide and streptavidin proteins.
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Background: Nocebo and placebo effects, i.e., adverse or beneficial treatment effects, respectively, putatively due to expectancies can modulate pain and itch.

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Objectives: To investigate the indications of obstetric emergency hysterectomy and analyze the clinical effects of subtotal hysterectomy and total hysterectomy.

Methods: We included 247 hospitalized women who had undergone abdominal hysterectomy due to obstetric reasons in Fujian Province Maternity and Child Health Hospital (a provincial class-A hospital) and Ningde People's Hospital (a primary Class-B hospital) between January 2002 and December 2018. We identified surgical indications and clinical characteristics of the patients.

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  • * High levels of COMMD3 are linked to worse overall survival and disease-free survival for HCC patients, as well as advanced cancer stages and vascular invasion.
  • * Silencing COMMD3 in HCC cells reduces their migration, invasion, and tumor growth in mouse models, indicating COMMD3's potential as a target for HCC treatment.
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Nocebo effects, that is, negative treatment outcomes due to negative expectancies, can increase itch. Moreover, indirect evidence has shown that nocebo hyperknesis can generalize to another itch modality. Knowledge on response generalization can help to prevent and decrease negative effects.

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Pain and other somatosensory sensations, such as itch, can be effectively decreased by placebo effects and increased by nocebo effects. There are indications that placebo effects on pain generalize to other sensations and that nocebo effects generalize within itch modalities. However, it has not yet been investigated whether learned effects can generalize within pain stimulus modalities or from pain to itch.

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  • Despite various treatment strategies for hepatocellular carcinoma (HCC), patient survival rates remain low, highlighting a need for effective therapies.
  • Asparagus polysaccharide (ASP) has been shown to significantly inhibit the proliferation, migration, invasion, and angiogenesis of HCC cells, particularly under hypoxic conditions, which are common in tumors.
  • The study indicates that ASP's effects may involve down-regulating proteins associated with hypoxia, such as HIF-1α and VEGF, through inhibition of key signaling pathways, thus offering potential therapeutic benefits for HCC patients.
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Purpose: MicroRNAs (miRNAs) participate in a variety of biological processes, including tumorigenesis, progression, invasion, and drug resistance to multiple cancers. Phosphatase and tensin homolog (PTEN) is a cancer suppressor gene that has been certified to be regulated by miRNAs in various tumors, including colorectal cancer (CRC). In this review, we screened articles focusing on low PTEN expression in CRC, observed the expression of related miRNAs, analyzed their correlation and relationship with clinicopathological features, and discussed the possibility of these miRNAs as prognostic molecules.

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This study included fifty-eight isolates of from the oral cavity of snakes that were recruited from clinical cases, captive and wild snakes. The minimum inhibitory concentrations (MICs) for the determination of susceptibility were identified by the broth microdilution method. Polymerase chain reaction (PCR) was employed to detect -lactamases genes.

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Hepatocellular carcinoma (HCC) has become a leading cause of cancer-associated mortality worldwide and is thus of great concern. Although various chemotherapeutic drugs are currently used for the treatment of HCC, severe side effects associated with these treatments have prompted interest in novel therapies, including the use of certain biological macromolecules such as polysaccharides. Several studies have shown that polysaccharides have anticancer and antiproliferative effects on HCC.

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Peptide dendrimers are a novel type of macromolecules with precise structure, which can be used as drug target vector and controlled-release carrier. So it is valuable to study. In this paper, novel peptide dendrimers PDL-GB2 and PDL-G2 were prepared according to divergent procedure with four-orientation molecule as the core and L-lysine as the branch unit.

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Liver cancer is one of leading digestive malignancies with high morbidity and mortality. There is an urgent need for the development of novel therapies for this deadly disease. It has been proven that asparagus polysaccharide, one of the most active derivates from the traditional medicine asparagus, possesses notable antitumor properties.

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Hepatocellular carcinoma (HCC) is one of the most aggressive malignancies in the world whose chemoprevention became increasingly important in HCC treatment. Although the anticancer effects of asparagus constituents have been investigated in several cancers, its effects on hepatocellular carcinoma have not been fully studied. In this study, we investigated the anticancer effects of the deproteinized asparagus polysaccharide on the hepatocellular carcinoma cells using the in vitro and in vivo experimental model.

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Personalized oncology significantly relies on the development of cancer theranostic agents to integrate cancer therapeutics and diagnostics. Current most common strategy for development of such multifunctional agents requires multistep chemical conjugation with cancer targeted ligands, contrast agents and therapeutic agents. Here we report the chemical synthesis and biological characterization of a new heptamethine dye, termed as IR-808DB, natively with multifunctional characteristics of cancer targeting, near-infrared fluorescence imaging, and efficient anticancer activity.

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New quinolone derivatives bearing a cis- or trans-cyclohexane side chain at the C-7 position have been synthesized and evaluated for their antibacterial activities against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa using the agar dilution method. The activities of compound 53 against these three bacteria were superior to those of the reference drug lomefloxacin. Compounds bearing a cis-cyclohexane side chain generally exhibited greater antibacterial activity than their corresponding trans-isomers.

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Objective: To detect the influence of raloxifene (RLX) on fracture healing in rabbit.

Methods: Eight healthy New Zealand white rabbits (44 females and 36 males) weighing 1.9-2.

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In the title compound, C(16)H(17)FN(2)O(4)·H(2)O, the dihedral angle between the heterocyclic ring and the benzene ring is 5.77 (9)°, that between the heterocycle and the ethoxy-carbonyl plane is 15.5 (1)°, and that between the heterocyclic ring and the cyclopropane ring is 67.

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A novel derivative of oxytocin containing nonprotein amino acid L-alpha, beta-diaminopropionic acid (L-Dap) was synthesized by 7+2 fragment combination in solution. N beta of all the amino acid necessary was protected by carbobenzoxy (Z) and N beta of L-Dap was protected by tert. -butoxycarbonyl (Boc) .

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Article Synopsis
  • The objective of the study was to create new derivatives of 5-fluorouracil that include 2-5 carbon alkanoic acid.
  • Researchers used a "one-pot" method involving hydrolysis and protection of 5-fluorouracil to achieve high yields of the desired compounds (75%-85%).
  • The study resulted in the synthesis of 16 new 5-fluorouracil derivatives, confirmed by spectral analysis, demonstrating effective methods for producing N1 and N3-substituted variants.
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The purpose of this study was to determine the effects of piperazinyl estrone, a new estrogen derivative, on bone turnover, bone mass and uterine weight in female aged rats. Thirty-two Sprague-Dawley female rats at the age of 22 months were treated with vehicle or with piperazinyl estrone (P-E) at 0.5, 1 and 2 mg/kg/day, subcutaneous injection for 1 month.

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Objective: To identify the effect of XW630 on the expression of type I collagen in the epiphyseal plates of mice.

Methods: The immunohistochemical method was used to measure the change of type I collagen protein after being treated with XW630.

Results: With 10(-7) mol/L or 10(-7) mol/L of XW630, the area of positive stain cells in every zone increased significantly compared to the control group.

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Objective: To establish an HPLC method and a non-aqueous titration for the determination of piperazinylethylestrone drug substance, and an HPLC method for the determination of piperazinylethylestrone in dog plasma.

Methods: Anhydrous acetic acid as solvent, 0.1 mol/L perchloric acid as titrant, crystal violet solution as indicator to establish non-aqueous titrations and ODS column as stationary phase, methanol and a mixture of 0.

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Objective: To demonstrate the histomorphometric changes of postmenopausal osteoporosis (PMO) goat model after bilateral ovariectomy (OVX).

Methods: Fifteen female goats were randomly enrolled into four groups: 3 goats without any treatment (group C), 3 goats sham-operated only (group S), 4 goats 6 months after OVX (group OVX6M), 5 goats 18 months after OVX (group OVX18M). On the 21st and 9th day prior to sacrifice, tetracycline was given to them in order to label the bone for dynamic study.

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This study was performed to investigate the mechanism of an anti-osteoporosis new drug XW630 for promoting the osteogenic action. Osteoblast clone was cultivated from SD adult rat calvaria in vitro, the estrogen receptor messenger RNA(ERmRNA) expression in the osteoblasts of rats was detected directly with high-sensitive RT-PCR firstly. The results indicated that XW630 can significantly promote ERmRNA expression in osteoblasts in the time-dependent manner.

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