Publications by authors named "Cheng Hong Yin"

Mesenchymal stem cell (MSC)-mediated coupling of osteogenesis and angiogenesis is a critical phenomenon in bone formation. Herein, we investigated the role and mechanism of SGMS1 in the osteogenic differentiation of MSCs and, in combination with osteogenesis and angiogenesis, to discover new therapeutic targets for skeletal dysplasia and bone defects. SGMS1 addition accelerated MSC osteogenic differentiation, whereas SGMS1 silencing suppressed this process.

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Background: Polycystic ovary syndrome is a metabolic and hormonal disorder that is closely linked to oxidative stress. Within individuals diagnosed with PCOS, changes occur in the ovaries, resulting in an excessive buildup of iron and peroxidation of lipids, both of which may be associated with the occurrence of ferroptosis. Baicalein, a flavonoid found in the roots of Scutellaria baicalensis and widely known as Chinese skullcap, is known for its anti-inflammatory and anti-ferroptotic properties, which protect against various diseases.

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Hippocampal neuronal damage may induce cognitive impairment. Neurotrophic tyrosine kinase receptor 1 (NTRK1) reportedly regulates neuronal damage, although the underlying mechanism remains unclear. The present study aimed to investigate the role of NTRK1 in mouse hippocampal neuronal damage and the specific mechanism.

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Background: Miller syndrome is a rare type of postaxial acrofacial dysostosis caused by biallelic mutations in the DHODH gene, which is characterized mainly by craniofacial malformations of micrognathia, orofacial clefts, cup-shaped ears, and malar hypoplasia, combined with postaxial limb deformities like the absence of fifth digits.

Methods: In this study, a prenatal case with multiple orofacial-limb abnormities was enrolled, and a thorough clinical and imaging examination was performed. Subsequently, genetic detection with karyotyping, chromosomal microarray analysis (CMA) and whole-exome sequencing (WES) was carried out.

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  • Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by fragile bones and can be inherited in dominant or recessive patterns, presenting challenges in prenatal counseling due to its diverse manifestations.
  • In a study of ten suspected fetal OI cases, normal results were found through karyotyping and chromosomal microarray analysis, but whole-exome sequencing revealed OI-related genetic variants in all cases, with six being novel.
  • The research underscores the complexity of prenatal OI, including intrafamilial variability and co-existing mutations, and emphasizes the need for further understanding of its pathogenic mechanisms.
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  • Turnpenny-Fry syndrome (TPFS) is a rare genetic disorder marked by global developmental delay, intellectual disability, facial anomalies, and skeletal issues, linked to the PCGF2 gene, which is part of the polycomb repressive complex 1 (PRC1) involved in gene expression regulation.
  • A clinical study focused on a 2.5-year-old boy with GDD and ID included MRI scans and genetic testing, revealing a specific genetic variant (c.194C > T) likely inherited from a mosaic father.
  • The study found that this variant negatively affects the structure and stability of the PCGF2 protein, suggesting its potential role in causing GDD.
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Background: The responses of intravenous immunoglobulin (IVIg) or corticosteroids as the initial treatment on pregnancy with ITP were unsatisfactory. This study aimed to assess the safety and effectiveness of prednisone plus IVIg prednisone or IVIg in pregnant patients with immune thrombocytopenia (ITP).

Methods: Between 1 January 2010 and 31 December 2020, 970 pregnancies diagnosed with ITP at 19 collaborative centers in China were reviewed in this observational study.

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Regulated cell death profoundly affects on the progress of inflammatory and immune responses in various acute inflammatory diseases, as seen in sepsis and trauma. However, the mechanisms underlying CD4 T cells death have not yet been fully addressed. We demonstrated that interferon genes (STING) promoted excessive Poly (ADP-ribose) polymerase 1 (PARP-1) activity stimulated by endotoxin, which in turn induced apoptosis-inducing factor (AIF)-independent but PARP-1 dependent programmed cell death.

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A polycystic ovarian syndrome (PCOS) is the most common endocrine disorder affecting females. Furthermore, it is a heterogeneous disease with a variety of etiologies and outcomes. Patients frequently complain about infertility, irregular menstruation, acne, seborrheic dermatitis, hirsutism, and obesity.

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  • Congenital insensitivity to pain with anhidrosis (CIPA) is caused by mutations in the NTRK1 gene and requires further research to understand its mechanisms.
  • A study used whole-exome sequencing and molecular dynamic analysis to identify a new heterozygous mutation in NTRK1, linked to changes in protein stability and purine metabolism.
  • Results from liquid chromatography-mass spectrometry and quantitative real-time PCR indicated that this variant affects mRNA levels, enhancing understanding of CIPA's genetic basis and offering potential insights for affected families.
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  • Charcot-Marie-Tooth (CMT) 2A is a genetic nerve disorder linked to mutations in the MFN2 gene, which is crucial for mitochondrial function and calcium signaling, but the exact mechanisms of nerve damage remain unclear.
  • This study analyzed a specific CMT2A patient using clinical evaluations, genetic sequencing, and cell metabolic assessments to explore how the identified mutation (c.638T>C: p.Ile213Thr) affects cellular processes.
  • Findings showed that the mutant MFN2 variant disrupted metabolic pathways involving sphingolipids and glycerophospholipids and impaired its ability to bind GTP, providing insights into how these variations could contribute to nerve degeneration in CMT.*
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Severe coronavirus disease 2019 (COVID-19) can manifest as a viral-induced hyperinflammation with multiorgan dysfunction. It has been documented that severe COVID-19 is associated with higher levels of inflammatory mediators than a mild disease, and tracking these markers may allow early identification or even prediction of disease progression. It is well known that C-reactive protein (CRP) is the acute-phase protein and the active regulator of host innate immunity, which is highly predictive of the need for mechanical ventilation and may guide escalation of treatment of COVID-19-related uncontrolled inflammation.

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Background: The incidence of breast cancer among women of reproductive age is increasing, as well as the desire for children at late childbearing age. Identifying factors that may be associated with fetal malformation and maternal and fetal prognosis has gained importance. We describe a 32-year-old woman with breast cancer who gave birth to a son with congenital bilateral cryptorchidism after treatment, with a literature review performed.

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Globally, postpartum hemorrhage (PPH) is the leading cause of maternal death. Women with immune thrombocytopenia (ITP) are at increased risk of developing PPH. Early identification of PPH helps to prevent adverse outcomes, but is underused because clinicians do not have a tool to predict PPH for women with ITP.

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  • * Recent advances in genetic research have identified four genes linked to ASS: SUN5, PMFBP1, TSGA10, and BRDT, shedding light on the disease's underlying causes.
  • * Understanding the genetic mechanisms of ASS paves the way for better molecular diagnosis and improvements in assisted reproductive technologies.
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The aim is to investigate the in vivo and in vitro killing effect of mesothelin chimeric antigen receptor T cells (MESO-CAR-T) in cervical squamous cell carcinoma. MESO-CAR-T cells were successfully constructed. In vitro verification of the killing effect of MESO-CAR-T cells was evaluated in the presence of SiHa cells by the lactate dehydrogenase release assay and cytokine release assay.

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Aim: To explore the feasibility of using mesothelin (MESO) as a tumor-associated antigen (TAA) in cervical squamous cell carcinoma and its function in the development of cervical cancer.

Methods: We collected eight cervical tissue samples of squamous cell carcinoma as the test group and eight samples of cervicitis as the control group from patients who underwent a hysterectomy because of a diagnosis of myoma. Then we used western blotting to screen for a potential TAA in cervical squamous cell carcinoma samples.

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Objective: The aim of this retrospective observational study was to analyze the clinical and pathological characteristics of small-cell neuroendocrine carcinoma of the gynecologic tract (SCNCGT).

Methods: Twenty patients with SCNCGT were enrolled and their clinic-pathological features were analyzed. All patients were treated at the Beijing Obstetrics and Gynecology Hospital, Capital Medical University, China, and were followed up until December 31, 2017.

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Background: In the current society, infertility related to age has become a social problem. The in vitro fertilization (IVF) success rate in women with poor ovarian response (POR) is very low. Dandelion extract T-1 (DE-T1) is an effective component of the extract from the leaves and stems of Taraxacum officinale, which is one of the medicines used in some patients with POR, but its molecular mechanism remains unclear.

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The purpose of this study is to investigate short-term efficacy as defined by the Response Evaluation Criteria in Solid Tumors (RECIST) and pathological response of neoadjuvant chemotherapy (NACT) comprised of paclitaxel and cisplatin (TP) followed by radical surgery in patients with locally advanced cervical cancer (LACC).This is a prospective study involving 61 women with histologically confirmed LACC referred for NACT following radical surgery at Beijing Obstetrics and Gynecology Hospital between April 2013 and January 2015.The efficacy of NACT was evaluated by the RECIST.

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Background: This study was to evaluate the effects of herbal compound 861 (Cpd861) on ski-related novel protein N (SnoN) and transforming growth factor-β1 (TGF-β1) /Smad signaling in rats with bile duct ligation (BDL)-induced hepatic fibrosis, and to explore the mechanisms of Cpd861 on hepatic fibrosis.

Methods: Thirty Wistar male rats were randomly divided into three groups: sham operation, BDL, and Cpd861. To induce hepatic fibrosis, BDL and Cpd861 group rats underwent bile duct ligation.

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Article Synopsis
  • A diagnostic model was created to predict acute Mycoplasma pneumoniae infections in elderly patients with community-acquired pneumonia, analyzing 456 individuals.
  • Key factors for prediction included age 70+, elevated serum cTNT levels, lobar consolidation, mediastinal lymphadenopathy, and specific antibody titer levels.
  • The model achieved a high diagnostic accuracy with an ROC curve score of 0.923, indicating that a score of 7 or higher suggests an acute M. pneumoniae infection in this patient group.
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The purpose of this prospective cohort study is to evaluate the importance of screening and its diagnostic accuracy compared with the pathological diagnosis of cervical intraepithelial neoplasia (CIN) with vaginal intraepithelial neoplasia (VAIN).The prospective study enrolled 419 patients (pts) and was conducted between February 1, 2015 and January 31, 2016 at Beijing Obstetrics and Gynecology Hospital, Capital Medical University.All enrolled pts underwent multipoint biopsy of cervix and vaginal wall directed by colposcopy.

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Background: Premature ovarian failure (POF) is a disease that affects female fertility but has few effective treatments. Ovarian reserve function plays an important role in female fertility. Recent studies have reported that hydrogen can protect male fertility.

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Increased fibronectin (FN) expression has an important role during liver fibrosis. The present study examined FN expression in rats subjected to carbon tetrachloride (CCl4)‑induced liver fibrosis. In addition, the potential mechanisms underlying fibrogenesis were investigated by exposing hepatic stellate cells (HSCs) to transforming growth factor‑β (TGF‑β), which is a known inducer of myofibroblastic transformation of HSCs.

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