694 results match your criteria: "Department of Obstetrics and Gynecology,the First Affiliated Hospital of Zhengzhou University[Affiliation]"

Background: Patients with choriocarcinoma (CC) accompanying chemoresistance conventionally present a poor prognosis. Whether ras protein activator like-1 (RASAL1) functions as a tumor promoter or suppressor depends on tumor types. However, the role of RASAL1 in process of chemoresistance of CC and underlying molecular mechanism remain elusive.

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Endometrial cancer (EC) is a highly heterogeneous malignancy characterized by varied pathology and prognoses, and the heterogeneity of its cancer cells and the tumor microenvironment (TME) remains poorly understood. We conducted single-cell RNA sequencing (scRNA-seq) on 18 EC samples, encompassing various pathological types to delineate their specific unique transcriptional landscapes. Cancer cells from diverse pathological sources displayed distinct hallmarks labeled as immune-modulating, proliferation-modulating, and metabolism-modulating cancer cells in uterine clear cell carcinomas (UCCC), well-differentiated endometrioid endometrial carcinomas (EEC-I), and uterine serous carcinomas (USC), respectively.

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Objectives: The roles of magnetic resonance imaging (MRI) -based radiomics approach and deep learning approach in cervical adenocarcinoma (AC) have not been explored. Herein, we aim to develop prognosis-predictive models based on MRI-radiomics and clinical features for AC patients.

Methods: Clinical and pathological information from one hundred and ninety-seven patients with cervical AC was collected and analyzed.

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Article Synopsis
  • The medical school learning environment (MSLE) significantly affects students' health and academic success, with perceptions varying by grade level.
  • A study of 10,901 medical students used the Johns Hopkins Learning Environment Scale (JHLES) to categorize perceptions and reveal that third and fourth graders had notably lower scores compared to freshmen.
  • The research confirmed that students in grades 3 and 4 were more negatively impacted by MSLE, leading to the creation of a nomogram that helps predict the likelihood of low JHLES scores among students.
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Trends in the antimicrobial susceptibility among Chinese neonates from 2012 to 2021: a multicenter study.

Antimicrob Resist Infect Control

July 2024

Department of Pediatrics, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, 1665 Kongjiang Road, Yangpu District, Shanghai, 200092, China.

Article Synopsis
  • Antibiotic resistance is a significant global health problem, particularly in China, where there is limited data on antimicrobial susceptibility trends in neonates.
  • A study conducted from 2012 to 2021 across 17 hospitals in China found that resistance patterns of common pathogens in full-term neonates with invasive bacterial infections varied, with some pathogens showing improved susceptibility to certain antibiotics while others worsened.
  • Notably, Escherichia coli's susceptibility decreased for certain antibiotics, while group B Streptococcus and Staphylococcus aureus showed increased susceptibility, highlighting both improvements and concerns in neonatal healthcare.
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[The application value of whole exome sequencing technology in diagnosis of hereditary renal cysts].

Zhonghua Yi Xue Za Zhi

July 2024

Center of Genetic and Prenatal Diagnosis, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

The data of 57 renal cyst patients who visited the First Affiliated Hospital of Zhengzhou University from January 2023 to March 2024 were retrospectively analyzed. The age of patients ranged from three months to 60 years old, with 31 males and 26 females. The whole exome sequencing (WES) detected pathogenic or suspected pathogenic (P/LP) variants in 48 renal cystic probands, with a detection rate of 84.

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NOP2, a member of the NOL1/NOP2/SUN domain (NSUN) family, is responsible for catalyzing the posttranscriptional modification of RNA through 5-methylcytosine (m5C). Dysregulation of m5C modification has been linked to the pathogenesis of various malignant tumors. Herein, we investigated the expression of NOP2 in lung adenocarcinoma (LUAD) tissues and cells, and found that it was significantly upregulated.

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A novel HOIP frameshift variant alleviates NF-kappaB signalling and sensitizes cells to TNF-induced death.

Biochim Biophys Acta Mol Basis Dis

October 2024

Key Laboratory of Molecular Biophysics of the Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China. Electronic address:

Background: HOIP is the catalytic subunit of the E3 ligase complex (linear ubiquitin chain assembly complex), which is able to generate linear ubiquitin chains. However, the role of rare HOIP functionally deficient variants remains unclear. The pathogenic mechanism and the relationship with immune deficiency phenotypes remain to be clarified.

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Introduction: Previous observational studies have shown that polycystic ovary syndrome (PCOS) was associated with adverse pregnancy and perinatal outcomes. However, it remains controversial whether PCOS is an essential risk factor for these adverse pregnancy and perinatal outcomes. We aimed to use instrumental variables in a two-sample Mendelian randomization (MR) study to determine causality between PCOS and adverse pregnancy and perinatal outcomes.

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Introduction: Diabetic nephropathy (DN) is the leading cause of end-stage renal disease. Due to its complex pathogenesis, new therapeutic agents are urgently needed. (Blume) Miq.

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Fertility preservation in male adolescents with cancer (2011-2020): A retrospective study in China.

Cancer Med

June 2024

NHC Key Laboratory of Male Reproduction and Genetics, Guangdong Provincial Reproductive, Science Institute, Guangdong Provincial Fertility Hospital, Guangzhou, Guangdong, China.

Background: According to the studies, more than 80% of pediatric patients with cancer can achieve a survival rate greater than 5 years; however, long-term chemotherapy and/or radiation therapy may seriously affect their reproductive ability. Fertility preservation in adolescents with cancer in China was initiated late, and related research is lacking. Analyze data to understand the current situation and implement measures to improve current practices.

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The spike-in plasmid method was utilized to perform an analysis on meconium and second-pass feces, yielding both relative and absolute quantitative results. With the absolute quantitative data, the abundance of bacteria in 17 meconium samples and 17 second-pass fecal samples were found to be 1.14 × 10 and 1.

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Prenatal exome sequencing for morphologically normal fetus: Should we be doing it?

Prenat Diagn

June 2024

Department of Obstetrics and Gynecology, Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Article Synopsis
  • The study explored the effectiveness of prenatal exome sequencing (pES) in detecting genetic issues in fetuses that appeared normal based on physical exams.
  • Out of 254 families analyzed, 8 (3.1%) were found to have abnormal findings, with most cases related to specific genetic disorders.
  • The results highlight the importance of genetic counseling throughout the pES process, ensuring families receive clear information about potential findings and implications for future pregnancies.
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Molecular findings in patients for whole exome sequencing and mitochondrial genome assessment.

Clin Chim Acta

July 2024

Genetics and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. Electronic address:

Objective: Whole exome sequencing (WES) is becoming more widely used as a diagnostic tool in the field of medicine. In this article, we reported the diagnostic yield of WES and mitochondrial genome assessment in 2226 consecutive cases in a single clinical laboratory.

Materials And Methods: We retrospectively analyzed consecutive WES reports from 2226 patients with various genetic disorders.

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Thymus cell antigen 1 () has been proven to play pivotal roles in many diseases. However, we do not fully understand its functional mechanism, especially in lung squamous cell carcinoma (LUSC). Here, we aimed to perform a comprehensive analysis to explore the expression and prognostic values of in LUSC using bioinformatic technology.

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[Clinical analysis of 80 patients with oblique vaginal septum syndrome].

Zhonghua Fu Chan Ke Za Zhi

May 2024

Department of Obstetrics and Gynecology, The Second Hospital of Hebei Medical University, Shijiazhuang 050000, China.

To investigate the clinical features, diagnosis and treatment of oblique vaginal septum syndrome (OVSS). The clinical data of 80 patients with OVSS admitted to The Second Hospital of Hebei Medical University from July 2005 to July 2023 were retrospectively analyzed. According to the classification system of OVSS proposed by Female Genital Anomalies Study Group, Chinese Obstetricians and Gynecologists Association in 2021, the patients were divided into four groups.

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Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome.

Orphanet J Rare Dis

May 2024

Genetic and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.

Article Synopsis
  • Marfan syndrome (MFS) is a hereditary connective tissue disorder primarily linked to mutations in the FBN1 gene, which can lead to various clinical symptoms in affected individuals.
  • A study involving a four-generation Chinese family used exome sequencing and various analyses to identify and assess the pathogenicity of genetic variants in FBN1, revealing a significant intronic variant causing MFS symptoms.
  • The research highlights the necessity of evaluating intronic variants' effects on mRNA and protein structure, leading to an understanding of how such modifications can disrupt normal gene function and contribute to MFS.
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Ga-labeled TMTP1 radiotracer for PET imaging of cervical cancer.

Am J Nucl Med Mol Imaging

April 2024

Department of Nuclear Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030, Hubei, China.

Molecular imaging enables visualization and characterization of biological processes that influence tumor behavior and response to therapy. The TMTP1 (NVVRQ) peptide has shown remarkable affinity to highly metastatic tumors and and its potential receptor is aminopeptidase P2. In this study, we have designed and synthesized a Ga-labeled cyclic TMTP1 radiotracer (Ga-DOTA-TMTP1), for PET imaging of cervical cancer.

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EGF-like growth factors upregulate pentraxin 3 expression in human granulosa-lutein cells.

J Ovarian Res

May 2024

Department of Obstetrics and Gynecology, BC Children's Hospital Research Institute, University of British Columbia, Room 317, 950 West 28th Avenue, Vancouver, BC, V5Z 4H4, Canada.

Article Synopsis
  • EGF-like factors, specifically amphiregulin (AREG), betacellulin (BTC), and epiregulin (EREG), are essential in regulating the ovulation process and influencing the production of the protein PTX3 in human granulosa-lutein (hGL) cells.
  • * The study found that these EGF-like factors enhance the expression and production of PTX3, crucial for maintaining the extracellular matrix during cumulus expansion, through the activation of the ERK1/2 signaling pathway.
  • * The upregulation of PTX3 by AREG, BTC, and EREG is dependent on the epidermal growth factor receptor (EGFR), as inhibiting or knocking down EGFR reversed the
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Corrigendum: Therapeutic strategies targeting folate receptor α for ovarian cancer.

Front Immunol

April 2024

Department of Laboratory Medicine, Obstetrics & Gynecology and Pediatrics, West China Second University Hospital, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Development and Related Diseases of Women and Children Key Laboratory of Sichuan Province, Center of Growth, Metabolism and Aging, State Key Laboratory of Biotherapy and Collaborative Innovation Center of Biotherapy, Sichuan University, Chengdu, Sichuan, China.

Article Synopsis
  • This text mentions a correction to a previous article identified by the DOI: 10.3389/fimmu.2023.1254532.
  • The correction likely addresses errors or inaccuracies found in the original publication.
  • Such corrections are common in academic research to ensure the integrity and accuracy of scientific information.
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Noninvasive twin genotyping for recessive monogenic disorders by relative haplotype dosage.

Prenat Diagn

August 2024

Department of Fetal Medicine & Prenatal Diagnosis Center, Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai, China.

Objective: To establish a haplotype-based noninvasive prenatal testing (NIPT) workflow for single-gene recessive disorders that adapt to dizygotic (DZ) twin pregnancies.

Method: Twin pregnancies at risk of Duchenne muscular dystrophy, Becker muscular dystrophy, hemophilia B, spinal muscular atrophy, phenylketonuria, and nonsyndromic hearing loss were recruited. For subsequent analysis, capture sequencing targeting highly heterozygotic single nucleotide polymorphism sites was conducted.

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Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients.

Orphanet J Rare Dis

April 2024

The Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Jianshe Rd, Erqi District, 450052, Zhengzhou, Henan, China.

Article Synopsis
  • Primary periodic paralysis (PPP) is a genetic disorder leading to episodes of muscle weakness, categorized based on potassium levels during attacks; diagnosis relies on clinical symptoms and genetic testing.
  • In a study of 37 Chinese patients, 59.5% had identified genetic variants, mainly in the SCN4A and CACNA1S genes, with comparable detection rates between gene panel testing and whole-exome sequencing.
  • The findings highlight SCN4A variants as the primary cause of PPP in this cohort, revealing novel mutations and expanding the understanding of genetic causes of the disorder.
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RNA methylation is widespread in nature. Abnormal expression of proteins associated with RNA methylation is strongly associated with a number of human diseases including cancer. Increasing evidence suggests that targeting RNA methylation holds promise for cancer treatment.

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Background: Several risk factors have been identified that compromise the treatment outcome in patients with early-to-mid-stage cervical cancer (CC) who are primarily treated with radical surgery. However, there is no report on the impact of intraoperative frozen pathology examination of vaginal margins on the prognosis of patients with CC. This study aimed to conduct a randomized controlled trial (RCT) to determine whether selective vaginal resection can reduce the incidence of operative complications and the risk of postoperative radiotherapy.

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