1.Diagnosis and treatment of carotid body tumor——Report of three cases and review of literatures
Bingliang WANG ; Guanyou HUANG ; Weiyu WANG ; Weidong CHEN ; Dongsong YE
Chinese Archives of Otolaryngology-Head and Neck Surgery 2001;8(1):21-23
Three patients with carotid body tumor were treated by surgery in our department from 1994 to 1998. There were 3 females with age from 23 to 40 years old. Among 3 cases, 2 cases were misdiagnosis as neurilemmoma before operation. The size of tumor was 2.5×2.5cm in 1, 3.0×3.0cm in 2. The treatment methods were surgery alone in 2, combined radiotherapy in 1. All patients were cured who had not serious complications. We think that the three symptoms of carotid body tumor are important bases for diagnosis on this disease. However, color B ultrasonography, DSA, CT or MRI also provided informations for useful diagnosis.
2.Clinical effect of adding hMG to the follicular phase long protocol for standard group with normal ovarian reserve function
Yaoyun LIANG ; Shuyun ZHAO ; Guanyou HUANG ; Zhuo CHEN ; Zhu HU
Chinese Journal of Obstetrics and Gynecology 2021;56(5):335-340
Objective:To investigate the impact of adding human menopausal gonadotropin (hMG) for in vitro fertilization-embryo transfer pregnancy outcomes in a standard population of non-advanced age with normal ovarian reserve function using a long follicular phase protocol.Methods:Clinical data of 489 patients with normal ovarian reserve function, who were admitted from January 2018 to January 2020 in the Affiliated Hospital of Guizhou Medical University and underwent in vitro fertilization for the first time with the long follicular phase protocol in fresh cycles, were retrospectively analyzed. The patients were divided into three groups according to whether or not to add urine-derived hMG and the timing of addition: non-addition group (group A), medium-term hMG group (group B1), whole course hMG group (group B2); the laboratory parameters of each group were observed, and the effect of ovulation induction drugs and pregnancy outcomes were compared.Results:The ages of B1 and B2 groups were significantly higher than that of group A ( P=0.019 and P=0.011). The basal FSH level of group B2 was significantly higher than those of group A and group B1 ( P<0.01 and P=0.006), and the basal FSH/LH ratio of group B2 was significantly higher than that of group B1 ( P=0.009). Antral follicle counts of group A and group B1 were significantly higher than that of group B2 ( P=0.007 and P=0.017). The superior embryo rate of group B2 [(47±27)%] was significantly higher than that of group A ( P=0.017). The embryo implantation rate of group B1 was significantly lower than those of group A and group B2 ( P=0.043 and P<0.01). The clinical pregnancy rate of group B2 [76.7% (155/202)] was significantly higher than those of group A ( P=0.039) and group B1 ( P<0.01). The live-birth rate of group B2 [67.3% (136/202)] was significantly higher than those of group A ( P=0.017) and group B1 ( P=0.001). Conclusions:For non-advanced aged patients with normal ovarian reserve function, the long protocol of follicular phase is suitable for those with relatively low ovarian reserve function. Adding hMG in the whole course of ovulation induction after gonadotropin-releasing hormone agonist reduction could improve the pregnancy outcomes by improving the quality of embryos.
3.Effects of fractionated low-dose ionizing radiation on differentiallyexpressed genes in ferroptosis of human bronchial epithelial cells
Min ZHANG ; Lingyu ZHANG ; Yashi CAI ; Huixian LI ; Yanting CHEN ; Guanyou CHEN ; Xin LAN ; Changyong WEN ; Weixu HUANG ; JIanming ZOU ; Huifeng CHEN
Chinese Journal of Radiological Health 2025;34(3):310-317,323
Objective :
To investigate the effects of fractionated low-dose ionizing radiation (LDIR) on the ferroptosis inhuman bronchial epithelial (HBE) cells as well as the associated differentially expressed genes (DEGs), biological processes,and signaling pathways.
Methods :
HBE cells were exposed to different single doses of X-ray irradiation (0, 25, 50, 75, and100 mGy) for 24, 48, and 72 h, respectively. The change in cell viability was detected by MTT assay. Cells were irradiatedwith 0, 25, 50, and 100 mGy X-rays 5 times, with 48 h between each irradiation and a dose rate of 50 mGy/min. Cells wereharvested 24 h after irradiation for the measurement of the expression of ferroptosis-related genes SLC7A11 and GPX4 at themRNA and protein levels, cellular iron content, and the expression of FTH1 and FTL mRNAs. High-throughput sequencingwas used to screen for the DEGs in each dose group, followed by Gene Ontology-Biological Process (GO-BP) analysis,Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, and Gene Set Enrichment Analysis (GSEA).
Results :
Compared with the control group, single-dose LDIR significantly increased cell proliferation at 75 mGy after 24 h (P <0.05), at 50, 75, and 100 mGy after 48 h (P < 0.05), and at 75 and 100 mGy after 72 h (P < 0.05). Compared with the control group, at the end of the fifth fractionated LDIR, SLC7A11 and GPX4 mRNAs decreased at all doses (P < 0.05), SLC7A11protein decreased at all doses, GPX4 protein decreased at 25 and 100 mGy, iron content increased at all doses, and FTH1 andFTL mRNAs decreased at all doses (P< 0.05). Sequencing analysis identified 248, 30, and 291 DEGs and 10, 2, and 9ferrop-tosis-associated genes at the three doses compared to the control. Gene Ontology-Biological Process analysis showed thatDEGs were mainly enriched in biological processes such as response to lipids, cell death, and response to unfolded proteins.Kyoto Encyclopedia of Genes and Genomes analysis showed that DEGs were mainly enriched in the JAK-STAT signalingpathway, lipids and atherosclerosis, ferroptosis, protein processing in the endoplasmic reticulum, and FoxO signalingpath-way. Gene set enrichment analysis showed that DEGs were mainly enriched in ferroptosis, fatty acid degradation, andgluta-thione metabolism.
Conclusion
Fractionated low-dose radiation induced ferroptosis in HBE cells, and DEGs werepre-dominantly enriched in biological processes and signaling pathways related to inflammation, ferroptosis, and endoplasmicre-ticulum stress.