Sex-determining region Y box-containing genes are transcription factors with roles in multiple biological processes, including cell differentiation, proliferation, and apoptosis.Sex-determining region Y box-containing...Sex-determining region Y box-containing genes are transcription factors with roles in multiple biological processes, including cell differentiation, proliferation, and apoptosis.Sex-determining region Y box-containing genes have also been shown to act as regulators and biomarkers in the progression of many different cancers, including gynecological cancers such as ovarian, cervical,and endometrial cancer.In this review, we summarize the contrasting regulatory roles of Sex-determining region Y box-containing genes in different gynecological cancers, as promotors with high expression levels or as suppressors with low expression levels.Expression levels of Sex-determining region Y box-containing genes were also identified as biomarkers of clinical features, including International Federation of Gynecology and Obstetrics stage, histopathologic grade together with disease-free survival, and treatment efficacy in patients with gynecological cancers.An understanding of the mechanisms whereby Sex-determining region Y box-containing genes regulate the progression of gynecological cancers will aid in the development of novel diagnostic and therapeutic strategies, while analysis of Sex-determining region Y box-containing expression levels will help to predict the prognosis of patients with gynecological cancers.展开更多
BACKGROUND Sex determining region Y-box 2(SOX2) can promote squamous cell carcinoma(SSC) because it regulates the migration and invasion of several different types of squamous carcinoma cells.However,few studies have ...BACKGROUND Sex determining region Y-box 2(SOX2) can promote squamous cell carcinoma(SSC) because it regulates the migration and invasion of several different types of squamous carcinoma cells.However,few studies have examined the prognostic value of SOX2 and its effect on the epithelial-mesenchymal transition(EMT) in esophageal SSC(ESCC),a cancer characterized by high invasion and rapid metastasis.AIM To verify the relationship of SOX2 and the EMT in ESCC and determine the prognostic value and significance of SOX2 and protein markers of the EMT in ESCC.METHODS One hundred and eighty-five postsurgical ESCC patients were retrospectively examined.Immunohistochemistry was used to detect SOX2,E-cadherin,and vimentin in ESCC tissues.The chi-square test was used to determine the relationships of the expression of these proteins with clinical data.Kaplan-Meier survival curves were used to evaluate factors associated with overall survival(OS).RESULTS SOX2 and vimentin had high expression in ESCC tissues and correlated with the depth of local carcinoma invasion.SOX2 expression had positive correlations with tumor size,vimentin expression,and the EMT,and a negative correlation with Ecadherin expression.Expression of SOX2 and vimentin had negative correlations with OS.SOX2 expression was an independent prognostic risk factor for poor OS in patients with ESCC.CONCLUSION SOX2 expression was an independent risk factor for OS in patients with ESCC and its expression had a positive correlation with the expression of vimentin,a classic marker of the EMT.SOX2 promoted the migration and invasion of ESCC,and this may related to its effect on vimentin in promoting the EMT.展开更多
In order to investigate the relationship between sex dysplasia and sex-determining region Y (SRY) gene, 8 patients with sexual abnormality were analyzed by cytogenetic and molecular genetic methods. Fluorescence in s...In order to investigate the relationship between sex dysplasia and sex-determining region Y (SRY) gene, 8 patients with sexual abnormality were analyzed by cytogenetic and molecular genetic methods. Fluorescence in situ hybridization (FISH) using PY3.4, X alpha satellite, and SRY probes was performed in each case to analyze the sex chromosome translocation and gene translocation. SRY gene was amplified by polymerase chain reaction (PCR) and its mutation was detected by direct sequencing. The results showed that among 8 patients, 5 were positive for SRY and the remaining negative for SRY. In the patients positive for SRY genes, 3 presented testes and the left 2 streak ovaries. In the patients negative for SRY, only one case presented testes, while 2 ovaries. Direct sequencing demonstrated that all SRY genes were normal in the patients positive for SRY genes. FISH technique demonstrated that SRY genes translocated from Ypter to Xpter in 2 46,XX phenotypic males positive for SRY genes. It was concluded that SRY gene is strongly involved in male sex determination, while a sequence of other genes may be taken into account in sexual development.展开更多
目的追踪骨髓间充质干细胞(bone mesenchymal stem cells,BMSCs)在溃疡性结肠炎大鼠模型体内的归巢情况,为BMSCs移植治疗溃疡性结肠炎提供实验基础。方法体外培养扩增Sprague-Dawley(SD)雄性大鼠BMSCs,流式细胞术鉴定BMSCs,采用慢病毒...目的追踪骨髓间充质干细胞(bone mesenchymal stem cells,BMSCs)在溃疡性结肠炎大鼠模型体内的归巢情况,为BMSCs移植治疗溃疡性结肠炎提供实验基础。方法体外培养扩增Sprague-Dawley(SD)雄性大鼠BMSCs,流式细胞术鉴定BMSCs,采用慢病毒载体介导的绿色荧光蛋白(green fluorescent protein,GFP)技术(lentivirus-GFP)对BMSCs进行荧光蛋白标记(Ad-GFP-BMSCs)。SD雌性大鼠被随机分为3组:空白组、模型组、Ad-GFP-BMSCs组。2,4,6-三硝基苯磺酸(2,4,6-trinitrobenzene sulfonic acid,TNBS)诱导溃疡性结肠炎,疾病活动指数(disease activity index,DAI)对各组大鼠进行评估,采用性别交叉移植的方法,尾静脉注射Ad-GFP-BMSCs于雌性大鼠体内,1周后收集结肠标本,对结肠标本进行病理学评估,免疫荧光检测结肠组织GFP表达,PCR检测Y染色体的性别决定区(sex-determining region on the Y chromosome,SRY)基因。结果 TNBS能成功诱导溃疡性结肠炎,与模型组相比,Ad-GFP-BMSCs组DAI评分显著下降(P<0.05)。Lentivirus-GFP成功标记SD大鼠的BMSCs,转染后BMSCs能够稳定表达GFP蛋白,尾静脉注射1周,Ad-GFP-BMSCs组免疫荧光可检测到GFP表达,PCR可检测出SRY基因,空白组和模型组无GFP和SRY基因表达。结论慢病毒载体介导的GFP转染技术和SRY基因可以追踪移植的BMSCs,而且BMSCs通过尾静脉注射可以归巢于受损的结肠组织,这可能为BMSCs移植治疗溃疡性结肠炎提供实验基础。展开更多
基金supported by grants from the National Natural Science Foundation of China (Grant No.81572568 and 81272863)
文摘Sex-determining region Y box-containing genes are transcription factors with roles in multiple biological processes, including cell differentiation, proliferation, and apoptosis.Sex-determining region Y box-containing genes have also been shown to act as regulators and biomarkers in the progression of many different cancers, including gynecological cancers such as ovarian, cervical,and endometrial cancer.In this review, we summarize the contrasting regulatory roles of Sex-determining region Y box-containing genes in different gynecological cancers, as promotors with high expression levels or as suppressors with low expression levels.Expression levels of Sex-determining region Y box-containing genes were also identified as biomarkers of clinical features, including International Federation of Gynecology and Obstetrics stage, histopathologic grade together with disease-free survival, and treatment efficacy in patients with gynecological cancers.An understanding of the mechanisms whereby Sex-determining region Y box-containing genes regulate the progression of gynecological cancers will aid in the development of novel diagnostic and therapeutic strategies, while analysis of Sex-determining region Y box-containing expression levels will help to predict the prognosis of patients with gynecological cancers.
基金Supported by National Natural Science Foundation of China,No. 81860422。
文摘BACKGROUND Sex determining region Y-box 2(SOX2) can promote squamous cell carcinoma(SSC) because it regulates the migration and invasion of several different types of squamous carcinoma cells.However,few studies have examined the prognostic value of SOX2 and its effect on the epithelial-mesenchymal transition(EMT) in esophageal SSC(ESCC),a cancer characterized by high invasion and rapid metastasis.AIM To verify the relationship of SOX2 and the EMT in ESCC and determine the prognostic value and significance of SOX2 and protein markers of the EMT in ESCC.METHODS One hundred and eighty-five postsurgical ESCC patients were retrospectively examined.Immunohistochemistry was used to detect SOX2,E-cadherin,and vimentin in ESCC tissues.The chi-square test was used to determine the relationships of the expression of these proteins with clinical data.Kaplan-Meier survival curves were used to evaluate factors associated with overall survival(OS).RESULTS SOX2 and vimentin had high expression in ESCC tissues and correlated with the depth of local carcinoma invasion.SOX2 expression had positive correlations with tumor size,vimentin expression,and the EMT,and a negative correlation with Ecadherin expression.Expression of SOX2 and vimentin had negative correlations with OS.SOX2 expression was an independent prognostic risk factor for poor OS in patients with ESCC.CONCLUSION SOX2 expression was an independent risk factor for OS in patients with ESCC and its expression had a positive correlation with the expression of vimentin,a classic marker of the EMT.SOX2 promoted the migration and invasion of ESCC,and this may related to its effect on vimentin in promoting the EMT.
文摘In order to investigate the relationship between sex dysplasia and sex-determining region Y (SRY) gene, 8 patients with sexual abnormality were analyzed by cytogenetic and molecular genetic methods. Fluorescence in situ hybridization (FISH) using PY3.4, X alpha satellite, and SRY probes was performed in each case to analyze the sex chromosome translocation and gene translocation. SRY gene was amplified by polymerase chain reaction (PCR) and its mutation was detected by direct sequencing. The results showed that among 8 patients, 5 were positive for SRY and the remaining negative for SRY. In the patients positive for SRY genes, 3 presented testes and the left 2 streak ovaries. In the patients negative for SRY, only one case presented testes, while 2 ovaries. Direct sequencing demonstrated that all SRY genes were normal in the patients positive for SRY genes. FISH technique demonstrated that SRY genes translocated from Ypter to Xpter in 2 46,XX phenotypic males positive for SRY genes. It was concluded that SRY gene is strongly involved in male sex determination, while a sequence of other genes may be taken into account in sexual development.
文摘目的追踪骨髓间充质干细胞(bone mesenchymal stem cells,BMSCs)在溃疡性结肠炎大鼠模型体内的归巢情况,为BMSCs移植治疗溃疡性结肠炎提供实验基础。方法体外培养扩增Sprague-Dawley(SD)雄性大鼠BMSCs,流式细胞术鉴定BMSCs,采用慢病毒载体介导的绿色荧光蛋白(green fluorescent protein,GFP)技术(lentivirus-GFP)对BMSCs进行荧光蛋白标记(Ad-GFP-BMSCs)。SD雌性大鼠被随机分为3组:空白组、模型组、Ad-GFP-BMSCs组。2,4,6-三硝基苯磺酸(2,4,6-trinitrobenzene sulfonic acid,TNBS)诱导溃疡性结肠炎,疾病活动指数(disease activity index,DAI)对各组大鼠进行评估,采用性别交叉移植的方法,尾静脉注射Ad-GFP-BMSCs于雌性大鼠体内,1周后收集结肠标本,对结肠标本进行病理学评估,免疫荧光检测结肠组织GFP表达,PCR检测Y染色体的性别决定区(sex-determining region on the Y chromosome,SRY)基因。结果 TNBS能成功诱导溃疡性结肠炎,与模型组相比,Ad-GFP-BMSCs组DAI评分显著下降(P<0.05)。Lentivirus-GFP成功标记SD大鼠的BMSCs,转染后BMSCs能够稳定表达GFP蛋白,尾静脉注射1周,Ad-GFP-BMSCs组免疫荧光可检测到GFP表达,PCR可检测出SRY基因,空白组和模型组无GFP和SRY基因表达。结论慢病毒载体介导的GFP转染技术和SRY基因可以追踪移植的BMSCs,而且BMSCs通过尾静脉注射可以归巢于受损的结肠组织,这可能为BMSCs移植治疗溃疡性结肠炎提供实验基础。