In this study 82 bioely tissues of cervical cancer were examined for the Presence of HPV16 E6 gene by PCR.the Positive rate was 73.2%(60/82).The HPV 16 E6 DNA amplified by PCR waslabeled and used as probe to detect HP...In this study 82 bioely tissues of cervical cancer were examined for the Presence of HPV16 E6 gene by PCR.the Positive rate was 73.2%(60/82).The HPV 16 E6 DNA amplified by PCR waslabeled and used as probe to detect HPV E6 gene in the sam.specimens by dot-blot bybridization,thepositive rate was 54.9(45/82).Our rescults showed that the peltive rate of detectiod of HPV 16 E6gene was high in cervical cancer tissue of the Chinese women and cofirmed the close association ofHPV 16 E6 gene with development of cervical cancer.展开更多
OBJECTIVE To determine the association between viral loadof human papillomavirus 16 (HPV16) DNA in the primary focusof cervical carcinoma and HPV16 DNA in pelvic lymph nodes.METHODS The HPV16 DNA load was measured by ...OBJECTIVE To determine the association between viral loadof human papillomavirus 16 (HPV16) DNA in the primary focusof cervical carcinoma and HPV16 DNA in pelvic lymph nodes.METHODS The HPV16 DNA load was measured by fluorescentquantitation polymerase chain reaction (FQ-PCR) in 17 primaryfoci. HPV16 DNA was detected by polymerase chain reaction(PCR) using HPV16 type-specific primers in 296 pelvic lymphnodes which were from 17 cases of cervical cancer.RESULTS The viral load of HPV16 DNA showed statisticallysignificant differences between tumors with a diameter of < 4cm and ≥ 4 cm (P < 0.05). Seven of 17 cervical cancer cases hadHPV16 DNA positive lymph nodes, designated as the positivegroup, while the remaining 10 without positive lymph nodes wasdesignated the negative group. The average load of HPV16 DNAshowed no significant difference between the 2 groups (P > 0.05).The load of HPV16 in the primary lesion was not associated withthat in the lymph nodes. There were 38 HPV16 DNA positivenodes in the total 296 nodes. The rate of positivity of HPV16 DNAin lymph nodes showed statistically significant differences inconsideration of maximum tumor diameter, tumor differentiation,histologic type, depth of myometial infiltration and the metastaticstatus of the nodes, respectively (P < 0.05).CONCLUSION Viral load of HPV16 in the primary cancer focuscorrelated with the quantity of tumor cells in the primary focusbut not with the existence of HPV DNA positive lymph nodes.Detection of HPV DNA may help to find the early metastases thatcannot be evaluated histopathologically, but the prognostic valueof HPV positive lymph nodes needs further examination.展开更多
Objective:To investigate the expression of HPV16 mRNA in normal human keratinocytes transfected with pSV2-neo/16.First human keratinocytes were cultured in the serum-free medium M154.Second,the plasmid pSV2-neo/16 was...Objective:To investigate the expression of HPV16 mRNA in normal human keratinocytes transfected with pSV2-neo/16.First human keratinocytes were cultured in the serum-free medium M154.Second,the plasmid pSV2-neo/16 was transfected into the human keratinocytes using a transfecting reagent.Third,RT-PCR and Southern Blotting were used to detect the expression of HPV16 mRNA and DNA in the transfected keratinocytes,respectively.Results:The expression of HPV 16 mRNA was successfully amplified and an 110bp was ditected by RT-PCR.A 7.9kb fragment was confirmed in the transfected keratinocytes by Southern Blot analysis.Conclusion:HPV 16 mRNA and DNA were successfully detected in the human keratinocytes.展开更多
葡甘露聚糖抑菌护理凝胶(Glucomannan antibacteria care gel,GACG)是本课题组开发的一款已上市的治疗女性阴道炎症的抑菌护理剂。本文介绍了GACG的制备工艺,通过建立高危型HPV 16假病毒感染人胚肾293FT细胞模型,重点研究GACG的主要活...葡甘露聚糖抑菌护理凝胶(Glucomannan antibacteria care gel,GACG)是本课题组开发的一款已上市的治疗女性阴道炎症的抑菌护理剂。本文介绍了GACG的制备工艺,通过建立高危型HPV 16假病毒感染人胚肾293FT细胞模型,重点研究GACG的主要活性成分白芨葡甘露聚糖、积雪草总苷和蛇床子精油对高危型人乳头瘤病毒16(Human papillomavirus type 16,HPV 16)的抗病毒作用。研究发现积雪草总苷和蛇床子精油对高危型HPV 16假病毒具有明显的抗病毒活性,分子对接进一步探究了积雪草苷、羟基积雪草苷以及蛇床子素对HPV 16抑制的可能机制。展开更多
文摘In this study 82 bioely tissues of cervical cancer were examined for the Presence of HPV16 E6 gene by PCR.the Positive rate was 73.2%(60/82).The HPV 16 E6 DNA amplified by PCR waslabeled and used as probe to detect HPV E6 gene in the sam.specimens by dot-blot bybridization,thepositive rate was 54.9(45/82).Our rescults showed that the peltive rate of detectiod of HPV 16 E6gene was high in cervical cancer tissue of the Chinese women and cofirmed the close association ofHPV 16 E6 gene with development of cervical cancer.
文摘OBJECTIVE To determine the association between viral loadof human papillomavirus 16 (HPV16) DNA in the primary focusof cervical carcinoma and HPV16 DNA in pelvic lymph nodes.METHODS The HPV16 DNA load was measured by fluorescentquantitation polymerase chain reaction (FQ-PCR) in 17 primaryfoci. HPV16 DNA was detected by polymerase chain reaction(PCR) using HPV16 type-specific primers in 296 pelvic lymphnodes which were from 17 cases of cervical cancer.RESULTS The viral load of HPV16 DNA showed statisticallysignificant differences between tumors with a diameter of < 4cm and ≥ 4 cm (P < 0.05). Seven of 17 cervical cancer cases hadHPV16 DNA positive lymph nodes, designated as the positivegroup, while the remaining 10 without positive lymph nodes wasdesignated the negative group. The average load of HPV16 DNAshowed no significant difference between the 2 groups (P > 0.05).The load of HPV16 in the primary lesion was not associated withthat in the lymph nodes. There were 38 HPV16 DNA positivenodes in the total 296 nodes. The rate of positivity of HPV16 DNAin lymph nodes showed statistically significant differences inconsideration of maximum tumor diameter, tumor differentiation,histologic type, depth of myometial infiltration and the metastaticstatus of the nodes, respectively (P < 0.05).CONCLUSION Viral load of HPV16 in the primary cancer focuscorrelated with the quantity of tumor cells in the primary focusbut not with the existence of HPV DNA positive lymph nodes.Detection of HPV DNA may help to find the early metastases thatcannot be evaluated histopathologically, but the prognostic valueof HPV positive lymph nodes needs further examination.
文摘Objective:To investigate the expression of HPV16 mRNA in normal human keratinocytes transfected with pSV2-neo/16.First human keratinocytes were cultured in the serum-free medium M154.Second,the plasmid pSV2-neo/16 was transfected into the human keratinocytes using a transfecting reagent.Third,RT-PCR and Southern Blotting were used to detect the expression of HPV16 mRNA and DNA in the transfected keratinocytes,respectively.Results:The expression of HPV 16 mRNA was successfully amplified and an 110bp was ditected by RT-PCR.A 7.9kb fragment was confirmed in the transfected keratinocytes by Southern Blot analysis.Conclusion:HPV 16 mRNA and DNA were successfully detected in the human keratinocytes.