反义寡脱氧核苷酸及卵泡刺激素对卵巢黏液性囊腺癌细胞增殖细胞核抗原表达的影响  被引量:1

Effects of Antisense Oligodeoxynucleotide and FSH on Expression of PCNA in Primary Culture Cells Derived from Human Ovarian Mucinous Cystadenocarcinom

在线阅读下载全文

作  者:李双[1] 王林[1] 刘合芳[1] 朱长虹[1] 

机构地区:[1]华中科技大学同济医学院计划生育研究所,武汉430030

出  处:《华中科技大学学报(医学版)》2006年第1期68-70,共3页Acta Medicinae Universitatis Scientiae et Technologiae Huazhong

基  金:湖北省卫生厅科研基金资助项目(No.JXIB002)

摘  要:目的观察卵泡刺激素受体(FSHR)反义寡脱氧核苷酸(antisense ODN)及卵泡刺激素(FSH)对体外培养人卵巢黏液性囊腺癌(OMC)细胞增殖细胞核抗原(PCNA)表达的影响。方法OMC细胞与不同浓度的FSH、antisenseODN和无义ODN(nonsense ODN)共培育48、72 h后,采用免疫细胞化学SP法检测细胞核内PCNA的表达。结果FSH明显增强PCNA的表达,而antisense ODN则显著降低PCNA的表达,与对照组比较,差异均有显著性意义(均P<0.05或P<0.01);应用nonsense ODN未观察到其对PCNA表达的影响。同时,antisense ODN可明显拮抗FSH促PCNA表达增加的作用,差异有极显著性意义(P<0.01)。结论在OMC发展过程中,FSH具有一定的促进作用,anti-sense ODN可有效抑制癌细胞的增殖以及FSH的促增殖作用。Objective To observe the effects of antisensc oligodcoxynucleotidc (antisense ODN) to follicle-stimulating hormone receptor (FSHR) and follicle-stimulating hormone (FSH) on the cxprcssion of proliferating cell nuclcar antigen (PCNA) in primary culture cells derived from human ovarian mucinous cystadcnocareinoma (OMC). Methods The primary OMC cells were co-cuhured with antisense ODN and nonsense ODN and FSH with different concentrations for 48 h and 72 h, The expression of PCNA was detected by using SP immunohistochcmistry. Results Compared with that of the control group, the expression of PCNA was increased obviously in FSH groups (P〈0. 05 or P〈0.01). decreased distinctly in antiscnse ODN groups (P 〈0.05 or P〈0. 01) and stable in.nonscnse ODN groups, rcspectively. Mcanwhile, antisensc ODN could obviously antagonize the increased expression of PCNA promoted by FSH (P〈0.01). Conclusion In the development of OMC, FSH might improve it, However, antisense ODN could inhibit OMC cell proliferation and the promoting proliferation caused by FSH,

关 键 词:卵泡刺激素 卵泡刺激素受体 反义寡脱氧核苷酸 卵巢肿瘤 增殖细胞核抗原 

分 类 号:R737.31[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象