蚌埠医学院学报
蚌埠醫學院學報
방부의학원학보
ACTA ACADEMIAE MEDICINAE BENGBU
2014年
6期
711-713,717
,共4页
陈素莲%朱丽华%卢晓辉%赵遵兰%王洋洋%周继红%陈昌杰%杨清玲
陳素蓮%硃麗華%盧曉輝%趙遵蘭%王洋洋%週繼紅%陳昌傑%楊清玲
진소련%주려화%로효휘%조준란%왕양양%주계홍%진창걸%양청령
乳腺肿瘤%长链非编码RNA%HOX转录反义RNA%三氧化二砷
乳腺腫瘤%長鏈非編碼RNA%HOX轉錄反義RNA%三氧化二砷
유선종류%장련비편마RNA%HOX전록반의RNA%삼양화이신
breast neoplasms%long-chain non-coding RNA%HOX transcript antisense RNA%arsenic trioxide
目的:探讨长链非编码RNA HOX转录反义RNA( HOTAIR)在乳腺癌组织和细胞中的表达情况及三氧化二砷( As2 O3)对HOTAIR基因表达的影响。方法:实时定量PCR检测在乳腺癌癌旁组织与癌组织中长链非编码RNA HOTAIR mRNA的表达,筛选高表达HOTAIR的乳腺癌细胞株,检测 As2 O3对 HOTAIR mRNA 表达的作用。先观察比较乳腺癌与癌旁组织中HOTAIR的表达,再检测乳腺癌细胞株中HOTAIR的表达,以及As2 O3作用后MCF-7细胞中HOTAIR的表达变化。结果:乳腺癌组织中HOTAIR mRNA表达量为0.011±0.005,癌旁组织未见表达;乳腺癌细胞株SKBR-3和MAD-MB-231细胞均未表达HOTAIR mRNA,MCF-7细胞株高表达HOTAIR mRNA(1±0.236);在As2O3作用下,MCF-7细胞中HOTAIR mRNA表达较空白组明显下降(P<0.01)。结论:HOTAIR与乳腺癌的发展可能相关,As2O3可以抑制其表达。
目的:探討長鏈非編碼RNA HOX轉錄反義RNA( HOTAIR)在乳腺癌組織和細胞中的錶達情況及三氧化二砷( As2 O3)對HOTAIR基因錶達的影響。方法:實時定量PCR檢測在乳腺癌癌徬組織與癌組織中長鏈非編碼RNA HOTAIR mRNA的錶達,篩選高錶達HOTAIR的乳腺癌細胞株,檢測 As2 O3對 HOTAIR mRNA 錶達的作用。先觀察比較乳腺癌與癌徬組織中HOTAIR的錶達,再檢測乳腺癌細胞株中HOTAIR的錶達,以及As2 O3作用後MCF-7細胞中HOTAIR的錶達變化。結果:乳腺癌組織中HOTAIR mRNA錶達量為0.011±0.005,癌徬組織未見錶達;乳腺癌細胞株SKBR-3和MAD-MB-231細胞均未錶達HOTAIR mRNA,MCF-7細胞株高錶達HOTAIR mRNA(1±0.236);在As2O3作用下,MCF-7細胞中HOTAIR mRNA錶達較空白組明顯下降(P<0.01)。結論:HOTAIR與乳腺癌的髮展可能相關,As2O3可以抑製其錶達。
목적:탐토장련비편마RNA HOX전록반의RNA( HOTAIR)재유선암조직화세포중적표체정황급삼양화이신( As2 O3)대HOTAIR기인표체적영향。방법:실시정량PCR검측재유선암암방조직여암조직중장련비편마RNA HOTAIR mRNA적표체,사선고표체HOTAIR적유선암세포주,검측 As2 O3대 HOTAIR mRNA 표체적작용。선관찰비교유선암여암방조직중HOTAIR적표체,재검측유선암세포주중HOTAIR적표체,이급As2 O3작용후MCF-7세포중HOTAIR적표체변화。결과:유선암조직중HOTAIR mRNA표체량위0.011±0.005,암방조직미견표체;유선암세포주SKBR-3화MAD-MB-231세포균미표체HOTAIR mRNA,MCF-7세포주고표체HOTAIR mRNA(1±0.236);재As2O3작용하,MCF-7세포중HOTAIR mRNA표체교공백조명현하강(P<0.01)。결론:HOTAIR여유선암적발전가능상관,As2O3가이억제기표체。
Objective:To investigate the expression of long-chain non-coding HOX transcript antisense RNA(HOTAIR) in breast cancer tissues and cells,and effects of arsenic trioxide( As2 O3 ) on its expression. Methods:The expressions of long-chain non-coding HOTAIR mRNA in breast carcer tissue and pericarcinomatous tissue were detected using real-time fluorescence quantitative PCR. Breast cancer cell lines with high expression HOTAIR was screened,the effect of As2 O3 on the expression of HOTAIR mRNA was detected. The expressions of HOTAIR between breast cancer tissue, pericarcinomatous tissue and breast cancer cell lines were compared. The HOTAIR expression in MCF-7 cells treated with As2 O3 was detected. Results:The expression quantity of HOTAIR mRNA in breast cancer was 0. 011 ± 0. 005,no expression of HOTAIR was found in pericarcinomatous tissue. The HOTAIR mRNA expression was not found in SKBR-3 and MAD-MB-231 cells. The high expression of HOTAIR mRNA(1 ± 0. 236) was detected in MCF-7 cells. The expression level of HOTAIR mRNA in MCF-7 cells treated with As2O3 was significantly lower than that in blank group(P<0. 01). Conclusions:The HOTAIR expression is associated with the incidence of breast cancer,and As2 O3 can inhibit its expression.