山东医药
山東醫藥
산동의약
Shandong Medical Journal
2015年
32期
17-19
,共3页
苏强%马妮娜%李琴%俞静%张晨光
囌彊%馬妮娜%李琴%俞靜%張晨光
소강%마니나%리금%유정%장신광
卵巢肿瘤%卵巢透明细胞癌%丁酸钠%顺铂%细胞活性%增殖蛋白%凋亡蛋白
卵巢腫瘤%卵巢透明細胞癌%丁痠鈉%順鉑%細胞活性%增殖蛋白%凋亡蛋白
란소종류%란소투명세포암%정산납%순박%세포활성%증식단백%조망단백
ovarian neoplasms%ovarian clear cell carcinoma%sodium butyrate%cisplatin%cell viability%proliferin%apoptin
目的:观察丁酸钠联合顺铂对卵巢透明细胞癌ES-2细胞活性及增殖的影响。方法将对数生长期的卵巢透明细胞癌ES-2细胞随机分为观察组和对照组。观察组分别加入1、2、4、6 mmol/L的丁酸钠和5μg/mL顺铂,对照组分别加入与观察组相同浓度的丁酸钠。采用MMT法检测两组细胞活性,Western blotting 法检测两组凋亡蛋白( c-PAPP、c-Caspase-3)和增殖蛋白( ERK、p-ERK)相对表达量。结果观察组加入1、2、4、6 mmol/L丁酸钠和顺铂细胞活性分别为51%±3%、39%±2%、22%±2%、11%±1%,多组间及组内两两比较,P均<0.05;对照组加入1、2、4、6 mmol/L丁酸钠细胞活性分别为88%±4%、76%±3%、69%±2%、54%±2%,多组间及组内两两比较,P均<0.05;两组加入相同浓度丁酸钠细胞活性比较,P均<0.05。随着丁酸钠浓度增加,两组凋亡蛋白c-PAPP、c-Caspase-3相对表达量逐渐升高,增殖蛋白ERK、p-ERK相对表达量逐渐降低。与对照组同浓度丁酸钠比较,观察组1、2、4、6 mmol/L丁酸钠和顺铂c-PAPP、c-Caspase-3蛋白表达均升高,1、6 mmol/L丁酸钠和顺铂ERK、p-ERK蛋白表达均降低;两组比较,P均<0.05。结论丁酸钠联合顺铂可降低卵巢透明细胞癌ES-2细胞活性,抑制其增殖、促进其凋亡;丁酸钠浓度越高,上述作用越明显。
目的:觀察丁痠鈉聯閤順鉑對卵巢透明細胞癌ES-2細胞活性及增殖的影響。方法將對數生長期的卵巢透明細胞癌ES-2細胞隨機分為觀察組和對照組。觀察組分彆加入1、2、4、6 mmol/L的丁痠鈉和5μg/mL順鉑,對照組分彆加入與觀察組相同濃度的丁痠鈉。採用MMT法檢測兩組細胞活性,Western blotting 法檢測兩組凋亡蛋白( c-PAPP、c-Caspase-3)和增殖蛋白( ERK、p-ERK)相對錶達量。結果觀察組加入1、2、4、6 mmol/L丁痠鈉和順鉑細胞活性分彆為51%±3%、39%±2%、22%±2%、11%±1%,多組間及組內兩兩比較,P均<0.05;對照組加入1、2、4、6 mmol/L丁痠鈉細胞活性分彆為88%±4%、76%±3%、69%±2%、54%±2%,多組間及組內兩兩比較,P均<0.05;兩組加入相同濃度丁痠鈉細胞活性比較,P均<0.05。隨著丁痠鈉濃度增加,兩組凋亡蛋白c-PAPP、c-Caspase-3相對錶達量逐漸升高,增殖蛋白ERK、p-ERK相對錶達量逐漸降低。與對照組同濃度丁痠鈉比較,觀察組1、2、4、6 mmol/L丁痠鈉和順鉑c-PAPP、c-Caspase-3蛋白錶達均升高,1、6 mmol/L丁痠鈉和順鉑ERK、p-ERK蛋白錶達均降低;兩組比較,P均<0.05。結論丁痠鈉聯閤順鉑可降低卵巢透明細胞癌ES-2細胞活性,抑製其增殖、促進其凋亡;丁痠鈉濃度越高,上述作用越明顯。
목적:관찰정산납연합순박대란소투명세포암ES-2세포활성급증식적영향。방법장대수생장기적란소투명세포암ES-2세포수궤분위관찰조화대조조。관찰조분별가입1、2、4、6 mmol/L적정산납화5μg/mL순박,대조조분별가입여관찰조상동농도적정산납。채용MMT법검측량조세포활성,Western blotting 법검측량조조망단백( c-PAPP、c-Caspase-3)화증식단백( ERK、p-ERK)상대표체량。결과관찰조가입1、2、4、6 mmol/L정산납화순박세포활성분별위51%±3%、39%±2%、22%±2%、11%±1%,다조간급조내량량비교,P균<0.05;대조조가입1、2、4、6 mmol/L정산납세포활성분별위88%±4%、76%±3%、69%±2%、54%±2%,다조간급조내량량비교,P균<0.05;량조가입상동농도정산납세포활성비교,P균<0.05。수착정산납농도증가,량조조망단백c-PAPP、c-Caspase-3상대표체량축점승고,증식단백ERK、p-ERK상대표체량축점강저。여대조조동농도정산납비교,관찰조1、2、4、6 mmol/L정산납화순박c-PAPP、c-Caspase-3단백표체균승고,1、6 mmol/L정산납화순박ERK、p-ERK단백표체균강저;량조비교,P균<0.05。결론정산납연합순박가강저란소투명세포암ES-2세포활성,억제기증식、촉진기조망;정산납농도월고,상술작용월명현。
Objective To observe the effect of sodium butyrate combined with cisplatin on cell viability and prolifera -tion of ovarian clear cell carcinoma ES-2 cells.Methods The ovarian clear cell carcinoma ES-2 cells in the logarithmic phase were randomly divided into the observation groups and control groups .The observation groups were added 1, 2, 4 and 6 mmol/L sodium butyrate (NaB) and 5 μg/mL cisplatin.The control groups were added the same concentrations of NaB.The cell activities were detected by MMT , and the relative expression levels of c-PAPP, c-Caspase-3, ERK and p-ERK were detected by Western blotting .Results The cell viabilities of the observation groups which were treated with 1, 2, 4, 6 mmol/L NaB and 5 μg/mL cisplatin were 51%±3%, 39%±2%, 22%±2% and 11%±1%, respectively;and significant difference was found between groups (all P<0.05).The cell viabilities of the control groups were 88%± 4%, 76%±3%, 69%±2%and 54%±2%, respectively;and significant difference was found between groups ( all P<0.05).Meanwhile, significant difference was found in the cell viability between the two groups which were added with the same concentrations of NaB (all P<0.05).With the increased concentrations of NaB , the relative expression levels of c-PAPP and c-Caspase-3 in the two kinds of groups were gradually increased , and the levels of ERK and p-ERK were signifi-cantly decreased .Compared with the control groups , the relative expression levels of c-PAPP and c-Caspase-3 in the obser-vation groups which were added 1, 2, 4 and 6 mmol/L NaB and 5 μg/mL cisplatin were all increased and the levels of ERK and P-ERK were decreased in the observation groups which were added 1 and 6 mmol/L NaB and 5μg/mL cisplatin. Significant difference was found between the two kinds of groups (all P<0.05).Conclusion NaB combined with cispla-tin may decrease the cell viability of ovarian clear cell carcinoma ES-2 cells, inhibit the proliferation and promote the apop-tosis.The effect can be stronger with the higher concentrations of NaB .