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作 者:贾喜花[1] 唐汉钧[2] 赵连臣[1] 耿淑美[1]
机构地区:[1]保定市第一中心医院,河北保定071000 [2]上海中医药大学附属龙华医院,200032
出 处:《临床误诊误治》2006年第6期10-11,共2页Clinical Misdiagnosis & Mistherapy
摘 要:目的:研究乳宁Ⅱ号对津白Ⅱ号(TA2)MA891小鼠乳腺癌的抑瘤和抗转移作用。方法:将体外培养的MA891细胞接种在津白Ⅱ号小鼠右腋皮下,接种后将小鼠分为生理盐水(NS)组、环磷酰胺(CTX)组、乳宁Ⅱ号组和CTX+乳宁Ⅱ号组。观察肿瘤抑制率和肺转移率、各组肿瘤细胞周期和凋亡情况。结果:CTX组、乳宁Ⅱ号组、CTX+乳宁Ⅱ号组与NS组比较均能显著抑制肿瘤和肺转移,抑瘤率分别为72.14%、35.1%、73.90%;肺转移抑制率分别为38.03%、34.04%、56.91%。结论:乳宁Ⅱ号能明显抑制肿瘤生长和抗转移,且对CTX有减毒增效的作用。Objective:To investigate antineoplastie and antimctastasizing effects of Runing Ⅱ prescription on Jinbai Ⅱ (TA2)mouse breast cancer line MA891. Methods:In vitro culture MA891 cells were inoculated subcutanously into Jinbai Ⅱ mice (TA2). And then the mice were divided into four groups and treated respectively with normal saline,cyclophosphamide (CTX) ,Runlng Ⅱ and cyclophosphamide(CTX) plus Runing Ⅱ. The growth of tumors and lung metastasis were observed and compared among the four groups. Results:Tumor inhibition rates were 72.14% .35.1%,73.90% in CTX group.Runing Ⅱ group and CTX + Runing Ⅱ group, respectively;the inhibition rates of lung metastases were 38.03% ,34.04% ,56.91% , respectively. Conclusion: Runing Ⅱ prescription could inhibit the growth of the tumor and reduce the lung metastases. And it could also reduce the toxicity of CTX abd enhance its therapeutic effectiveness.
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