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DLIA/Notch信号通路对乳腺癌化疗药物转运及化疗耐药性影响的实验研究

Experimental study of DLIA/Notch pathway function on chemoresistance and drug transporters in breast cancer
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摘要 目的探讨DLL4/Notch信号通路对乳腺癌药物转运及其对化疗耐药性影响。方法将24只雌性重症联合免疫缺陷小鼠完全随机分为观察组与对照组,每组12只,分别将BaF3-DLL4与BaF3.CK稳定转染乳腺癌细胞注射入观察组与对照组小鼠腋下成瘤,进行肿瘤血管体积系数与荧光灌注试验;选择形成肿瘤的裸鼠腹腔注射吉西他滨100mg/kg,比较2组的肿瘤血管体积系数、化疗药物灌注荧光率、血液灌注荧光率和吉西他滨治疗后2,3,4,5周肿瘤体积。结果观察组肿瘤血管体积系数(0.014±0.001)明显低于对照组(0.006±0.001),差异有统计学意义(P〈0.05)。观察组化疗药物灌注荧光率及血液灌注荧光率均明显低于对照组[(0.76±0.49)%比(1.34±0.45)%,(0.38±0.11)%比(0.64±0.22)%,均P〈0.05)。吉西他滨化疗治疗4、5周后对照组肿瘤体积大于观察组,对照组分别为(120±24)、(159±44)mm^3,观察组分别为(91±15)、(93±15)mm^3,差异有统计学意义(P〈0.05)。结论DLIA/Notch信号通路过度激活可引起乳腺癌血液灌注障碍,从而影响乳腺癌化疗药物转运,增强乳腺癌化疗耐药性。 Objective To investigate the chemoresistance and drug transporters of DLL4/Notch pathway in breast cancer. Methods Totally 24 female mice with severe combined immunodeficiency flat were equally divided into the observation group ( n = 6 ) and the control group ( n = 6 ). The BaF3-DLL4 and BaF3-CK cells were injected into the mice for tumor formation; the tumor vascular volume coefficient and fluorescent perfusion were tested; the formation tumors mice had gemcitabine. The tumor vascular volume coefficient, fluorescent chemotherapy infusion rate, blood perfusion fluorescence ratio and tumor volume between two groups were analyzed. Results The tumor vascular volume coefficient of the observation group was(0. 014 ±0. 001 ) , significantly lower than that in the control group (0. 006 ±0. 001 ) , ( P 〈 0.05 ). The chemotherapy infusion fluorescence rates and blood perfusion fluorescence rates in the observation group were significantly lower than those in control group [ ( 0.76 ± 0.49 ) % and ( 0.38± 0.11)% vs (1.34±0.45)% and (0.64 ±0.22)% , P〈0.05). After emcitabine chemotherapy for 4-5 weeks, the tumor volume in the control group and observation group was (120 ± 24), (159 ± 44) mm^3 vs (91± 15) , (93 ± 15) mm^3(p 〈0.05). Conclusions DLL4/Notch pathway excessive activation can induce blood perfusion disorder; it can affect chemotherapy drug transporters in the breast cancer to increase breast cancer chemotherapy drug resistance.
出处 《中国医药》 2015年第3期389-391,共3页 China Medicine
基金 湖北省教育厅科研项目(Q20132107)
关键词 DLL4/Notch信号通路 乳腺癌 化疗耐药性 药物转运 DLL4/Notch pathway Breast cancer Chemoresistance Drug transporters
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  • 1徐如祥,涂艳阳,姜晓丹,封江南,黄俊.小分子干扰RNA靶向抑制suvivin基因诱导U251细胞凋亡的实验研究[J].南方医科大学学报,2006,26(4):398-401. 被引量:3
  • 2成宇帆,王坚,周晓燕,周学科,陆永明,施达仁.荧光原位杂交检测石蜡包埋滑膜肉瘤组织中染色体易位的临床病理学意义[J].中华病理学杂志,2007,36(9):577-581. 被引量:11
  • 3Fernandez- Valdivia R, Takeuchi H, Samarghandi A, et al. Regulation of mammalian Notch signaling and embryonic development by the protein O-glucosyltransferase Rumi[J]. Development, 2011, 138( 10) :1925-1934.
  • 4Gianni-Barrera R, Trani M, Reginato S, et al. To sprout or to split VEGF, Notch and vascular morphogenesis [J]. Biochem Soc Trans, 2011, 39 (6) : 1644-1648.
  • 5Yalcin-Ozuysal O, Fiche M, Guitierrez M, et al. Antagonistic roles of Notch and p63 in controlling mammary epithelial cell fates [J]. Cell Death Differ, 2010, 17 (10) : 1600-1612.
  • 6Monahan P, Rybak S, Raetzman LT. The Notch target gene Hesl regulates cell cycle inhibitor expression in the developing pituitary [J]. Endocrinology, 2009, 150 (9) : 4386-4394.
  • 7Garcia A, Kandel JJ. Notch: a key regulator of tumor angiogenesis and metastasis [J]. Histol Histopathol, 2012, 27(2) :151-156.
  • 8Wang Z, Li Y, Banerjee S, et al. Down-regulation of Notch-1 and Jagged-I inhibits prostate cancer cell growth, migration and invasion, and induces apoptosis via inactivation of Akt, mTOR, and NF -KB signaling pathways [J]. J Cell Biochem, 2010, 109(4) :726-736.
  • 9Fortini ME. Notch signaling: the core pathway and its posttranslational regulation [J]. Dev Cell, 2009, 16 ( 5) : 633-647.
  • 10Ranganathan P, Weaver KL, Capobianco AJ ,et al. Notch signalling in solid tumours: a little bit of everything but not all the time [J]. Nat Rev Cancer, 2011, 11 ( 5 ) : 338- 351.

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