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雄激素剥夺治疗对前列腺癌癌干细胞的影响

The Effect of Androgen Deprivation Therapy on Prostate Cancer Stem Cells
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摘要 目的探讨雄激素剥夺治疗(ADT)对前列腺癌癌干细胞(PrCSC)比例及干细胞相关基因的影响。方法由雄激素依赖性前列腺癌细胞系LNCaP诱导出雄激素非依赖性前列腺癌细胞系LNCaPAI,流式细胞技术检测ADT对LNCaP中PrCSC比例以及雄激素对LNCaPAI中PrCSC比例的影响,Western blot及实时定量PCR检测BMI-1、ABCG2和NANOG的变化。结果由LNCaP诱导出LNCaPAI细胞,LNCaP细胞中PrCSC的比例为0.04%。ADT 4周后PrCSC的比例增加至0.23%,6个月后形成LNCaPAI时则达到0.74%。ADT 3周后,BMI-1、NANOG、ABCG2的表达逐渐增高,LNCaPAI中BMI-1、NANOG、ABCG2表达明显高于LNCaP。双氢睾酮作用于LNCaPAI后PrCSC的比例逐渐下降,第2周时下降至0.43%,第3周时下降至0.37%,第4周下降至0.33%。同时BMI-1、NANOG和ABCG2的表达逐渐降低。结论 ADT可以使LNCaP逐渐形成LNCaPAI,此时PrCSC比例增加,同时干细胞相关基因表达增加。双氢睾酮可以减少雄激素非依赖性前列腺癌中PrCSC比例。间断雄激素治疗可能是治疗前列腺癌的较好选择。 Objective To investigate the effect of androgen deprivation therapy(ADT) on ratio of prostate cancer stem cell(PrCSC) and the gene expression relative to stem cell.Methods An androgen-independent subline(LNCaPAI) was established by continuously culturing the LNCaP cells in the medium without androgen.After the LNCaP cells were ablated of androgen,the proportion of PrCSC were assessed by flow cytometry analysis and the expressions of BMI-1,ABCG2 and NANOG were assessed by Western blot and real-time RT-PCR.After cultured with androgen,the proportion of PrCSC and expression of BMI-1,ABCG2 and NANOG in LNCaPAI were assessed.Results The LNCaPAI subline were established from androgen-dependent LNCaP cells.In the LNCaP cell line,the CD44+/CD24-subpopulation(PrCSC) was rare(0.04%),whereas the LNCaPAI cell line had a more prevalent CD44+/CD24-population(0.74%).After the LNCaP cells were cultured in an androgen deprivation condition,the CD44+/CD24-subpopulation was increased.The expressions of BMI-1,ABCG2 and NANOG were increased after the LNCaP cells cultured in an androgen deprivation condition.The CD44+/CD24-subpopulation was significantly decreased when LNCaPAI cells were cultured with androgen.And the expressions of BMI-1,NANOG and ABCG2 were decreased,too.Conclusion It was found for the first time in our study that the CD44+/CD24-subpopulation was increased in androgen-dependent prostate cancer after androgen deprivation.We also found that the CD44+/CD24-subpopulation was decreased in LNCaPAI cells after androgen treatment.So the intermittent endocrinological treatments might be a good choice for the patients with prostate cancer.
出处 《中国医科大学学报》 CAS CSCD 北大核心 2011年第9期787-790,共4页 Journal of China Medical University
基金 中国博士后科学基金资助项目(20080431366)
关键词 前列腺癌 雄激素 癌干细胞 prostate cancer androgen cancer stem cell
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参考文献10

  • 1孙颖浩.我国前列腺癌的研究现状[J].中华泌尿外科杂志,2004,25(2):77-80. 被引量:355
  • 2Calabro F,Sternberg CN. Current indications for chemotherapy in prostate cancer patients[ J ]. Eur Urol, 2007,51 ( 1 ) : 17-26. 被引量:1
  • 3叶敏.前列腺癌的间歇雄激素阻断疗法(附编者按)[J].中华泌尿外科杂志,2001,22(2):116-118. 被引量:16
  • 4Bonnet D,Dick JE. Human acute leukaemia is organized as a hierarchy that originates from a primitive hemalopoietic cell[J].Nat Med, 1997,3 ( 7 ) : 730-737. 被引量:1
  • 5Tso CL, MeBride WH, Sun J, et al. Andrngen deprivation induces se leetive outgrowth of aggressive hormone-refractory prostate cancer clones expressing distinct cellular and molecular properties not present in parental androgen-dependent cancer cells [J]. Cancer J, 2000,6( 4 ) : 220-233. 被引量:1
  • 6Hurt EM,Kawasaki BT,Klarmann C,J,et al. CD44^+CD24^- prostate cells are early cancer progenitor/stem cells that provide a model for patients with poor prognosis[J]. Br J Cancer, 2008,98( 4 ) : 756 765. 被引量:1
  • 7Diehn M,Clarke MF. Cancer stem cells and radiothcrapy:new in sights into tumor radioresistance [J]. J Natl Caner Iost,2006,98 (24) : 1755-1757. 被引量:1
  • 8van Leenders GJ, Dukers D, Hessels D, et al. Polycomb-group oncogenes EZH2, BM11, and RING1 are overexpressed in prostate cancer with adverse pathologic and clinical features [ J ]. Eur Urol, 2007,52 ( 2 ) : 455-463. 被引量:1
  • 9Zhou S,Sehuetz JD,Bunting KD,et al. The ABC trausporter Berpl/ ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the sidepopulation phenotype [J ]. Nat Meal,2001,7 (9) : 1028-1034. 被引量:1
  • 10Wang SH,Tsai MS,Chiang MF,et al. A novel NK-type homeobox gene, ENK (early embryo specific NK), preferentially expressed in embryonic stem cells[ J ]. Gene Expr Patterns, 2003,3( 1 ): 99-103. 被引量:1

二级参考文献7

  • 1Gleave M E,Cancer Res,1992年,52卷,1598页 被引量:1
  • 2Hannun Y A,Blood,1997年,89卷,1845页 被引量:1
  • 3Theyer G,Br J Cancer,1997年,75卷,1515页 被引量:1
  • 4Parker S L,CA Cancer J Clin,1997年,47卷,5页 被引量:1
  • 5Von Eschenbach A,CA Cancer J Clin,1997年,47卷,261页 被引量:1
  • 6Bladou F,Int J Cancer,1996年,67卷,785页 被引量:1
  • 7Stoll B A,Eur J Cancer.A,1995年,31卷,2415页 被引量:1

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