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前列腺癌干细胞:新疗法的靶点。

Prostate cancer stem cells: a target for new therapies.

作者信息

Maitland N J, Bryce S D, Stower M J, Collins A T

机构信息

Department of Biology, YCR Cancer Research Unit, University of York, YO10 5YW York, UK.

出版信息

Ernst Schering Found Symp Proc. 2006(5):155-79. doi: 10.1007/2789_2007_050.

Abstract

Prostate cancer is now a common disease in men over 50 years of age. Medical therapies for prostate cancer are based on discoveries from the mid-twentieth century, and in the long term are rarely curative. Most treatments are directed towards an androgen receptor-expressing, highly proliferative target cell, which does indeed form the vast majority of cells in a prostate tumour. However, by invoking the existence of a cancer stem cell which, like normal epithelial stem cells in the prostate, does not express androgen receptor and is relatively quiescent, the observed resistance to most medical therapies can be explained. The phenotype of the prostate cancer stem cells is that of a basal cell and cultures derived from cancers, but not benign tissues, express a range of prostate cancer-associated RNAs. Furthermore, stem cells purified on the basis of alpha2beta1 high integrin and CD133 cell surface antigen expression, from an established culture of Gleason 4 (2+2) prostate cancer (P4E6), were able to form multiple intraprostatic tumours in nude mice when grafted orthotopically in a matrigel plug containing human prostatic stroma. The final tumours reexpressed androgen receptor and displayed a histology similar to that of a Gleason 4 cancer.

摘要

前列腺癌如今是50岁以上男性中的常见疾病。前列腺癌的医学疗法基于20世纪中叶的发现,从长远来看很少能治愈。大多数治疗针对表达雄激素受体、高度增殖的靶细胞,而这确实构成了前列腺肿瘤中绝大多数细胞。然而,通过提出癌症干细胞的存在,就像前列腺中的正常上皮干细胞一样,不表达雄激素受体且相对静止,就可以解释观察到的对大多数医学疗法的抗性。前列腺癌干细胞的表型是基底细胞的表型,源自癌症而非良性组织的培养物表达一系列前列腺癌相关RNA。此外,从已建立的Gleason 4(2+2)前列腺癌(P4E6)培养物中,基于α2β1高整合素和CD133细胞表面抗原表达纯化的干细胞,当原位移植到含有人类前列腺基质的基质胶塞中时,能够在裸鼠体内形成多个前列腺内肿瘤。最终的肿瘤重新表达雄激素受体,并显示出与Gleason 4癌症相似的组织学特征。

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