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Identification of human brain tumour initiating cells

机译:人脑肿瘤起始细胞的鉴定

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The cancer stem cell (CSC) hypothesis suggests that neoplastic clones are maintained exclusively by a rare fraction of cells with stem cell properties(1,2). Although the existence of CSCs in human leukaemia is established(3,4), little evidence exists for CSCs in solid tumours, except for breast cancer(5). Recently, we prospectively isolated a CD133(+) cell subpopulation from human brain tumours that exhibited stem cell properties in vitro(6). However, the true measures of CSCs are their capacity for self renewal and exact recapitulation of the original tumour(1,2,7). Here we report the development of a xenograft assay that identified human brain tumour initiating cells that initiate tumours in vivo. Only the CD133(+) brain tumour fraction contains cells that are capable of tumour initiation in NOD-SCID (non-obese diabetic, severe combined immunodeficient) mouse brains. Injection of as few as 100 CD133(+) cells produced a tumour that could be serially transplanted and was a phenocopy of the patient's original tumour, whereas injection of 10 5 CD133(-) cells engrafted but did not cause a tumour. Thus, the identification of brain tumour initiating cells provides insights into human brain tumour pathogenesis, giving strong support for the CSC hypothesis as the basis for many solid tumours(5), and establishes a previously unidentified cellular target for more effective cancer therapies.
机译:癌症干细胞(CSC)假说表明,肿瘤克隆仅由稀有部分具有干细胞特性的细胞维持(1,2)。尽管已经建立了人类白血病中CSC的存在(3,4),但除了乳腺癌(5)以外,几乎没有证据表明实体瘤中存在CSC。最近,我们前瞻性地从人脑肿瘤中分离了CD133(+)细胞亚群,该亚群在体外表现出干细胞特性(6)。然而,CSCs的真正衡量标准是它们具有自我更新的能力以及对原始肿瘤的准确概括(1,2,7)。在这里,我们报告异种移植测定法的发展,该鉴定物鉴定了在体内引发肿瘤的人脑肿瘤引发细胞。只有CD133(+)脑肿瘤部分包含能够在NOD-SCID(非肥胖糖尿病,严重的联合免疫缺陷)小鼠大脑中引发肿瘤的细胞。注射少至100个CD133(+)细胞产生的肿瘤可以连续移植,是患者原始肿瘤的表型,而注射10 5个CD133(-)细胞则被植入但没有引起肿瘤。因此,脑肿瘤起始细胞的鉴定为人类脑肿瘤的发病机理提供了见识,为许多实体瘤的基础CSC假说提供了有力的支持(5),并为更有效的癌症治疗方法建立了以前未鉴定的细胞靶标。

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