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基于高醛脱氢酶活性,在 OS99-1 细胞中前瞻性鉴定致瘤性骨肉瘤肿瘤干细胞。

Prospective identification of tumorigenic osteosarcoma cancer stem cells in OS99-1 cells based on high aldehyde dehydrogenase activity.

机构信息

Department of Neurosurgery, Spine Research Laboratory, University of Michigan Medical School, Ann Arbor, MI, USA.

出版信息

Int J Cancer. 2011 Jan 15;128(2):294-303. doi: 10.1002/ijc.25331. Epub 2010 Mar 22.

Abstract

High aldehyde dehydrogenase (ALDH) activity has recently been used to identify tumorigenic cell fractions in many cancer types. Herein we hypothesized that a subpopulation of cells with cancer stem cells (CSCs) properties could be identified in established human osteosarcoma cell lines based on high ALDH activity. We previously showed that a subpopulation of cells with high ALDH activity were present in 4 selected human osteosarcoma cell lines, of which a significantly higher ALDH activity was present in the OS99-1 cell line that was originally derived from a highly aggressive primary human osteosarcoma. Using a xenograft model in which OS99-1 cells were grown in NOD/SCID mice, we identified a highly tumorigenic subpopulation of osteosarcoma cells based on their high ALDH activity. Cells with high ALDH activity (ALDH(br) cells) from the OS99-1 xenografts were much less frequent, averaging 3% of the entire tumor population, compared to those isolated directly from the OS99-1 cell line. ALDH(br) cells from the xenograft were enriched with greater tumorigenicity compared to their counterparts with low ALDH activity (ALDH(lo) cells), generating new tumors with as few as 100 cells in vivo. The highly tumorigenic ALDH(br) cells illustrated the stem cell characteristics of self-renewal, the ability to produce differentiated progeny and increased expression of stem cell marker genes OCT3/4A, Nanog and Sox-2. The isolation of osteosarcoma CSCs by their high ALDH activity may provide new insight into the study of osteosarcoma-initiating cells and may potentially have therapeutic implications for human osteosarcoma.

摘要

高醛脱氢酶(ALDH)活性最近被用于鉴定许多癌症类型中的肿瘤发生细胞群。在这里,我们假设可以根据高 ALDH 活性鉴定出已建立的人骨肉瘤细胞系中的具有癌症干细胞(CSC)特性的细胞亚群。我们之前曾表明,在 4 种选定的人骨肉瘤细胞系中存在具有高 ALDH 活性的细胞亚群,其中 OS99-1 细胞系的 ALDH 活性明显更高,该细胞系最初源自高度侵袭性的原发性人骨肉瘤。我们使用 OS99-1 细胞在 NOD/SCID 小鼠中生长的异种移植模型,根据其高 ALDH 活性鉴定出具有高致瘤性的骨肉瘤细胞亚群。来自 OS99-1 异种移植的具有高 ALDH 活性的细胞(ALDH(br)细胞)要少得多,平均仅占整个肿瘤群体的 3%,而直接从 OS99-1 细胞系分离的细胞则要少得多。与低 ALDH 活性(ALDH(lo)细胞)的细胞相比,来自异种移植的 ALDH(br)细胞的致瘤性更高,能够在体内用少至 100 个细胞产生新的肿瘤。具有高致瘤性的 ALDH(br)细胞说明了自我更新、产生分化后代的能力以及干细胞标记基因 OCT3/4A、Nanog 和 Sox-2 的表达增加等干细胞特征。通过高 ALDH 活性分离骨肉瘤 CSC 可能为骨肉瘤起始细胞的研究提供新的见解,并可能对人类骨肉瘤具有潜在的治疗意义。

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