Department of Respiratory Medicine, The First Affiliated Hospital of Harbin Medical University, 23Youzheng Street, Nangang District, 150001 Harbin City, Heilongjiang, China.
Med Oncol. 2012 Jun;29(2):633-9. doi: 10.1007/s12032-011-9933-9. Epub 2011 Apr 12.
To investigate whether aldehyde dehydrogenase-1 (ALDH-1) in human lung cancer can be used as a sorting marker for stem cells in targeted therapies against human lung cancer. Spheres were induced by incubating cancer cells in a serum-free medium and formed with epidermal growth factor and fibroblast growth factor-10 (FGF10). Spheroid cells were combined with flow cytometry using the Aldefluor reagent to separate the SSCloALDEbr (ALDH-1-positive) cells. Cancer stem cells (CSCs) were characterized by their proliferation, colony formation, and tumorigenesis in nude mice and using phenotypic analysis. Float-growing spheres ("pulmospheres") were developed after SPC-A1 cells were cultured in a serum-free medium. The resultant sphere-forming cells included ALDH-1-positive cells as high as 15.13%. ALDH-1-positive CSCs have high proliferative ability, high cloning efficiency, and strong tumorigenicity. The rate of SSC(lo)ALDE(br) cell colony formation was 1.3-5.6%, whereas that of ALDE(-) cell colony formation was only 0-1.2% (P < 0.05). A cell count of only 1 × 10(3) SSC(lo)ALDE(br) cells was necessary to form tumors, whereas at least l × 10(5) ALDE(-) cells formed tumors. The same number of SSC(lo)ALDE(br) cells also formed larger tumors in a short latency period of tumor formation. The expression rates of CD133 in the SSC(lo)ALDE(br) and ALDE(-) cells were 16.31% (16.31 × 10(4)/10(6)) and 2.56% (2.56 × 10(4)/10(6)), respectively (P < 0.01). Moreover, the expression rates of ABCG2 in SSC(lo)ALDE(br) and ALDE(-) cells were 17.62% (17.62 × 10(4)/10(6)) and 3.45% (3.45 × 10(4)/10(6)), respectively (P < 0.01). Human lung adenocarcinoma bears CSCs, and ALDH-1 can act as a specific marker for human lung CSCs.
为了研究人肺癌中的醛脱氢酶-1(ALDH-1)是否可以用作针对人肺癌的靶向治疗中干细胞的分选标记物。通过在无血清培养基中孵育癌细胞来诱导球体,并与表皮生长因子和成纤维细胞生长因子-10(FGF10)一起形成。使用 Aldefluor 试剂结合流式细胞术将球体细胞与 ALDH-1 阳性细胞分离。通过在裸鼠中增殖、集落形成和肿瘤发生以及表型分析来鉴定癌症干细胞(CSC)。在无血清培养基中培养 SPC-A1 细胞后,会发展出漂浮生长的球体(“肺球体”)。形成的球体形成细胞中包含高达 15.13%的 ALDH-1 阳性细胞。ALDH-1 阳性 CSC 具有高增殖能力、高克隆效率和强致瘤性。SSC(lo)ALDE(br)细胞集落形成率为 1.3-5.6%,而 ALDE(-)细胞集落形成率仅为 0-1.2%(P <0.05)。仅需 1×10(3)个 SSC(lo)ALDE(br)细胞即可形成肿瘤,而至少需要 1×10(5)个 ALDE(-)细胞才能形成肿瘤。在肿瘤形成的潜伏期较短的情况下,相同数量的 SSC(lo)ALDE(br)细胞也形成更大的肿瘤。SSC(lo)ALDE(br)和 ALDE(-)细胞中 CD133 的表达率分别为 16.31%(16.31×10(4)/10(6))和 2.56%(2.56×10(4)/10(6))(P <0.01)。此外,SSC(lo)ALDE(br)和 ALDE(-)细胞中 ABCG2 的表达率分别为 17.62%(17.62×10(4)/10(6))和 3.45%(3.45×10(4)/10(6))(P <0.01)。人肺腺癌具有 CSC,并且 ALDH-1 可以作为人肺 CSC 的特异性标记物。