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Isolation and biological analysis of tumor stem cells from pancreatic adenocarcinoma

机译:胰腺腺癌肿瘤干细胞的分离与生物学分析

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摘要

AIM: To explore the method of isolation and biological analysis of tumor stem cells from pancreatic adenocarcinoma cell line PANC-1.METHODS: The PANC-1 cells were cultured in Dulbecco modified eagle medium F12 (1:1 volume) (DMEM-F12) supplemented with 20% fetal bovine serum (FBS). Subpopulation cells with properties of tumor stem cells were isolated from pancreatic adenocarcinoma cell line PANC-1 according to the cell surface markers CD44 and CD24 by flow cytometry. The proliferative capability of these cells in vitro were estimated by 3-[4,5-dimehyl-2-thiazolyl]-2, 5-diphenyl-2H-tetrazolium bromide (MTT) method. And the tumor growth of different subpopulation cells which were injected into the hypodermisof right and left armpit of nude mice was studied, and expression of CD44 and CD24 of the CD44+CD24+ cell-formed nodules and PANC-1 cells were detected by avidin-biotin-peroxidase complex (ABC) immunohistochemical staining.RESULTS: The 5.1%-17.5% of sorted PANC-1 cells expressed the cell surface marker CD44, 57.8% -70.1% expressed CD24, only 2.1%-3.5% of cells were CD44+ CD24+. Compared with CD44-CD24- cells, CD44+CD24+ cells had a lower growth rate in vitro. Implantation of 104 CD44-CD24- cells in nude mice showed no evident tumor growth at wk 12. In contrast, large tumors were found in nude mice implanted with 103 CD44+CD24+ cells at wk 4 (2/8), a 20-fold increase in tumorigenic potential (P < 0.05 or P < 0.01). There was no obvious histological difference between the cells of the CD44+CD24+ cell-formed nodules and PANC-1 cells.CONCLUSION: CD44 and CD24 may be used as the cell surface markers for isolation of pancreatic cancer stem cells from pancreatic adenocarcinoma cell line PANC-1. Subpopulation cells CD44+CD24+ have properties of tumor stem cells. Because cancer stem cells are thought to be responsible for tumor initiation and its recurrence after an initial response to chemotherapy, it may be a very promising target for new drug development.
机译:目的:探讨从胰腺腺癌细胞株PANC-1中分离和生物学分析肿瘤干细胞的方法。方法:在Dulbecco改良的Eagle F12培养基(1:1体积)(DMEM-F12)中培养PANC-1细胞。补充有20%的胎牛血清(FBS)。通过流式细胞术根据细胞表面标志物CD44和CD24从胰腺腺癌细胞系PANC-1中分离具有肿瘤干细胞特性的亚群细胞。这些细胞在体外的增殖能力通过3- [4,5-二甲基-2-噻唑基] -2、5-二苯基-2H-四唑溴化物(MTT)方法估算。并研究了裸鼠左右腋下皮下注射的不同亚群细胞的肿瘤生长,并研究了CD44 + CD24 + 的CD44和CD24表达亲和素-生物素-过氧化物酶复合物(ABC)免疫组织化学染色检测到细胞形成的结节和PANC-1细胞。结果:分选的PANC-1细胞中有5.1%-17.5%的细胞表面标志物CD44占57.8%-70.1%表达CD24的细胞中,只有2.1%-3.5%的细胞是CD44 + CD24 + 。与CD44 - CD24 -细胞相比,CD44 + CD24 + 细胞的体外生长速率较低。在裸鼠中植入10 4 CD44 - CD24 -细胞在第12周时没有明显的肿瘤生长。相反,在在第4周(2/8)植入10 3 CD44 + CD24 + 细胞的裸鼠,致瘤潜力增加了20倍( P <0.05或P <0.01)。 CD44 + CD24 + 细胞形成的结节与PANC-1细胞之间的组织学差异无统计学意义。结论:CD44和CD24可作为该细胞表面标志物,用于从胰腺腺癌细胞系PANC-1中分离胰腺癌干细胞。亚群细胞CD44 + CD24 + 具有肿瘤干细胞的特性。因为癌症干细胞被认为是导致肿瘤的发生及其对化学疗法的最初反应后复发的原因,所以它可能是新药开发的非常有希望的目标。

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