Zhang Junfeng, Zhang Yunsheng, Cheng Lin, Li Chunlei, Dai Lei, Zhang Hui, Yan Fenglian, Shi Hui, Dong Guanjun, Ning Zhaochen, Xu Wei, Si Chuanping, Deng Hongxin, Xiong Huabao
Institute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong, China.
State Key Laboratory of Biotherapy/Collaborative Innovation Center for Biotherapy, West China Hospital, Sichuan University Chengdu, Sichuan, China.
Am J Transl Res. 2018 May 15;10(5):1552-1561. eCollection 2018.
Cancer stem cells (CSCs) play important roles in tumor initiation, metastasis, and progression. They are also mainly responsible for high treatment failure rates. Identification and characterization of CSCs are crucial for facilitating the detection, prevention, or therapy of cancer. Great efforts have been paid to develop an effective method and the ideal method for CSCs research is still in the going. In our study, we created an ultra-low concentration of serum and non-adhesive (ULCSN) culture system to enrich CSCs from murine lewis lung cancer cell line LL/2 with cell spheres structure and characterize the LL/2 CSCs properties. Their characteristics were investigated through colony formation, spheres formation, chemoresistance, flow cytometry for putative stem cell markers, such as CD133, CD34 and CD45, immunofluorescence staining and tumor initiation capacity . Tumor spheres were formed within 7-10 days under the condition of ULCSN culture system. Compared with adherent parental LL/2 cells, the colony capacity, chemo-resistance, and expression of stem cell markers increased significantly in addition to tumor-initiating capability in the tumor sphere cells. Using the ULCSN culture system, an available isolation method of lewis lung CSCs was established, which is simple, effective, and inexpensive compared with the cytokines attachment serum free culture method. The stem cell properties of the tumor sphere LL/2 cells reflected the CSCs phenotypes. We developed a useful CSCs model for basic and pre-clinical studies for lung cancer and other types of cancer.
癌症干细胞(CSCs)在肿瘤的起始、转移和进展中发挥着重要作用。它们也是导致高治疗失败率的主要原因。癌症干细胞的识别和表征对于促进癌症的检测、预防或治疗至关重要。人们已经付出巨大努力来开发一种有效的方法,而用于癌症干细胞研究的理想方法仍在探索之中。在我们的研究中,我们创建了一种超低血清浓度和非黏附(ULCSN)培养系统,以从具有细胞球结构的小鼠刘易斯肺癌细胞系LL/2中富集癌症干细胞,并表征LL/2癌症干细胞的特性。通过集落形成、球状体形成、化学抗性、针对假定干细胞标志物(如CD133、CD34和CD45)的流式细胞术、免疫荧光染色和肿瘤起始能力来研究它们的特性。在ULCSN培养系统条件下,7 - 10天内形成了肿瘤球。与贴壁的亲本LL/2细胞相比,肿瘤球细胞除了具有肿瘤起始能力外,其集落形成能力、化学抗性和干细胞标志物的表达也显著增加。利用ULCSN培养系统,建立了一种可行的刘易斯肺癌癌症干细胞分离方法,与细胞因子附着无血清培养方法相比,该方法简单、有效且成本低廉。肿瘤球LL/2细胞的干细胞特性反映了癌症干细胞的表型。我们为肺癌和其他类型癌症的基础研究和临床前研究开发了一种有用的癌症干细胞模型。