An Yong, Yao Jie, Wei Ji-Shu, Lu Zi-Peng, Cai Hui-Hua, Dai Cun-Cai, Qian Zhu-Yin, Xu Ze-Kuan, Miao Yi
Department of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210009, China.
Zhonghua Wai Ke Za Zhi. 2010 Jul 1;48(13):999-1003.
To establish a gemcitabine-resistant pancreatic cancer cell line SW1990/GZ, and to explore the relationship between drug-resistant cell line SW1990/GZ and pancreatic cancer stem cell.
Gemcitabine-resistant pancreatic cancer cell line SW1990/GZ was obtained by treating parental cell line SW1990 in vitro with increasing dosage of gemcitabine in culture medium intermittently for 24 weeks. Stable cultures were obtained which were 77.2-fold increased in resistance relative to parental cells. Gene expressions of ABCB1/MDR1, ABCC1/MRP and ABCG2/BCRP were determined by real-time PCR. Tumorigenic potential was performed by nude mice xenograft transplant experiments. Side population analysis and CD24CD44 positive cells explore were determined by flow cytometry to examine cancer stem cell proportion.
Gemcitabine-resistant cell line SW1990/GZ underwent obvious morphological and functional changes. Compared with the parental cell line, SW1990/GZ cell was small and turned into round shape. SW1990/GZ had a higher gene expression level of ABCB1/MDR1, ABCC1/MRP and ABCG2/BCRP than SW1990 (P < 0.01). Nude mice xenograft transplant experiments showed that only 1 × 10(5) SW1990/GZ cells were sufficient for tumor formation, whereas an injection of 1 × 10(5) SW1990 cells did not initiate tumors. Flow cytometry analysis showed that SP proportion in SW1990/GZ was (11.0 ± 1.0)%, whereas in parental SW1990 it was (4.6 ± 0.9)%, CD44CD24 positive cells was (8.73 ± 0.81)% in SW1990/GZ, whereas (1.1 ± 0.4)% in SW1990.
Gemcitabine-resistant cell line SW1990/GZ has a higher proportion of pancreatic cancer stem cells compared to its parental cell line SW1990. CD44 is mainly responsible for acquired drug resistance, which can be a potential target to overcome acquired drug resistance in pancreatic cancer.
建立吉西他滨耐药的胰腺癌细胞系SW1990/GZ,并探讨耐药细胞系SW1990/GZ与胰腺癌干细胞之间的关系。
通过在培养基中用递增剂量的吉西他滨间歇处理亲代细胞系SW1990 24周,获得吉西他滨耐药的胰腺癌细胞系SW1990/GZ。获得稳定培养物,其耐药性相对于亲代细胞增加了77.2倍。通过实时PCR测定ABCB1/MDR1、ABCC1/MRP和ABCG2/BCRP的基因表达。通过裸鼠异种移植实验进行致瘤潜能研究。通过流式细胞术进行侧群分析和CD24CD44阳性细胞检测,以检查癌干细胞比例。
吉西他滨耐药细胞系SW1990/GZ发生了明显的形态和功能变化。与亲代细胞系相比,SW1990/GZ细胞变小并呈圆形。SW1990/GZ的ABCB1/MDR1、ABCC1/MRP和ABCG2/BCRP基因表达水平高于SW1990(P<0.01)。裸鼠异种移植实验表明,仅1×10⁵个SW1990/GZ细胞就足以形成肿瘤,而注射1×10⁵个SW1990细胞则不会引发肿瘤。流式细胞术分析显示,SW1990/GZ中的侧群比例为(11.0±1.0)%,而亲代SW1990中为(4.6±0.9)%;SW1990/GZ中CD44CD24阳性细胞为(8.73±0.81)%,而SW1990中为(1.1±0.4)%。
与亲代细胞系SW1990相比,吉西他滨耐药细胞系SW1990/GZ具有更高比例的胰腺癌干细胞。CD44主要负责获得性耐药,可作为克服胰腺癌获得性耐药的潜在靶点。