Enrichment of cancer-initiating cells from colon cancer cells through porous polymeric membranes by a membrane filtration method

被引:7
作者
Sung, Tzu-Cheng [1 ,2 ]
Huang, Wei-Lun [1 ]
Ban, Lee-Kiat [3 ]
Lee, Henry Hsin-Chung [3 ,4 ]
Wang, Jia-Hua [1 ]
Su, Her-Young [5 ]
Jen, Shih Hsi [6 ]
Chang, Yen-Hsiang [7 ]
Yang, Jen-Ming [8 ]
Higuchi, Akon [1 ,2 ,9 ,10 ,11 ,12 ]
Ye, Qingsong [13 ,14 ,15 ,16 ]
机构
[1] Natl Cent Univ, Dept Chem & Mat Engn, 300 Jhongda Rd, Taoyuan 32001, Taiwan
[2] Wenzhou Med Univ, Eye Hosp, Sch Ophthalmol & Optometry, 270 Xueyuan Rd, Wenzhou 325027, Zhejiang, Peoples R China
[3] Hsinchu Cathay Gen Hosp, Dept Surg, 678,Sec 2,Zhonghua Rd, Hsinchu 30060, Taiwan
[4] Natl Cent Univ, Grad Inst Translat & Interdisciplinary Med, 300 Jhongda Rd, Taoyuan 32001, Taiwan
[5] Bobson Yuho Women & Childrens Clin, Dept Obstet & Gynecol, 182 Zhuangjing S Rd, Hsinchu 302, Taiwan
[6] Taiwan Landseed Hosp, Dept Obstet & Gynecol, 77 Kuangtai Rd, Taoyuan 32405, Taiwan
[7] Chang Gung Mem Hosp, Dept Gen Dent, Taoyuan 333, Taiwan
[8] Chang Gung Univ, Dept Chem & Mat Engn, Taoyuan 333, Taiwan
[9] Chung Yuan Christian Univ, Dept Chem Engn, Taoyuan 320, Taiwan
[10] Chung Yuan Christian Univ, R&D Ctr Membrane Technol, Taoyuan 320, Taiwan
[11] RIKEN, Ctr Emergent Matter Sci, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[12] Univ Chinese Acad Sci, Wenzhou Inst, 16 Xinsan Rd,Hitech Ind Pk, Wenzhou, Zhejiang, Peoples R China
[13] Wuhan Univ, Renmin Hosp, Ctr Regenerat Med, Wuhan 430060, Peoples R China
[14] Massachusetts Gen Hosp, Skeletal Biol Res Ctr, OMFS, Boston, MA 02114 USA
[15] Harvard Sch Dent Med, Boston, MA 02114 USA
[16] Wenzhou Med Univ, Sch & Hosp Stomatol, Wenzhou, Zhejiang, Peoples R China
关键词
STEM-CELLS; MARKER; DIFFERENTIATION; CD133; SCAFFOLDS; TISSUE; ASSAY; NANOPARTICLES; PLASTICITY; DELIVERY;
D O I
10.1039/d0tb02312d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Cancer-initiating cells (CICs) or cancer stem cells (CSCs) are primarily responsible for tumor initiation, growth, and metastasis and represent a few percent of the total tumor cell population. We designed a membrane filtration protocol to enrich CICs (CSCs) from the LoVo colon cancer cell line via nylon mesh filter membranes with 11 and 20 mu m pore sizes and poly(lactide-co-glycolic acid)/silk screen (PLGA/silk screen) porous membranes (pore sizes of 20-30 mu m). The colon cancer cell solution was filtered through the membranes to obtain a permeate solution. Subsequently, the cell culture medium was filtered through the membranes to collect the recovery solution where the cells attached to the membranes were rinsed off into the recovery solution. Then, the membranes were cultivated in the cultivation medium to collect the migrated cells from the membranes. The cells migrated from any membrane had higher expression of the CSC surface markers CD44 and CD133, had higher colony formation levels, and produced more carcinoembryonic antigen (CEA) than the colon cancer cells cultivated on conventional tissue culture plates (control). We established a method to enrich the CICs (CSCs) of colon cancer cells from migrated cells through porous polymeric membranes by the membrane filtration protocol developed in this study.
引用
收藏
页码:10577 / 10585
页数:9
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