Isolation and identification of cancer stem cells from primary human ovarian cancer tissues.
- Author:
Sheng LIN
1
;
Hai-xia LONG
;
Tong XIANG
;
Bo ZHU
;
Rong-kai XIE
Author Information
- Publication Type:Journal Article
- MeSH: AC133 Antigen; Animals; Antigens, CD; metabolism; Cell Differentiation; Cell Separation; methods; Female; Flow Cytometry; methods; Glycoproteins; metabolism; Humans; Immunomagnetic Separation; methods; Mice; Mice, Inbred NOD; Mice, SCID; Neoplasm Transplantation; Neoplastic Stem Cells; metabolism; pathology; Ovarian Neoplasms; metabolism; pathology; Peptides; metabolism
- From: Chinese Journal of Oncology 2011;33(12):896-899
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo isolate and identify the cancer stem cells from primary human ovarian cancer tissues.
METHODSFresh tumor tissues from five cases of pathologically diagnosed ovarian cancers were taken, minced and then digested with collagenase and hyaluronidase to obtain single cell suspension. The erythrocytes were removed with ACK Lysis buffer. The suspensions were sorted by magnetic activated cell sorting (MACS) using CD133-binding microbeads. Then the sorted CD133(+) cells were verified by flow cytometry. The cells were cultured in serum-free medium supplemented with EGF, bFGF, insulin and BSA, and grew into spheroids. Immunofluorescence, differentiation and tumor formation tests of the cells were performed to characterize the properties of cancer stem cells.
RESULTSThe ovarian cancer stem cells were successfully isolated from primary human ovarian tumors, which formed typical spheroids in serum-free medium and had stronger ability of tumorigenesis. The results of related experiments verified that CD133 positive cells owned the properties of cancer stem cells.
CONCLUSIONSThe ovarian cancer stem cells presenting the characteristics of stemness in vitro and in vivo, have been successfully isolated from primary human ovarian tumor tissues by MACS. The isolated ovarian cancer stem cells could be used in future researches of their biological functions.