Research Papers:
Enrichment of human osteosarcoma stem cells based on hTERT transcriptional activity
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Abstract
Ling Yu1,2, Shiqing Liu1, Chun Zhang1, Bo Zhang1, Bruno M. Simões2, Rachel Eyre2, Yi Liang3, Huichao Yan4, Zheng Wu5, Weichun Guo1, Robert B. Clarke2
1 Department of Orthopedics, Renmin Hospital of Wuhan University, Jiefang Road, Wuhan, Hubei, P.R. China
2 Institute of Cancer Sciences, University of Manchester, Wilmslow Road, Manchester, UK
3 State Key Laboratory of Oncology in Southern China and the Department of Experimental Research, Sun Yat-Sen University Cancer Center, Dongfeng Road, Guangzhou, Guangdong, P.R. China
4 Opening Laboratory for Oversea Scientists, Wuhan University School of Basic Medical Science, Donghu Road, Wuhan, Hubei, P.R. China
5 Department of Radiation Oncology, Tumor Hospital Xiangya School of Medicine of Central South University, Tongzipo Road, Changsha, Hunan, P.R.China
Correspondence:
Robert B Clarke, email:
Correspondence:
Shiqing Liu, email:
Keywords: Osteosarcoma; Heterogeneity; Cancer stem cells; Telomerase; Metastasis; Drug resistance
Received: October 30, 2013 Accepted: November 3, 2013 Published: November 5, 2013
Abstract
Telomerase is crucial for the maintenance of stem/progenitor cells in adult tissues and is detected in most malignant cancers, including osteosarcoma. However, the relationship between telomerase expression and cancer stem cells remains unknown. We observed that sphere-derived osteosarcoma cells had higher telomerase activity, indicating that telomerase activity might be enriched in osteosarcoma stem cells. We sorted subpopulations with high or low telomerase activity (TEL) using hTERT transcriptional promoter-induced green fluorescent protein (GFP). The TELpos cells showed an increased sphere and tumor propagating capacity compared to TELneg cells, and enhanced stem cell-like properties such as invasiveness, metastatic activity and resistance to chemotherapeutic agents both in vitro and in vivo. Furthermore, the telomerase inhibitor MST312 prevented tumorigenic potential both in vitro and in vivo, preferentially targeting the TELpos cells. These data support telomerase inhibition as a potential targeted therapy for osteosarcoma stem-like cells.
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