TY - JOUR
T1 - Implication of tumor stem-like cells in the tumorigenesis of sporadic paraganglioma
AU - Yang, Yueming
AU - Guo, Liandi
AU - Yang, Fan
AU - Huang, Qing
AU - Zhang, Fuping
AU - Ma, Hongwei
AU - Li, Hedong
AU - Yang, Kaixuan
AU - Lou, Jiangyan
AU - Liu, Cong
N1 - Funding Information:
Acknowledgments This work is supported by the Ministry of Science and Technology of China (2011CB966200 and 2013CB911000), National Natural Science Foundation of China (30970950), Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-10-0566), Program for Changjiang Scholars and Innovative Research Team in University of Ministry of Education of China (IRT0935), Department of Science and Technology of Sichuan Province (2011SZ0002 and 2012JQ0005), and Bureau of Science and Technology of Chengdu (11PPYB072SF).
PY - 2013/12
Y1 - 2013/12
N2 - It is commonly believed that paragangliomas are rare tumors arising from the neural crest-derived chromaffin cells. Although it has been speculated that paraganglioma is related to stem cell origin, there has been lack of direct evidence demonstrating the presence of (neural) stem cells in these tumor tissues. In this study, we found a subgroup of human paraganglioma from ten clinical samples displayed definitive markers of CD133 and/or nestin, the fundamental features of neural stem cell capable of self-renewal and differentiation. A panel of lineage-specific markers was also manifest in some of these tumors, consistent with the hierarchical and heterogeneous nature of these tumors. These observations strongly suggest that at least some forms of paraganglioma maintain tumor stem-like cells (TSCs) that potentially contribute to the histologic complexity of human paraganglioma. Finally, we found that the genomic DNA structure becomes highly unstable in tumor cells of paraganglioma, indicating the loss of tight control of genomic surveillance system be an important transitory event from normal multi-potent tissue stem cells to TSCs.
AB - It is commonly believed that paragangliomas are rare tumors arising from the neural crest-derived chromaffin cells. Although it has been speculated that paraganglioma is related to stem cell origin, there has been lack of direct evidence demonstrating the presence of (neural) stem cells in these tumor tissues. In this study, we found a subgroup of human paraganglioma from ten clinical samples displayed definitive markers of CD133 and/or nestin, the fundamental features of neural stem cell capable of self-renewal and differentiation. A panel of lineage-specific markers was also manifest in some of these tumors, consistent with the hierarchical and heterogeneous nature of these tumors. These observations strongly suggest that at least some forms of paraganglioma maintain tumor stem-like cells (TSCs) that potentially contribute to the histologic complexity of human paraganglioma. Finally, we found that the genomic DNA structure becomes highly unstable in tumor cells of paraganglioma, indicating the loss of tight control of genomic surveillance system be an important transitory event from normal multi-potent tissue stem cells to TSCs.
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U2 - 10.1007/s12032-013-0659-8
DO - 10.1007/s12032-013-0659-8
M3 - Article
C2 - 23996239
AN - SCOPUS:84883130266
SN - 1357-0560
VL - 30
JO - Medical Oncology
JF - Medical Oncology
IS - 4
M1 - 659
ER -