Characterization of cancer stem-like cells in chordoma Laboratory investigation

被引:50
作者
Aydemir, Esra [3 ]
Bayrak, Omer Faruk [2 ,3 ]
Sahin, Fikrettin [3 ]
Atalay, Basar [1 ]
Kose, Gamze Torun [3 ]
Ozen, Mustafa [2 ,5 ]
Sevli, Serhat [2 ]
Dalan, Altay Burak [4 ]
Yalvac, Mehmet Emir [3 ]
Dogruluk, Turgut [5 ]
Ture, Ugur [1 ]
机构
[1] Yeditepe Univ, Sch Med, Dept Neurosurg, TR-34752 Istanbul, Turkey
[2] Yeditepe Univ, Sch Med, Dept Med Genet, TR-34752 Istanbul, Turkey
[3] Yeditepe Univ, Fac Engn & Architecture, Dept Genet & Bioengn, TR-34752 Istanbul, Turkey
[4] Istanbul Univ, Inst Expt Med, Dept Mol Med, Istanbul, Turkey
[5] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
chordoma; cancer stem-like cell; differentiation; retinoic acid; SSEA-1; nucleus pulposus; oncology; SKULL BASE CHORDOMAS; TERM-FOLLOW-UP; RETINOIC ACID; PROSPECTIVE IDENTIFICATION; PROGENITOR CELLS; IN-VITRO; DIFFERENTIATION; MANAGEMENT; MARKER; GROWTH;
D O I
10.3171/2011.12.JNS11430
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Chordomas are locally aggressive bone tumors known to arise from the remnants of the notochord. Because chordomas are rare, molecular studies aimed at developing new therapies are scarce and new approaches are needed. Chordoma cells and cancer stem-like cells share similar characteristics, including self-renewal, differentiation, and resistance to chemotherapy. Therefore, it seems possible that chordomas might contain a subpopulation of cancer stem-like cells. The aim of this study is to determine whether cancer stem-like cells might be present in chordomas. Methods. In this study, the authors used gene expression analysis for common cancer stem-like cellmarkers, including c-myc, SSEA-I, oct4, klf4, sox2, nanog, and brachyury, and compared chordoma cells and tissues with nucleus pulposus tissues (disc degenerated nontumorigenic tissues). Differentiation through agents such as all-trans retinoic acid and osteogenic differentiation medium was induced to the chordoma cells. Additionally, U-CH I cells were sorted via magnetic cell sorting for stem cell markers CD133 and CD15. After separation, positive and negative cells for these markers were grown in a nonadherent environment, soft agar, to determine whether the presence of these cancer stem-like cells might be responsible for initiating chordoma. The results were compared with those of untreated cells in terms of migration, proliferation, and gene expression by using reverse transcriptase polymerase chain reaction. Results. The results indicate that chordoma cells might be differentiating and committing into an osteogenic lineage when induced with the osteogenic differentiation agent. Chordoma cells that are induced with retinoic acid showed slower migration and proliferation rates when compared with the untreated cells. Chordoma cells that were found to be enriched by cancer stem-like cell markers, namely CD133 and CD15, were able to live in a nonadherent soft agar medium, demonstrating a self-renewal capability. To the authors' knowledge, this is the first time that cancer stem-like cell markers were also found to be expressed in chordoma cells and tissues. Conclusions. Cancer stem-like cell detection might be an important step in determining the recurrent and metastatic characteristics of chordoma. This finding may lead to the development of new approaches toward treatments of chordomas. (http://thejns.org/doi/abs/10.3171/2011.12.JNS11430)
引用
收藏
页码:810 / 820
页数:11
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