Hypoxia-Regulated Delta-like 1 Homologue Enhances Cancer Cell Stemness and Tumorigenicity

被引:99
作者
Kim, Yuri [1 ]
Lin, Qun [1 ]
Zelterman, Daniel [2 ]
Yun, Zhong [1 ]
机构
[1] Yale Univ, Dept Therapeut Radiol, Sch Med, New Haven, CT 06520 USA
[2] Yale Univ, Dept Epidemiol & Publ Hlth, Sch Med, New Haven, CT 06520 USA
关键词
GENE-EXPRESSION; NEGATIVE CORRELATION; NEUROBLASTOMA-CELLS; ENDOCRINE TUMORS; GROWTH; DIFFERENTIATION; HIF-2-ALPHA; PHENOTYPE; LINES; FETAL;
D O I
10.1158/0008-5472.CAN-09-1605
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reduced oxygenation, or hypoxia, inhibits differentiation and facilitates stem cell maintenance. Hypoxia commonly occurs in solid tumors and promotes malignant progression. Hypoxic tumors are aggressive and exhibit stem cell-like characteristics. It remains unclear, however, whether and how hypoxia regulates cancer cell differentiation and maintains cancer cell stemness. Here, we show that hypoxia increases the expression of the stem cell gene DLK1, or delta-like 1 homologue (Drosophila), in neuronal tumor cells. Inhibition of DLK1 enhances spontaneous differentiation, decreases clonogenicity, and reduces in vivo tumor growth. Overexpression of DLK1 inhibits differentiation and enhances tumorigenic potentials. We further show that the DLK1 cytoplasmic domain, especially Tyrosine339 and Serine355, is required for maintaining both clonogenicity and tumorigenicity. Because elevated DLK1 expression is found in many tumor types, our observations suggest that hypoxia and DLK1 may constitute an important stem cell pathway for the regulation of cancer stem cell-like functionality and tumorigenicity. [Cancer Res 2009;69(24):9271-80]
引用
收藏
页码:9271 / 9280
页数:10
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