SOCS1 is significantly up-regulated in Nutlin-3-treated p53wild-type B chronic lymphocytic leukemia (B-CLL) samples and shows an inverse correlation with miR-155

被引:14
作者
di Iasio, Maria Grazia [2 ,3 ]
Norcio, Alessia [2 ,3 ]
Melloni, Elisabetta [2 ,3 ]
Zauli, Giorgio [1 ]
机构
[1] IRCCS Burlo Garofolo Trieste, Inst Maternal & Child Hlth, I-34100 Trieste, Italy
[2] Univ Ferrara, Dept Morphol & Embryol, I-44100 Ferrara, Italy
[3] Univ Ferrara, LTTA Ctr, I-44100 Ferrara, Italy
关键词
Nutlin-3; Primary B-CLL; SOCS1; miRNA-155; ACUTE MYELOID-LEUKEMIA; T-CELLS; EXPRESSION; PATHWAY; METHYLATION; ACTIVATION; MICRORNA; PROTEIN; TRAIL;
D O I
10.1007/s10637-011-9786-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The basal SOCS1 mRNA levels were significantly lower in p53(mutated) BJAB and MAVER leukemic cell lines with respect to p53(wild-type) SKW6.4 and JVM-2 leukemic cell lines, p53(wild-type) primary B chronic lymphocytic leukemia (B-CLL) cells and primary normal peripheral blood mononuclear cells (PBMC). Moreover, the MDM2 small molecule inhibitor Nutlin-3 significantly increased the levels of SOCS1 mRNA in both primary p53(wild-type) B-CLL cells as well as in p53(wild-type) B leukemic cell lines, but not in p53(mutated) B leukemic cell lines nor in primary PBMC. Of note, a significant inverse correlation was observed between SOCS1 mRNA and miR-155 levels in Nutlin-3-treated primary B-CLL cells and PBMC, suggesting that the miRNA-155/SOCS1 axis represents a potentially important therapeutic target of Nutlin-3 in B-CLL.
引用
收藏
页码:2403 / 2406
页数:4
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