Clinical and biological implications of MYC activation: a common difference between MGUS and newly diagnosed multiple myeloma

被引:235
作者
Chng, W-J [1 ,2 ,3 ]
Huang, G. F. [2 ]
Chung, T. H. [3 ]
Ng, S. B. [4 ]
Gonzalez-Paz, N. [5 ]
Troska-Price, T. [5 ]
Mulligan, G. [6 ]
Chesi, M. [1 ]
Bergsagel, P. L. [1 ]
Fonseca, R. [1 ]
机构
[1] Mayo Clin, Ctr Comprehens Canc, Dept Haematol Oncol, Scottsdale, AZ USA
[2] Natl Univ Singapore, Natl Univ Hlth Syst, Natl Univ Canc Inst Singapore, Dept Haematol Oncol, Singapore 117548, Singapore
[3] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117548, Singapore
[4] Natl Univ Singapore, Dept Pathol, Singapore 117548, Singapore
[5] Mayo Clin, Dept Haematol, Rochester, MN USA
[6] Millennium Pharmaceut Inc, Translat Med, Boston, MA USA
基金
新加坡国家研究基金会;
关键词
myeloma; MYC; bortezomib; MGUS; hyperdiploid; NF-KAPPA-B; C-MYC; MONOCLONAL GAMMOPATHY; UNDETERMINED SIGNIFICANCE; BURKITTS-LYMPHOMA; PROTEIN STABILITY; GENETIC EVENTS; RAS MUTATIONS; CELL LYMPHOMA; EXPRESSION;
D O I
10.1038/leu.2011.53
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Events mediating transformation from the pre-malignant monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) are unknown. We analyzed gene expression data sets generated on the Affymetrix U133 platform from 22 MGUS and 101 MM patients using gene-set enrichment analysis. Genes overexpressed in MM were enriched for cell cycle, proliferation and MYC activation gene sets. Upon dissecting the relationship between MYC and cell-cycle gene sets, we identified and validated an MYC activation signature dissociated from proliferation. Applying this signature, MYC is activated in 67% of myeloma, but not in MGUS. This was further confirmed by immunohistochemistry (IHC) using membrane CD138 and nuclear MYC double staining. We also showed that almost all tumors with RAS mutations expressed the MYC activation signature, and multiple mechanisms may be involved in activating MYC. MYC activation, whether assessed by gene-expression signature or IHC, is associated with hyperdiploid MM and shorter survival even in tumors that are not proliferative. Bortezomib treatment is able to overcome the survival disadvantage in patients with MYC activation. Leukemia (2011) 25, 1026-1035; doi:10.1038/leu.2011.53; published online 5 April 2011
引用
收藏
页码:1026 / 1035
页数:10
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