TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia

被引:38
作者
Bresin, A. [1 ]
D'Abundo, L. [2 ]
Narducci, M. G. [1 ]
Fiorenza, M. T. [3 ]
Croce, C. M. [4 ,5 ]
Negrini, M. [2 ]
Russo, G. [1 ]
机构
[1] IRCCS, IDI, Lab Oncol Mol, Via Monti Creta 104, I-00167 Rome, Italy
[2] Univ Ferrara, Dipartimento Morfol Chirurg & Med Sperimentale, Via Luigi Borsari 46, I-44121 Ferrara, Italy
[3] Univ Roma La Sapienza, Dipartimento Psicol, Sez Neurosci, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[4] Ohio State Univ, Human Canc Genet Program, OSU Sch Med, Columbus, OH 43210 USA
[5] Ohio State Univ, OSU Sch Med, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
关键词
ENDOPLASMIC-RETICULUM STRESS; T-CELL; LYMPHOID MALIGNANCIES; DISEASE PROGRESSION; INDUCE APOPTOSIS; MURINE MODEL; CLL; EXPRESSION; MICE; RECEPTOR;
D O I
10.1038/cddis.2015.419
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic lymphocytic leukemia (CLL) is a B-cell malignancy with a mature phenotype. In spite of its relatively indolent nature, no radical cure is as yet available. CLL is not associated with either a unique cytogenetic or a molecular defect, which might have been a potential therapeutic target. Instead, several factors are involved in disease development, such as environmental signals which interact with genetic abnormalities to promote survival, proliferation and an immune surveillance escape. Among these, PI3-Kinase signal pathway alterations are nowadays considered to be clearly important. The TCL1 gene, an AKT co-activator, is the cause of a mature T-cell leukemia, as well as being highly expressed in all B-CLL. A TCL1 transgenic mouse which reproduces leukemia with a distinct immunophenotype and similar to the course of the human B-CLL was developed several years ago and is widely used by many groups. This is a review of the CLL biology arising from work of many independent investigators who have used TCL1 transgenic mouse model focusing on pathogenetic, microenviroment and therapeutic targets.
引用
收藏
页码:e2071 / e2071
页数:11
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