Expression of the Tpl2/Cot oncogene in human T-cell neoplasias

被引:40
作者
Christoforidou, Anna V. [1 ,2 ,3 ,4 ]
Papadaki, Helen A. [3 ,4 ]
Margioris, Andrew N. [1 ,2 ]
Eliopoulos, George D. [3 ,4 ]
Tsatsanis, Christos [1 ,2 ]
机构
[1] Univ Crete, Sch Med, Dept Clin Chem Biochem, Iraklion 71110, Crete, Greece
[2] Univ Hosp Herakl, Iraklion 71110, Crete, Greece
[3] Univ Crete, Sch Med, Dept Hematol, Iraklion 71110, Crete, Greece
[4] Univ Hosp Heracl, Iraklion 71110, Crete, Greece
关键词
D O I
10.1186/1476-4598-3-34
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Tpl2/Cot oncogene has been identified in murine T-cell lymphomas as a target of MoMuLV insertion. Animal and tissue culture studies have shown that Tpl2/Cot is involved in interleukin-2 (IL-2) and tumor necrosis factor-alpha (TNF-alpha) production by T-cells contributing to T-cell proliferation. In the present report we examined a series of 12 adult patients with various T-cell malignancies, all with predominant leukemic expression in the periphery, for the expression of Tpl2/Cot oncogene in order to determine a possible involvement of Tpl2/Cot in the pathogenesis of these neoplasms. Results: Our results showed that Tpl2/Cot was overexpressed in all four patients with Large Granular Lymphocyte proliferative disorders (LGL-PDs) but in none of the remaining eight patients with other T-cell neoplasias. Interestingly, three of the LGL-PD patients displayed neutropenia, one in association with sarcoidosis. Serum TNF-alpha levels were increased in all Tpl2/Cot overexpressing patients while serum IL-2 was undetectable in all subjects studied. Genomic DNA analysis revealed no DNA amplification at the Tpl2/Cot locus in any of the samples analyzed. Conclusions: We conclude that Tpl2/Cot, a gene extensively studied in animal and tissue culture T-cell models may be also involved in the development of human LGL-PD and may have a role in the pathogenesis of immune manifestations associated with these diseases. This is the first report implicating Tpl2/Cot in human T-cell neoplasias and provides a novel molecular event in the development of LGL-PDs.
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页数:9
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