Combination of low doses of Enzastaurin and Lenalidomide has synergistic activity in B-non-Hodgkin lymphoma cell lines

被引:9
作者
Cosenza, Maria [1 ]
Civallero, Monica [1 ]
Grisendi, Giulia [1 ]
Marcheselli, Luigi [1 ]
Roat, Erika [2 ]
Bari, Alessia [1 ]
Sacchi, Stefano [1 ]
机构
[1] Univ Modena & Reggio Emilia, Program Innovat Therapies Oncol & Haematol, Dept Hematol & Oncol, I-41124 Modena, Italy
[2] Univ Modena & Reggio Emilia, Dept Biomed Sci, I-41124 Modena, Italy
关键词
Indolent B-cell lymphoma; Enzastaurin; Lenalidomide; Signaling pathways; AKT; MAPK; C-BETA-INHIBITOR; MULTIPLE-MYELOMA; DRUG-RESISTANCE; AKT PATHWAY; PHASE-II; IN-VITRO; KINASE; APOPTOSIS; CANCER; PROLIFERATION;
D O I
10.1007/s00277-012-1490-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Less toxic and more active treatments are needed for indolent lymphomas as there is no curative treatment, and patients eventually die due to complications related to their disease. The purpose of the present study was to assess the antitumour activity of the combination of low doses of Enzastaurin and Lenalidomide (Revlimid) on B-lymphoma cell lines. The combination of Enzastaurin and Lenalidomide, at doses as low as 1 mu M, showed strong synergism against indolent lymphomas by reducing cell growth, producing an increase in G0-G1 phase followed by significant decrease in S phase, increasing apoptosis, and inhibiting PI3K/AKT, PKC and MAPK/ERK pathways. These preclinical findings, together with promising results obtained with Lenalidomide for the treatment of non-Hodgkin lymphoma, suggest that further evaluation of the combination of Enzastaurin and Lenalidomide for the treatment of indolent lymphomas is warranted. These compounds, with a favourable toxicity profile, are not classic chemotherapeutic agents, causing severe side effects, and could be considered an example of a new innovative attempt of an anti-cancer 'soft treatment'.
引用
收藏
页码:1613 / 1622
页数:10
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