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基于细胞凋亡谱的弥漫性大 B 细胞淋巴瘤的分子靶向治疗。

Molecular targeted therapies for diffuse large B-cell lymphoma based on apoptosis profiles.

机构信息

Department of Clinical Pathology, VU University Medical Center, Amsterdam, The Netherlands.

出版信息

J Pathol. 2010 Apr;220(5):509-20. doi: 10.1002/path.2670.

Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common type of adult non-Hodgkin lymphoma and is treated with chemotherapy in combination with rituximab. Despite this aggressive therapy, the disease is fatal in 30-40% of patients. Inhibition of the apoptosis signalling pathways is strongly related to response to chemotherapy and eventual clinical outcome. In order to survive, lymphoma cells depend on disruption of the apoptosis pathway by mutations in apoptosis inducing genes or by continuous expression of anti-apoptotic proteins. The development of molecules targeting these apoptosis inhibitors provides a very promising opportunity to specifically target tumour cells without toxicity to non-malignant cells in DLBCL patients. Sensitivity for most of these antagonists can be predicted based on biological markers, suggesting the possibility of pre-defining patients who will most likely benefit from these targeted therapies. Experimental therapies aimed at restoring the upstream apoptosis pathway or targeting apoptosis inhibitors are currently being tested in clinical trials and are expected to be effective particularly in chemotherapy-refractory DLBCL, providing hope for patients who are refractory to current therapies.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)是最常见的成人非霍奇金淋巴瘤,采用化疗联合利妥昔单抗治疗。尽管采用了这种积极的治疗方法,但仍有 30-40%的患者死亡。凋亡信号通路的抑制与化疗反应和最终临床结果密切相关。为了生存,淋巴瘤细胞依赖于凋亡诱导基因的突变或持续表达抗凋亡蛋白来破坏凋亡途径。针对这些凋亡抑制剂的分子的开发为特异性靶向肿瘤细胞提供了一个非常有前途的机会,而不会对 DLBCL 患者的非恶性细胞产生毒性。大多数这些拮抗剂的敏感性可以基于生物标志物来预测,这表明有可能预先确定最有可能从这些靶向治疗中获益的患者。目前正在临床试验中测试旨在恢复上游凋亡途径或靶向凋亡抑制剂的实验疗法,预计在化疗耐药性 DLBCL 中特别有效,为对当前疗法耐药的患者带来希望。

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