Positioning of proteasome inhibitors in therapy of solid malignancies.

Positioning of proteasome inhibitors in therapy of solid malignancies.
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蛋白酶体抑制剂在固体恶性肿瘤治疗中的定位。

DOI:
10.1007/s00280-017-3489-0
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发表时间:
2018-03
影响因子:
3
通讯作者:
Jansen G
Jansen G
中科院分区:
医学3区
文献类型:
--
作者:
Roeten MSF;Cloos J;Jansen G

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靶向蛋白质降解途径,特别是泛素-蛋白酶体系统,已经成为一种有吸引力的新的癌症化疗方式。虽然蛋白酶体抑制剂在血液系统恶性肿瘤的治疗中得到了最成功的应用,但它们在实体肿瘤的治疗中也受到了持续的关注。本文综述了蛋白酶体抑制剂在治疗常见实体恶性肿瘤(如肺癌、结肠癌、胰腺癌、乳腺癌和头颈癌)中的定位,讨论了它们的作用机制(S)、预测因素和耐药的分子机制。
Targeting of the protein degradation pathway, in particular, the ubiquitin-proteasome system, has emerged as an attractive novel cancer chemotherapeutic modality. Although proteasome inhibitors have been most successfully applied in the treatment of hematological malignancies, they also received continuing interest for the treatment of solid tumors. In this review, we summarize the current positioning of proteasome inhibitors in the treatment of common solid malignancies (e.g., lung, colon, pancreas, breast, and head and neck cancer), addressing topics of their mechanism(s) of action, predictive factors and molecular mechanisms of resistance.
蛋白酶体抑制剂carfilzomib用伊立替康(Irinotecan)在肺癌和其他对先前治疗方面进展的伊诺特坎敏感性恶性肿瘤的1B试验(Onyx IST参考号:CAR-IST-553)。
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