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核因子-κB和IκB激酶作为癌症治疗靶点

NF-kappaB and IKK as therapeutic targets in cancer.

作者信息

Kim H J, Hawke N, Baldwin A S

机构信息

Department of Surgery, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.

出版信息

Cell Death Differ. 2006 May;13(5):738-47. doi: 10.1038/sj.cdd.4401877.

Abstract

The transcription factor NF-kappaB and associated regulatory factors (including IkappaB kinase subunits and the IkappaB family member Bcl-3) are strongly implicated in a variety of hematologic and solid tumor malignancies. A role for NF-kappaB in cancer cells appears to involve regulation of cell proliferation, control of apoptosis, promotion of angiogenesis, and stimulation of invasion/metastasis. Consistent with a role for NF-kappaB in oncogenesis are observations that inhibition of NF-kappaB alone or in combination with cancer therapies leads to tumor cell death or growth inhibition. However, other experimental data indicate that NF-kappaB can play a tumor suppressor role in certain settings and that it can be important in promoting an apoptotic signal downstream of certain cancer therapy regimens. In order to appropriately move NF-kappaB inhibitors in the clinic, thorough approaches must be initiated to determine the molecular mechanisms that dictate the complexity of oncologic and therapeutic outcomes that are controlled by NF-kappaB.

摘要

转录因子NF-κB及相关调节因子(包括IκB激酶亚基和IκB家族成员Bcl-3)与多种血液系统和实体肿瘤密切相关。NF-κB在癌细胞中的作用似乎涉及细胞增殖的调节、细胞凋亡的控制、血管生成的促进以及侵袭/转移的刺激。与NF-κB在肿瘤发生中的作用一致的是,单独抑制NF-κB或与癌症治疗联合使用会导致肿瘤细胞死亡或生长抑制。然而,其他实验数据表明,NF-κB在某些情况下可以发挥肿瘤抑制作用,并且在促进某些癌症治疗方案下游的凋亡信号方面可能很重要。为了在临床上合理应用NF-κB抑制剂,必须采取全面的方法来确定决定由NF-κB控制的肿瘤学和治疗结果复杂性的分子机制。

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