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实体瘤中的核因子κB

NF-kappaB in solid tumors.

作者信息

Pacifico Francesco, Leonardi Antonio

机构信息

Istituto di Endocrinologia e Oncologia Sperimentale, CNR, Italy.

出版信息

Biochem Pharmacol. 2006 Oct 30;72(9):1142-52. doi: 10.1016/j.bcp.2006.07.032. Epub 2006 Sep 7.

Abstract

Cancer is a multistep process during which cells acquire genetic alterations that drive the progressive transformation of normal cells into highly malignant cells. Self-sufficiency in growth, insensitivity to anti-growth signals, evasion of apoptosis, limitless replicative potential, sustained angiogenesis, tissue invasion and metastasis, are signatures of transformed cells. NF-kappaB is a key actor in tumorigenesis given its ability to control the expression and the function of a number of genes involved in these processes. Indeed, constitutive activation of NF-kappaB is a common feature of many human tumors, while its sustained activation during inflammation predisposes normal cells to neoplastic transformation. Since suppression of NF-kappaB has been shown to inhibit oncogenic potential of transformed cells, targeting it should be effective in the prevention and treatment of cancer.

摘要

癌症是一个多步骤过程,在此过程中细胞获得基因改变,促使正常细胞逐步转变为高度恶性的细胞。生长自给自足、对抗生长信号不敏感、逃避细胞凋亡、无限增殖潜能、持续血管生成、组织侵袭和转移,都是转化细胞的特征。鉴于核因子κB(NF-κB)能够控制许多参与这些过程的基因的表达和功能,它在肿瘤发生中是关键因素。实际上,NF-κB的组成型激活是许多人类肿瘤的共同特征,而其在炎症期间的持续激活使正常细胞易于发生肿瘤转化。由于已证明抑制NF-κB可抑制转化细胞的致癌潜能,因此靶向NF-κB在癌症的预防和治疗中应是有效的。

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