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以 p70 S6 激酶为靶点治疗卵巢癌。

Exploiting p70 S6 kinase as a target for ovarian cancer.

机构信息

University of Hong Kong, School of Biological Sciences, 4S-14 Kadoorie Biological Sciences Building, Pokfulam Road, Hong Kong, China.

出版信息

Expert Opin Ther Targets. 2012 Jun;16(6):619-30. doi: 10.1517/14728222.2012.684680. Epub 2012 May 7.

Abstract

INTRODUCTION

The p70 S6 kinase (p70(S6K)) is frequently active in ovarian and a wide range of cancer types, and it has a crucial role in several processes considered hallmarks of cancer. Therefore, blocking p70(S6K) expression or activity may present a promising strategy for anticancer treatment.

AREAS COVERED

The current understanding of the molecular mechanisms that govern p70(S6K) regulation as well as its tumorigenic effects, which are involved in the initiation and progression in ovarian cancer, in particular the emerging new role of p70(S6K) in cell migration, which is a prerequisite of tumor metastasis. The p70(S6K) cellular substrates and/or interacting proteins. The current state of drugs that target this kinase, either alone or in combination with other targeted agents.

EXPERT OPINION

Targeting p70(S6K) through the use of small-molecule inhibitors, microRNAs and natural compounds may represent a beneficial new avenue for cancer therapy and opens new areas of investigation in p70(S6K) biology.

摘要

简介

p70 S6 激酶(p70(S6K))在卵巢癌和多种癌症类型中经常活跃,并且在被认为是癌症特征的几个过程中起着关键作用。因此,阻断 p70(S6K)的表达或活性可能是一种有前途的抗癌治疗策略。

涵盖领域

目前对控制 p70(S6K)调节及其致癌作用的分子机制的理解,这些作用涉及卵巢癌的发生和进展,特别是 p70(S6K)在细胞迁移中的新出现的作用,这是肿瘤转移的先决条件。p70(S6K)的细胞底物和/或相互作用蛋白。目前针对这种激酶的药物的状态,无论是单独使用还是与其他靶向药物联合使用。

专家意见

通过使用小分子抑制剂、microRNAs 和天然化合物靶向 p70(S6K),可能代表着癌症治疗的一个有益的新途径,并为 p70(S6K)生物学开辟了新的研究领域。

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