Modulation of molecular mechanisms involved in protein synthesis machinery as a new tool for the control of cell proliferation

被引:71
作者
Caraglia, M
Budillon, A
Vitale, G
Lupoli, G
Tagliaferri, P
Abbruzzese, A
机构
[1] Univ Naples 2, Dipartimento Biochim & Biofis, I-80138 Naples, Italy
[2] Ist Nazl Tumori, Naples, Italy
[3] Univ Naples Federico II, Dipartimento Endocrinol & Oncol Mol & Clin, Naples, Italy
[4] Magna Graecia Univ Catanzaro, Dipartimento Med Sperimentale, Catanzaro, Italy
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2000年 / 267卷 / 13期
关键词
signal transduction; therapy; translation; tumour;
D O I
10.1046/j.1432-1327.2000.01465.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In the past years, the attention of scientists has focused mainly on the study of the genetic information and alterations that regulate eukaryotic cell proliferation and that lead to neoplastic transformation. All therapeutic strategies against cancer are, to date, directed at DNA either with cytotoxic drugs or gene therapy. Little or no interest has been aroused by protein synthesis mechanisms. However, an increasing body of data is emerging about the involvement of translational processes and factors in control of cell proliferation, indicating that protein synthesis can be an additional target for anticancer strategies. In this paper we review the novel insights on the biochemical and molecular events leading to protein biosynthesis and we describe their involvement in cell proliferation and tumorigenesis. A possible mechanistic explanation is given by the interactions that occur between protein synthesis machinery and the proliferative signal transduction pathways and that are therefore suitable targets for indirect modulation of protein synthesis. We briefly describe the molecular tools used to block protein synthesis and the attempts made at increasing their efficacy. Finally, we propose a new multimodal strategy against cancer based on the simultaneous intervention on protein synthesis and signal transduction.
引用
收藏
页码:3919 / 3936
页数:18
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