Statins and Alkylphospholipids as New Anticancer Agents Targeting Lipid Metabolism

被引:15
作者
Apostolova, Sonia N. [1 ]
Toshkova, Reneta A. [2 ]
Momchilova, Albena B. [1 ]
Tzoneva, Rumiana D. [1 ]
机构
[1] Bulgarian Acad Sci, Inst Biophys & Biomed Engn, Acad G Bonchev Str,Bl 21, Sofia 1113, Bulgaria
[2] Bulgarian Acad Sci, Inst Expt Morphol Pathol & Anthropol Museum, Acad G Bonchev Str,Bl 25, Sofia 1113, Bulgaria
关键词
Statins; alkylphospholipids; lipid metabolism; intracellular signaling; antitumor potential; SIMVASTATIN INDUCES APOPTOSIS; HEPATOCELLULAR-CARCINOMA CELLS; COA REDUCTASE INHIBITORS; BREAST-CANCER CELLS; IN-VIVO; CYCLE ARREST; CHOLESTEROL; DEATH; AKT; PERIFOSINE;
D O I
10.2174/1871520616666160624093955
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The partial efficacy and high toxicity of the current anticancer chemotherapeutics as well as the development of multiple drug resistance are the major problems in cancer therapy. Therefore, there is an emergency need for the development of novel well-tolerated anticancer agents with different mode of action that could be successfully used in combination with other drugs as an adjuvant therapy. The inhibition of intracellular signaling pathways associated with cancer growth and invasiveness is a main therapeutic approach in cancer treatment. It is well known that lipid metabolism is involved in the regulation of key cellular processes such as proliferation, differentiation and apoptosis. Statins and alkylphospholipids are both relatively new synthetic agents with considerable anticancer properties that disturb lipid metabolism and subsequently modulate proliferation and cell survival signaling pathways, leading to apoptosis. Numerous in vitro and in vivo studies have shown promising results for the use of statins and alkylphospholipids as potential therapeutic agents in the treatment of various human malignancies. However, more investigations and clinical trials are needed to assess their optimal safe dose and maximal efficacy and better understand the molecular mechanisms underlying the antitumor effects of these drugs.
引用
收藏
页码:1512 / 1522
页数:11
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