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靶向天然萜类化合物的凋亡途径:在乳腺癌和前列腺癌治疗中的意义。

Targeting apoptosis pathway with natural terpenoids: implications for treatment of breast and prostate cancer.

机构信息

The Prevention Program, Barbara Ann Karmanos Cancer Institute, and Department of Oncology, School of Medicine, Wayne State University, Detroit, Michigan 48201, USA.

出版信息

Curr Drug Targets. 2010 Jun;11(6):733-44. doi: 10.2174/138945010791170842.

Abstract

Terpenoids represent a large and diverse class of naturally occurring compounds found in a variety of fruits, vegetables and medicinal plants. Structurally some of the terpenoids are similar to human hormones. A diet rich in terpenoids is inversely related with the risk of chronic diseases including cancers. Breast and prostate cancers are hormone-related diseases and the second leading cause of female and male cancer mortality. Diterpenoid paclitaxel, and its semi-synthetic analogue docetaxel, have entered clinical use against established breast and prostate cancers. Here we reviewed potential molecular targets and biological properties of natural terpenoids, including monoterpenoids, diterpenoids, triterpenoids and tetraterpenoids, and their applications in treatment of human breast and prostate cancers. These terpenoids are able to inhibit tumor cell proliferation and induce tumor cell death by inhibiting multiple cancer-specific targets including the proteasome, NF-kappaB, and antiapoptotic protein Bcl-2. The efficacy of these terpenoids against breast or prostate cancer cells, as demonstrated in pre-clinical studies support clinical application of these naturally occurring terpenoids in treatment of hormone-related human cancers.

摘要

萜类化合物是一大类结构多样的天然化合物,存在于各种水果、蔬菜和药用植物中。一些萜类化合物在结构上与人体激素相似。富含萜类化合物的饮食与包括癌症在内的慢性疾病的风险呈负相关。乳腺癌和前列腺癌是与激素相关的疾病,也是女性和男性癌症死亡的第二大主要原因。二萜紫杉醇及其半合成类似物多西紫杉醇已被用于治疗已确诊的乳腺癌和前列腺癌。在这里,我们回顾了天然萜类化合物(包括单萜类、二萜类、三萜类和四萜类)的潜在分子靶点和生物学特性,及其在治疗人类乳腺癌和前列腺癌中的应用。这些萜类化合物能够通过抑制多种癌症特异性靶点,包括蛋白酶体、NF-κB 和抗凋亡蛋白 Bcl-2,抑制肿瘤细胞增殖并诱导肿瘤细胞死亡。这些萜类化合物在临床前研究中对乳腺癌或前列腺癌细胞的疗效支持将这些天然存在的萜类化合物应用于治疗与激素相关的人类癌症。

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