Ishii T, Hayashi K, Hida T, Yamamoto Y, Nozaki Y
Pharmaceutical Discovery Research Division, Takeda Chemical Industries, Ltd., Tsukuba, Ibaraki, Japan.
J Antibiot (Tokyo). 2000 Aug;53(8):765-78. doi: 10.7164/antibiotics.53.765.
A novel Ras-farnesyltransferase inhibitor designated TAN-1813 was isolated from the culture broth of a fungus strain, FL-41510, isolated as a plant endophyte. The producer was taxonomically characterized as Phoma sp. FL-41510. TAN-1813 inhibited rat brain farnesyltransferase and geranylgeranyltransferase I activity with IC50 values of 23 microg/ml and 47/microg/ml, respectively. TAN-1813 showed mixed-type inhibition with respect to farnesylpyrophosphate and noncompetitive inhibition with respect to a K-Ras C-terminal peptide. It also inhibited the in situ farnesylation of cellular Ras proteins in a K-ras transformant (NIH3T3/K-ras) of mouse embryonic fibroblast cell line NIH3T3. TAN- 1813 inhibited the proliferation of various human cancer cells, some of which harbor activated ras alleles, with IC50 values of 15 approximately 110 ng/ml as well as that of NIH3T3 and NIH3T3/K-ras cells with IC50S of 540 and 310 ng/ml, respectively. Flow cytometric analysis indicated that TAN-1813 arrests NIH3T3/K-ras cells at both G1 and G2/M phases of the cell cycle. In addition, TAN-1813 was found to induce morphological reversion of NIH3T3/K-ras cells from the transformed phenotype. Antitumor activity of TAN-1813 against human fibrosarcoma HT-1080 and NIH3T3/K-ras tumors in nude mice was also verified.
从一株作为植物内生菌分离得到的真菌菌株FL-41510的培养液中,分离出一种名为TAN-1813的新型Ras-法尼基转移酶抑制剂。该产生菌在分类学上被鉴定为茎点霉属Phoma sp. FL-41510。TAN-1813抑制大鼠脑法尼基转移酶和香叶基香叶基转移酶I的活性,其IC50值分别为23微克/毫升和47微克/毫升。TAN-1813对法尼基焦磷酸表现出混合型抑制,对K-Ras C末端肽表现出非竞争性抑制。它还抑制小鼠胚胎成纤维细胞系NIH3T3的K-ras转化子(NIH3T3/K-ras)中细胞Ras蛋白的原位法尼基化。TAN-1813抑制多种人类癌细胞的增殖,其中一些含有激活的ras等位基因,IC50值为15至110纳克/毫升,对NIH3T3和NIH3T3/K-ras细胞的IC50值分别为540和310纳克/毫升。流式细胞术分析表明,TAN-1813使NIH3T3/K-ras细胞停滞在细胞周期的G1期和G2/M期。此外,发现TAN-1813可诱导NIH3T3/K-ras细胞从转化表型发生形态逆转。还验证了TAN-1813对裸鼠体内人纤维肉瘤HT-1080和NIH3T3/K-ras肿瘤的抗肿瘤活性。