کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1928636 | 1050400 | 2013 | 5 صفحه PDF | دانلود رایگان |

• ADEP1 and 2 potently inhibited the growth of three renal carcinoma cells.
• ADEP1 and 2 inhibited renal carcinoma cell growth by G1 cell cycle arrest.
• ADEP1 decreased the activity of MAPK–ERK and expression of cyclin D1 protein.
• ADEP1 is a promising candidate for developing antitumor agent.
Acyldepsipeptides are a group of potent antibiotics discovered in the secondary metabolites of Streptomyces species. However, besides the function of antibiotics, no other activities have been reported about these important compounds so far. In the course of searching the natural products as chemotherapeutic agents for renal cell carcinoma, we found that ADEP1, a major metabolic component of Streptomyces hawaiiensis NRRL 15010, could effectively inhibit the growth of 786-O, 769-P, and ACHN renal carcinoma cells in MTT assay. Flow cytometric analysis demonstrated that ADEP1 could block the cell cycle arrested at G1 phase. Moreover, it was found that ADEP1 down-regulated the expressions of cyclin D1, CDK4 and PCNA and inhibited activity of MAPK–ERK pathway by detection of decreased expression of phosphorylated ERK1/2 and c-Fos in 786-O and 769-P cells by Western blotting. To our knowledge, this is the first report concerning to the antitumor activities of acyldepsipeptides. Based on these results, ADEP1 may become a promising lead compound to be developed a novel chemotherapeutic agent for treatment of renal carcinoma.
Journal: Biochemical and Biophysical Research Communications - Volume 438, Issue 3, 30 August 2013, Pages 468–472