کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5907086 1159997 2013 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Short CommunicationInsulin-like factor binding protein-3 promotes the G1 cell cycle arrest in several cancer cell lines
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
پیش نمایش صفحه اول مقاله
Short CommunicationInsulin-like factor binding protein-3 promotes the G1 cell cycle arrest in several cancer cell lines
چکیده انگلیسی

Insulin-like growth factor binding protein-3 (IGFBP-3) is a multi-functional protein known to induce apoptosis of various cancer cells in an insulin-like growth factor (IGF)-dependent and IGF-independent manner. In our previous study, we found that IGFBP-3 induced apoptosis through the activation of caspases in 786-O cells. In this study, we further examined that whether IGFBP-3 induced apoptosis through the induction of cell cycle arrest in 786-O, A549 and MCF-7 cells. Our results showed that overexpressed IGFBP-3 resulted in typical apoptotic ultrastructures in A549 cells under transmission electron microscope. The result of flow cytometry analysis indicated that IGFBP-3 arrested the cell cycle at G1-S phase in 786-O, A549 and MCF-7 cells. In A549 cells, quantitative real-time PCR and Western blot analysis showed a significant change in the expression of cell cycle-regulated proteins-a decrease in cyclin E1 expression, an increase in p21 expression. These results indicate a possible mechanism for G1 cell cycle arrest by IGFBP-3. Taken together, cyclin E1 and p21 may play important roles in the IGFBP-3-inducing G1 cell cycle arrest and apoptosis in several human cancer cells.

► IGFBP-3 resulted in typical apoptotic ultrastructures in A549 cells. ► IGFBP-3 could induce apoptosis in MCF-7 cells, especially the early apoptosis. ► IGFBP-3 arrested the cell cycle at G1-S phase in 786-O, A549 and MCF-7 cells. ► IGFBP-3 decreased the cyclinE1 expression and increased the p21 expression.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 512, Issue 1, 1 January 2013, Pages 127-133
نویسندگان
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