کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1930077 1050489 2012 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Frizzled-8 as a putative therapeutic target in human lung cancer
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Frizzled-8 as a putative therapeutic target in human lung cancer
چکیده انگلیسی

Lung cancer is the leading cause of cancer related deaths worldwide. It is necessary to better understand the molecular mechanisms involved in lung cancer in order to develop more effective therapeutics for the treatment of this disease. Recent reports have shown that Wnt signaling pathway is important in a number of cancer types including lung cancer. However, the role of Frizzled-8 (Fzd-8), one of the Frizzled family of receptors for the Wnt ligands, in lung cancer still remains to be elucidated. Here in this study we showed that Fzd-8 was over-expressed in human lung cancer tissue samples and cell lines. To investigate the functional importance of the Fzd-8 over-expression in lung cancer, we used shRNA to knock down Fzd-8 mRNA in lung cancer cells expressing the gene. We observed that Fzd-8 shRNA inhibited cell proliferation along with decreased activity of Wnt pathway in vitro, and also significantly suppressed A549 xenograft model in vivo (p < 0.05). Furthermore, we found that knocking down Fzd-8 by shRNA sensitized the lung cancer cells to chemotherapy Taxotere. These data suggest that Fzd-8 is a putative therapeutic target for human lung cancer and over-expression of Fzd-8 may be important for aberrant Wnt activation in lung cancer.


► Fzd-8 is over-expressed in human lung cancer.
► shRNA knock-down of Fzd-8 inhibits proliferation and Wnt pathway in lung cancer cells.
► shRNA knock-down of Fzd-8 suppresses tumor growth in vivo.
► shRNA knock-down Fzd-8 sensitizes lung cancer cells to chemotherapy Taxotere.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 417, Issue 1, 6 January 2012, Pages 62–66
نویسندگان
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