دوره 10، شماره 1 - ( 10-1399 )                   | برگشت به فهرست نسخه ها

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Mohammadi C, Mahdavinezhad A, Saidijam M, Bahreini F, Sedighi Pashaki A, Gholami M H et al . DCLK1 Inhibition Sensitizes Colorectal Cancer Cells to Radiation Treatment. Int J Mol Cell Med 2021; 10 (1) :23-33
URL: http://ijmcmed.org/article-1-1531-fa.html
DCLK1 Inhibition Sensitizes Colorectal Cancer Cells to Radiation Treatment. مجله بین المللی سلولی و مولکولی. 1399; 10 (1) :23-33

URL: http://ijmcmed.org/article-1-1531-fa.html

DCLK1 Inhibition Sensitizes Colorectal Cancer Cells to Radiation Treatment
:   (5347 مشاهده)
Colorectal cancer (CRC) is one of the most prevalent diagnosed cancers and a common cause of cancer-related mortality. Despite effective clinical responses, a large proportion of patients undergo resistance to radiation therapy. Therefore, the identification of efficient targeted therapy strategies would be beneficial to overcome cancer radioresistance. Doublecortin-like kinase 1 (DCLK1) is an intestinal and pancreatic stem cell marker that showed overexpression in a variety of cancers. The transfection of DCLK1 siRNA to ‎normal HCT-116 cells was performed, and then cells were irradiated with X-rays. The effects of DCLK1 inhibition on cell survival, apoptosis, cell cycle, DNA damage response (ATM and γH2AX proteins), epithelial- mesenchymal transition (EMT) related genes (vimentin, N‐cadherin, and E-cadherin), cancer stem cells markers (CD44, CD133, ALDH1, and BMI1), and β‐catenin signaling pathway (β‐catenin) were evaluated. DCLK1siRNA downregulated DCLK1 expression in HCT-116 cells at both mRNA and protein levels (P < 0.01). Colony formation assay showed a significantly reduced cell survival in the DCLK1 siRNA transfected group in comparison with the control group following exposure to 4 and 6 Gy doses of irradiation (P < 0.01). Moreover, the expression of cancer stem cells markers (P < 0.01), EMT related genes (P < 0.01), and DNA repair proteins including pATM (P < 0.01) and γH2AX (P < 0.001) were significantly decreased in the transfected cells in comparison with the nontransfected group after radiation. Finally, the cell apoptosis rate (P < 0.01) and the number of cells in the G0/G1 phase in the silencing DCLK1 group was increased (P < 0.01). These findings suggest that DCLK1 can be considered a promising therapeutic target for the treatment of radioresistant human CRC.
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نوع مطالعه: Original Article | موضوع مقاله: Cancer
دریافت: 1399/9/26 | پذیرش: 1399/12/9 | انتشار: 1399/11/2
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