Volume 26, Issue 9 (12-2019)
RJMS 2019, 26(9): 29-38 |
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Moshfegh P, Aletaha M, Baradaran B. The effect of miR-34a replacement in the proliferation inhibition of cancerous cell line of esophagus. RJMS 2019; 26 (9) :29-38
URL: http://rjms.iums.ac.ir/article-1-5535-en.html
URL: http://rjms.iums.ac.ir/article-1-5535-en.html
Tabriz University of Medical Sciences, Tabriz, Iran , manal239@yahoo.com
Abstract: (3193 Views)
Background: Because of its malignancy and poor prognosis, esophageal cancer is the sixth cause of death around the world. MiR-34a is a tumor suppressor. The miRNA-34 family is involved in suppressing the tumor and oncogenic pathways in some cancers. The purpose of this research is to determine the changes in the expression of the Vimentin gene after the replacement of miR-34a, on the other hand the effect of replacing this micro-RNA on cell proliferation is determined.
Methods: After cultivating the TE-8 cell line, miR-34a was replaced in esophageal cancer cells and after miR-34a replacement, Vimentin gene expression was evaluated using qRT-PCR method. Cell proliferation in the TE-8 cell line was evaluated in effective time and dose after the replacement of mir-34a by the MTT method.
Results: Replacing miR-34a in the TE-8 cell line significantly reduced the expression of Vimentin (p<0.0001). Mir-34a could (at an effective dose) within 24 hours significantly reduce cell proliferation (p<0.0001).
Conclusion: Possibly, the replacement of miR-34a could have a therapeutic role in esophageal cancer.
Methods: After cultivating the TE-8 cell line, miR-34a was replaced in esophageal cancer cells and after miR-34a replacement, Vimentin gene expression was evaluated using qRT-PCR method. Cell proliferation in the TE-8 cell line was evaluated in effective time and dose after the replacement of mir-34a by the MTT method.
Results: Replacing miR-34a in the TE-8 cell line significantly reduced the expression of Vimentin (p<0.0001). Mir-34a could (at an effective dose) within 24 hours significantly reduce cell proliferation (p<0.0001).
Conclusion: Possibly, the replacement of miR-34a could have a therapeutic role in esophageal cancer.
Type of Study: Research |
Subject:
Hematology & oncology
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