Abstract

Background: Transcriptionally silencing is related to abnormal methylation of tumor suppressor gene promoters by the enzyme of DNA methylase (DNMT1) in an alternate way in prostate cancer development. Ghareghate (acciniumarctostaphylos) have polyphenols and anthocyanins which may be investigated as natural antioxidants in prostate cancer cells treating. Methods: In this study human invasive prostate cancer cell lines (PC3) were treated with various concentrations (156, 312, 625, 1250, 2500 µg/ml) of Ghareghate fruit extractions. DNMT1 expression levels and inhibition rates were assessed after 24, 48 hours by Q-RT-PCR and MTT test respectively. Results: DNMT1 expression rates in pc3 cell line which treated with Ghareghate extractions, reduced significantly comparing to control cells (p<0.001). Moreover it has demonstrated that Ghareghate extractions can significantly increase inhibition of cancer cells grow (p<0.001). The highest relative decrease of gene expression observed in 625µg/ml. Conclusion: Ghareghat extractions can be used as an antioxidant recourse for the purpose of cancer therapy and prevention.

Highlights

  • Silencing is related to abnormal methylation of tumor suppressor gene promoters by the enzyme of DNA methylase (DNMT1) in an alternate way in prostate cancer development

  • Ghareghat extractions can be used as an antioxidant recourse for the purpose of cancer therapy and prevention

  • ‫ٔيت‪ٛ‬ا٘ذ ث‪ّٛٙ ٝ‬اٖ آ٘تياوغيذاٖ‪ٞ‬بي ىجيْي در تيٕبر عزىبٖ پز‪ٚ‬عتبت ٔ‪ٛ‬رد ثزرعي لزار ٌيزد‪.‬‬ ‫روشکار‪ :‬عّ‪َٞٛ‬بي ت‪ٟ‬بخٕي رد‪ ٜ‬عزىب٘ي پز‪ٚ‬عتبت ا٘غب٘ي (‪ )PC3‬ثب غَّت‪ٞ‬بي ٔختّف اس ّقبر‪ٔ ٜ‬ي‪ ٜٛ‬لز‪ ٜ‬لبه (‪ٚ 625،1250 ،312 ،156‬‬ ‫‪ٔ 2500‬يىز‪ٌٚ‬زْ ثز ٔيّيِيتز) تيٕبر ٌزديذ‪ٔ .‬يشاٖ ثيبٖ صٖ ‪ DNMT1‬ثب ر‪ٚ‬ػ ‪ٔ ٚ Q-RT-PCR‬يشاٖ ٔ‪ٟ‬بر رؽذ عّ‪َٞٛ‬بي ‪ PC3‬ثب آسٔ‪ MTT ٖٛ‬در‬

Read more

Summary

Introduction

Silencing is related to abnormal methylation of tumor suppressor gene promoters by the enzyme of DNA methylase (DNMT1) in an alternate way in prostate cancer development.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call