The clofarabine effects on apoptosis induction and p53rR2 gene expression in breast cancer cell line (T47D)

The clofarabine effects on apoptosis induction and p53rR2 gene expression in breast cancer cell line (T47D)


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نویسندگان: تیمور حضرتیان , محمد رحمتی

عنوان کنگره / همایش: 13 th Iranian International Congress of Toxicology 22-24- May 2015 , Iran (Islamic Republic) , Urmia , 2015

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نویسنده ثبت کننده مقاله تیمور حضرتیان
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 70132
عنوان فارسی مقاله The clofarabine effects on apoptosis induction and p53rR2 gene expression in breast cancer cell line (T47D)
عنوان لاتین مقاله The clofarabine effects on apoptosis induction and p53rR2 gene expression in breast cancer cell line (T47D)
نوع ارائه سخنرانی
عنوان کنگره / همایش 13 th Iranian International Congress of Toxicology 22-24- May 2015
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش Iran (Islamic Republic)
شهر محل برگزاری کنگره/ همایش Urmia
سال انتشار/ ارائه شمسی 1394
سال انتشار/ارائه میلادی 2015
تاریخ شمسی شروع و خاتمه کنگره/همایش 1394/03/01 الی 1394/03/03
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Department of Parasitology, faculty of medicine, Tabriz university of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
تیمور حضرتیانچهارم
محمد رحمتیدوم

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عنوان متن
کلمات کلیدیapoptosis, breast cancer, DNA damage, gene expression
خلاصه مقالهIntroduction: clofarabine is a purine nucleoside analogue and inhibitor of ribonucleotide reductase enzyme complex (RR) that is used in treatment of blood cancers. Clofarabine-3P binds to RR and inhibits the conversion of NTPs to dNTPs. Low level of dNTP disrupts repairing and replication of DNA that results in induction of p53 and p53R2 subsequently. Purpose: in this study we investigate the effect of clofarabine in induction of apoptosis in P53R2 expression and apoptosis in T47D breast cancer cell line. Materials & Methods: T47D cell line was treated with different clofarabine concentration in three time: 24, 48 and 72h. Then by MTTassay the IC50 of clofarabine was determined. After treating cells, total RNA of them was extracted and their cDNA was built by Reverse Transcriptase enzyme. Then Real Time PCR was done. The Annexine V and PI was used to detection of apoptosis by flow-cytometry method. Result: IC50 for 48 and 72h was determined as 3 and 2.5μM respectively and the 24h treatment hasn’t cytotoxicicity on these cells. Clofarabine induces P53R2 expression in different time treatment of 48 and 72h. In 48h treatment P53R2 gene expression was 1.24 fold compared with control sample (1 fold), for 72h gene expression was 1.77 fold. Also the result of flowcytometry has shown 13.45 and 37.2 percent apoptosis induction for 48 and 72h treatment Conclusion: With regard to the above finding, clofarabine can induces apoptosis through induction of P53R2 in T47D cell line, so it can be considered for more investigation as drug in breast cancer (epithelial cancer cells) treatment.

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Abstract Clofarabine.pdf1398/09/10215408دانلود
Certificate Clofarabine.jpg1398/09/10355589دانلود