*Five Years Citation in Google scholar (2016 - 2020) is. 1451*   *    IJPR IS INDEXED IN ELSEVIER EMBASE & EBSCO *       

logo

INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH

A Step Towards Excellence
Published by : Advanced Scientific Research
ISSN
0975-2366
Current Issue
Article In Press
No Data found.
ADOBE READER

(Require Adobe Acrobat Reader to open, If you don't have Adobe Acrobat Reader)

Index Page 1
Click here to Download
IJPR 9[3] July - September 2017 Special Issue

July - September 9[3] 2017

Click to download
 

Article Detail

Label
Label
Effect of SIRT1 Activators on Human Follicular Thyroid Cancer

Author: LAMEES TALIB, MUSTAFA GHAZI AL-ABBASSI, BASMA TALIB AL-SUDANI
Abstract: Sirtuins are NAD+ dependent deacetylase enzymes, SIRT1 is the most studied type of human sirtuins. SIRT1 plays a dual role in cancer where it can be a tumor promoter or tumor suppressor. The activation of SIRT1 by aptamer shows a tumor-suppressive effect in multiple cancer cell lines. This study aims to study the effect of activation of SIRT1 by aptamer on FTC236 and FTC238 by studying the mechanism of p53 and MAPK. The methodology includes circularization of aptamer, cell line culture, MTT assay and determination of IC50, cell fractionation, immunoblotting, transfection of p53 antisense oligonucleotides, and determination of c-fos, p21, and GAPDH mRNA. The result shows that the activation of SIRT1 by aptamer could inhibit significantly the growth of FTC236 and FTC238 cell lines, this inhibition occurs through the activation of MAPK (ERK1/ERK2) and subsequent expression of p21 and c-fos.
Keyword: MAPK (ERK1/ERK2), p21, c-fos, MTT assay.
DOI: https://doi.org/10.31838/ijpr/2020.12.04.230
Download: Request For Article
 




ONLINE SUBMISSION
USER LOGIN
Username
Password
Login | Register
News & Events
SCImago Journal & Country Rank

Terms and Conditions
Disclaimer
Refund Policy
Instrucations for Subscribers
Privacy Policy

Copyrights Form

0.12
2018CiteScore
 
8th percentile
Powered by  Scopus
Google Scholar

hit counters free