Induction of mTOR signaling pathway in the progression of papillary thyroid cancer

Induction of mTOR signaling pathway in the progression of papillary thyroid cancer


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نویسندگان: الهام امجد سقین سرا , سولماز اثناعشری , بابک سکوتی

کلمات کلیدی: mTOR signaling pathway PTC Papillary thyroid cancer Gene Biomarker

نشریه: 36918 , 100704 , 24 , 2020

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نویسنده ثبت کننده مقاله بابک سکوتی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات بیوتکنولوژی(زیست فناوری)
کد مقاله 71629
عنوان فارسی مقاله Induction of mTOR signaling pathway in the progression of papillary thyroid cancer
عنوان لاتین مقاله Induction of mTOR signaling pathway in the progression of papillary thyroid cancer
ناشر 3
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
عنوان نشریه (خارج از لیست فوق)
نوع مقاله متاآنالیز
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Papillary thyroid carcinoma (PTC) is the most frequent (more than 85%) malignancy among the four pathological types of thyroid cancer. Since enhancements of survival and recurrence rates of the disease as well as early diagnosis are essential, the genome-wide investigation for identifying robust biomarkers for PTC patients is necessary. In the current research, two independent gene expression omnibus (GEO) datasets resulted from systematically searching the NCBI-GEO database and applying the inclusion and exclusion criteria for PTC patients. Then, the identifcation of signifcant biomarkers through a meta-analysis approach used the associated genes of the mTOR signaling pathway. The survival analysis of the determined genes included overall survival (OS) and recurrence-free survival (RFS) rates based on The Cancer Genome Atlas dataset. Furthermore, the analysis and virtual screening process were carried out for fnding potential drugs and drug-like ligands. The analysis outcomes reveal three statistically signifcant downregulated biomarkers IRS1, DEPTOR, and PRKCA between PTC and healthy tissues with experimental literature confrmation. Moreover, the survival analysis shows that DEPTOR and PRKCA have vital roles in RFS (p-value = .012) and OS (p-value = .045) rates, respectively. However, IRS1 does not present signifcant p-value in terms of RFS and OS rates. The GDIdbi webserver found twenty, three, and four potential drugs for PRKCA, DEPTOR, and IRS1. And two molecules had structural interactions with IRS1 with four hydrogen bond acceptors through the virtual screening procedure. Consequently, the critical role of genome-wide association studies (GWAS) should not be of ignorance in diagnosing PTC patients. Furthermore, the outcomes of such GWAS investigations need to be carefully involved in the future development of new therapeutic agents.

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نویسنده نفر چندم مقاله
الهام امجد سقین سرااول
سولماز اثناعشریاول
بابک سکوتیسوم

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1-s2.0-S2214540020300591-main.pdf1399/01/222434122دانلود