این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
صفحه اصلی
درباره پایگاه
فهرست سامانه ها
الزامات سامانه ها
فهرست سازمانی
تماس با ما
JCR 2016
جستجوی مقالات
چهارشنبه 26 آذر 1404
Cell Journal
، جلد ۲۶، شماره ۱، صفحات ۵۱-۶۱
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Candidate Biomarkers for Targeting in Type 1 Diabetes; A Bioinformatic Analysis of Pancreatic Cell Surface Antigens
چکیده انگلیسی مقاله
Objective: Type 1 diabetes (T1Ds) is an autoimmune disease in which the immune system invades and destroys
insulin-producing cells. Nevertheless, at the time of diagnosis, about 30-40% of pancreatic beta cells are healthy and
capable of producing insulin. Bi-specific antibodies, chimeric antigen receptor regulatory T cells (CAR-Treg cells), and
labeled antibodies could be a new emerging option for the treatment or diagnosis of type I diabetic patients. The aim
of the study is to choose appropriate cell surface antigens in the pancreas tissue for generating an antibody for type I
diabetic patients.
Materials and Methods: In this bioinformatics study, we extracted pancreas-specific proteins from two large
databases; the Human Protein Atlas (HPA) and Genotype-Tissue Expression (GTEx) Portal. Pancreatic-enriched
genes were chosen and narrowed down by Protter software for the investigation of accessible extracellular domains.
The immunohistochemistry (IHC) data of the protein atlas database were used to evaluate the protein expression of
selected antigens. We explored the function of candidate antigens by using the GeneCards database to evaluate the
potential dysfunction or activation/hyperactivation of antigens after antibody binding.
Results: The results showed 429 genes are highly expressed in the pancreas tissue. Also, eighteen genes encoded
plasma membrane proteins that have high expression in the microarray (GEO) dataset. Our results introduced four
structural proteins, including NPHS1, KIRREL2, GP2, and CUZD1, among all seventeen candidate proteins.
Conclusion: The presented antigens can potentially be used to produce specific pancreatic antibodies that guide CARTreg,
bi-specific, or labeling molecules to the pancreas for treatment, detection, or other molecular targeted therapy
scopes for type I diabetes.
کلیدواژههای انگلیسی مقاله
Bioinformatics, Cell Surface Antigens, Molecular Targeted Therapies, Pancreatic islets, Type 1 Diabetes
نویسندگان مقاله
Hamed Dabiri |
Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran
Mahdi Habibi-Anbouhi |
National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran
Vahab Ziaei |
National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran
Zahra Moghadasi |
National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran
Majid Sadeghizadeh |
Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran
Ensiyeh Hajizadeh-Saffar |
Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
نشانی اینترنتی
https://www.celljournal.org/article_708536_70a8e695bc5643def0ab5939b75b94bf.pdf
فایل مقاله
فایلی برای مقاله ذخیره نشده است
کد مقاله (doi)
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده
برگشت به:
صفحه اول پایگاه
|
نسخه مرتبط
|
نشریه مرتبط
|
فهرست نشریات