Recombinant immunotoxins development for HER2-based targeted cancer therapies
Recombinant immunotoxins development for HER2-based targeted cancer therapies
نویسندگان: رضا محمودی , حسن دیانت مقدم , سمانه سیاپوش , وحدت پورطهماسبی , محمد رحمتی , رضا صلاحلو
کلمات کلیدی: Monoclonal antibody, Recombinant immunotoxin, Cytolytic fusion protein, Immunoapoptin,
ImmunoRNase
نشریه: 6054 , 470 , 21 , 2021
| نویسنده ثبت کننده مقاله |
محمد رحمتی |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
دانشکده علوم نوین پزشکی |
| کد مقاله |
76748 |
| عنوان فارسی مقاله |
Recombinant immunotoxins development for HER2-based targeted cancer therapies |
| عنوان لاتین مقاله |
Recombinant immunotoxins development for HER2-based targeted cancer therapies |
| ناشر |
7 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
خیر |
| عنوان نشریه (خارج از لیست فوق) |
|
| نوع مقاله |
Review Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| Understanding the molecular mechanisms of cancer biology introduces targeted therapy as a complementary
method along with other conventional therapies. Recombinant immunotoxins are tumor specific antibodies that
their recognizing fragment is utilized for delivering modified toxins into tumor cells. These molecules have been con‑
sidered as a targeted strategy in the treatment of human cancers. HER2 tumor biomarker is a transmembrane tyrosine
kinase receptor that can be used for targeted therapies in the forms of anti‑HER2 monoclonal antibodies, antibody–
drug conjugates and immunotoxins. There have been many studies on HER2‑based immunotoxins in recent years,
however, little progress has been made in the clinical field which demanded more improvements. Here, we summa‑
rized the HER2 signaling and it’s targeting using immunotherapeutic agents in human cancers. Then, we specifically
reviewed anti‑HER2 immunotoxins, and their strengths and drawbacks to highlight their promising clinical impact |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Paper 1.pdf | 1400/06/16 | 1452724 | دانلود |