دورية أكاديمية

The delivery of N-myc downstream-regulated gene 2 (NDRG2) self-amplifying mRNA via modified lipid nanoparticles as a potential treatment for drug-resistant and metastatic cancers

التفاصيل البيبلوغرافية
العنوان: The delivery of N-myc downstream-regulated gene 2 (NDRG2) self-amplifying mRNA via modified lipid nanoparticles as a potential treatment for drug-resistant and metastatic cancers
المؤلفون: Reznik Sandra E., Tiwari Amit K., Chavda Vivek, Ashby Jr Charles R.
المصدر: Medical Review, Vol 4, Iss 3, Pp 235-238 (2024)
بيانات النشر: De Gruyter, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
مصطلحات موضوعية: n-myc downstream-regulated gene 2 (ndrg2), cancer, self-amplifying mrna, nanoparticle, Medicine
الوصف: The protein, N-myc downstream-regulated gene 2 (NDRG2), a tumor suppressor, is significantly decreased or absent in many types of cancer. There is a significant negative correlation between the levels of NDRG2 and the development and progression of cancer tumor recurrence and tumor invasion, in different cancers. In contrast, the in vitro and in vivo overexpression of the NDRG2 protein decreases the proliferation, growth, adhesion and migration of many types of cancer cells. The in vitro overexpression of NDRG2 increases the efficacy of certain anticancer drugs in specific types of cancer cells. We hypothesize that the delivery of the mRNA of the NDRG2 protein, encapsulated by lipid nanoparticles, could represent a potential treatment of metastatic and drug-resistant cancers. This would be accomplished using a self-amplifying mRNA that encodes the NDRG2 protein and an RNA-dependent-RNA polymerase, obtained from an in vitrotranscribed (IVT) mRNA. The IVT mRNA would be encapsulated in a lipid nanoformulation. The efficacy of the nanoformulation would be determined in cultured cancer cells and if the results are positive, nude mice transplanted with either drug-resistant or metastatic drug-resistant cancer cells, would be treated with the nano- formulation and monitored for efficacy and adverse effects. If the appropriate preclinical studies indicate this formulation is efficacious and safe, it is possible it could be evaluated in clinical trials.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2749-9642
Relation: https://doaj.org/toc/2749-9642
DOI: 10.1515/mr-2024-0004
URL الوصول: https://doaj.org/article/ca6c365887044280b4d66ddfe8da6806
رقم الأكسشن: edsdoj.6c365887044280b4d66ddfe8da6806
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:27499642
DOI:10.1515/mr-2024-0004