Advancements of Adenovirus-Based Gene Therapy in Colorectal Cancer

Advancements of Adenovirus-Based Gene Therapy in Colorectal Cancer


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نویسندگان: الهام کمال کاظمی , ناصر هاشمی گورادل , فاطمه بادی پا , عفت علیزاده

عنوان کنگره / همایش: دومین کنگره بین المللی کنسر ژنتیکس (از ژن تا ژنومیکس) , Iran (Islamic Republic) , تهران , 2025

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نویسنده ثبت کننده مقاله عفت علیزاده
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده علوم نوین پزشکی
کد مقاله 88919
عنوان فارسی مقاله Advancements of Adenovirus-Based Gene Therapy in Colorectal Cancer
عنوان لاتین مقاله Advancements of Adenovirus-Based Gene Therapy in Colorectal Cancer
نوع ارائه پوسترو سخنرانی
عنوان کنگره / همایش دومین کنگره بین المللی کنسر ژنتیکس (از ژن تا ژنومیکس)
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش Iran (Islamic Republic)
شهر محل برگزاری کنگره/ همایش تهران
سال انتشار/ ارائه شمسی 1404
سال انتشار/ارائه میلادی 2025
تاریخ شمسی شروع و خاتمه کنگره/همایش 1404/08/01 الی 1404/08/03
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
الهام کمال کاظمیاول
ناصر هاشمی گورادلدوم
فاطمه بادی پاسوم
عفت علیزادهچهارم

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عنوان متن
کلمات کلیدیColorectal cancer, Gene therapy, Epigenetic, Adenovirus, Adenoviral vector, CRC patients
خلاصه مقالهIntroduction: Despite the recent advances in controlling Colorectal cancer (CRC), CRC remains the second leading cause of cancer deaths in the world. Like the other cancers, genetic and epigenetic alterations are involved in CRC progression and pathogenesis. Therefore, in comparison to conventional therapeutic approaches for the treatment of CRC, the recruitment of gene therapy methods seems to be a promising way for the treatment of patients with CRC. Gene therapy is mainly based on the process of gene transfer and gene-editing technologies to replace and correct defective genes. For successful gene therapy, in addition to identification of the target gene, the development of the appropriate delivery system is needed. Viral vectors are one of the most promising methods for gene therapy delivery to colorectal cancer patients. The genomics materials of these viruses can be engineered to successfully express the target genes in infected cells. In addition, viruses simultaneously lyse tumor cells and trigger both humoral and cellular immune responses in the tumor microenvironment. Among the several types of oncolytic viruses, Adenoviruses, a non-enveloped virus with linear double-stranded DNA, have emerged as promising candidates for a gene delivery vehicle and vaccine design due to their high transgene capacity, efficient gene transduction, genetic stability, production at high titer, and ability to infect both dividing and non-dividing cells. In this paper, we will review the results of preclinical and clinical studies to elucidate the efficacy and safety of adenovirus-based gene therapy methods in colorectal cancer patients. Methods: We searched PubMed, Google Scholar, and clinicaltrials.gov databases based on appropriate keywords of colorectal cancer, gene therapy, epigenetic, adenovirus, adenoviral vector, CRC patients to identify original articles involving adenoviruses in colorectal cancer gene therapy. Result: Several studies preclinically and clinically investigated the therapeutic role of adenoviruses in CRC treatment. For example, Oday Hamid demonstrated the antitumor activity, safety, immune response, and replication of CI-1042 (ONYX-015), an E1B 55-kd gene-deleted replication-selective adenovirus in the CRC patients, proving the efficacy of CI-1042 intravenously to patients with metastatic colorectal cancer. In addition, the tumor-specific apoptotic activity of adenovirus encoding the p53 transgene in colorectal cancer patients was in the phase 1 study of IA. Atencio et al, in 2006. Intratumorally treatment of athymic mice with colon cancer with AdCDUPRT (adenoviral vector encoding the uracil phosphoribosyltransferase) significantly reduced tumor growth rates compared with untreated controls. Adenoviral-mediated transfer of PTEN (Ad-PTEN) suppressed cell divisions and induced apoptosis in CRC. Conclusion: Preclinical and clinical studies have demonstrated the safety and preliminary efficacy of adenoviruses in targeting and successful gene therapy of CRC. Hence, Adenovirus mediated gene therapy could be translated to clinic in the future.

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