Khosravanian, Mohammad Javad and Mirzaei, Yousef and Mer, Ali Hussein and Keyhani-Khankahdani, Maryam and Abdinia, Fatemeh Sarina and Misamogooe, Fatemeh and Amirkhani, Zahra and Bagheri, Nader and Meyfour, Anna and Jahandideh, Saeed and Barpour, Nesa and Nikmanesh, Yousef and Shahsavarani, Hosein and Abdollahpour-Alitappeh, Meghdad (2024) Nectin-4-directed Antibody-drug Conjugates (ADCs): Spotlight on Preclinical and Clinical Evidence. Life Sciences, 352. p. 122910. ISSN 00243205
Article_LS_11-07-2024.pdf - Published Version
Available under License Creative Commons Attribution Non-commercial No Derivatives.
Download (385kB)
Abstract
Nectin-4 (Nectin cell adhesion molecule 4), a type I transmembrane cell adhesion protein, was demonstrated to be overexpressed in a variety of tumors, making it an attractive antigen for targeted therapies such as antibody-drug conjugates (ADCs). Of great note, the US Food and Drug Administration (FDA)-approval of the first Nectin-4-directed ADC, enfortumab vedotin (EV), in urothelial cancer (UC) not only introduced Nectin-4 as a clinically validated and reliable target antigen but also confirmed the evolving role of Nectin-4-directed ADCs as novel and promising cancer therapeutics. In addition to EV, there have been or are currently being seven and eleven Nectin-4-directed ADCs, respectively, in various stages of clinical trials and preclinical development, offering a promising future for the treatment of Nectin-4-positive cancer patients. This study reviewed clinical- and preclinical-stage Nectin-4-directed ADCs.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Nectin-4 , Antibody-drug Conjugates (ADCs) , Enfortumab Vedotin (EV) , Urothelial Cancer (UC) , Targeted Cancer Therapy |
| Subjects: | Q Science > Q Science (General) Q Science > QD Chemistry |
| Divisions: | Department of Medical Biochemical Analysis > Research papers |
| Depositing User: | ePrints Depositor |
| Date Deposited: | 20 Nov 2024 14:09 |
| Last Modified: | 20 Nov 2024 14:09 |
| URI: | https://eprints.cihanuniversity.edu.iq/id/eprint/2781 |
