Christos Liolios*, George Laros, Kyriakos Georgiou and Antonios Kolokouris*,
{"title":"靶向前列腺特异性膜抗原治疗前列腺癌的前药","authors":"Christos Liolios*, George Laros, Kyriakos Georgiou and Antonios Kolokouris*, ","doi":"10.1021/acs.jmedchem.4c02626","DOIUrl":null,"url":null,"abstract":"<p >Prostate-specific membrane antigen (PSMA) or glutamate carboxypeptidase II (GCPII) is a promising target for metastatic castration-resistant prostate cancer (mCRPC) due to its high expression in prostate cancer cell membranes and low expression in normal tissues. Ligand-targeted drugs (LTDs) targeting PSMA are gaining popularity for their high affinity, specificity, and ease of synthesis. LTDs consist of a small molecule targeting PSMA and carrying the cytotoxic agent to the cancer cells, which is then released through a cleavable linker (enzymatically or chemically cleaved) into the tumor tissue. Several PSMA-targeting LTDs have demonstrated promising results in both <i>in vitro</i> and <i>in vivo</i> studies, and a few are in clinical trials, showing potential to outperform the unmodified cytotoxic drugs. This article focuses on their structures and preclinical studies while discussing clinical data for a few very promising PSMA-targeting LTDs in detail.</p>","PeriodicalId":46,"journal":{"name":"Journal of Medicinal Chemistry","volume":"68 12","pages":"12296–12330"},"PeriodicalIF":6.8000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.4c02626","citationCount":"0","resultStr":"{\"title\":\"Prodrugs Targeting Prostate-Specific Membrane Antigen against Prostate Cancer\",\"authors\":\"Christos Liolios*, George Laros, Kyriakos Georgiou and Antonios Kolokouris*, \",\"doi\":\"10.1021/acs.jmedchem.4c02626\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Prostate-specific membrane antigen (PSMA) or glutamate carboxypeptidase II (GCPII) is a promising target for metastatic castration-resistant prostate cancer (mCRPC) due to its high expression in prostate cancer cell membranes and low expression in normal tissues. Ligand-targeted drugs (LTDs) targeting PSMA are gaining popularity for their high affinity, specificity, and ease of synthesis. LTDs consist of a small molecule targeting PSMA and carrying the cytotoxic agent to the cancer cells, which is then released through a cleavable linker (enzymatically or chemically cleaved) into the tumor tissue. Several PSMA-targeting LTDs have demonstrated promising results in both <i>in vitro</i> and <i>in vivo</i> studies, and a few are in clinical trials, showing potential to outperform the unmodified cytotoxic drugs. This article focuses on their structures and preclinical studies while discussing clinical data for a few very promising PSMA-targeting LTDs in detail.</p>\",\"PeriodicalId\":46,\"journal\":{\"name\":\"Journal of Medicinal Chemistry\",\"volume\":\"68 12\",\"pages\":\"12296–12330\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.4c02626\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medicinal Chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jmedchem.4c02626\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jmedchem.4c02626","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Prodrugs Targeting Prostate-Specific Membrane Antigen against Prostate Cancer
Prostate-specific membrane antigen (PSMA) or glutamate carboxypeptidase II (GCPII) is a promising target for metastatic castration-resistant prostate cancer (mCRPC) due to its high expression in prostate cancer cell membranes and low expression in normal tissues. Ligand-targeted drugs (LTDs) targeting PSMA are gaining popularity for their high affinity, specificity, and ease of synthesis. LTDs consist of a small molecule targeting PSMA and carrying the cytotoxic agent to the cancer cells, which is then released through a cleavable linker (enzymatically or chemically cleaved) into the tumor tissue. Several PSMA-targeting LTDs have demonstrated promising results in both in vitro and in vivo studies, and a few are in clinical trials, showing potential to outperform the unmodified cytotoxic drugs. This article focuses on their structures and preclinical studies while discussing clinical data for a few very promising PSMA-targeting LTDs in detail.
期刊介绍:
The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents.
The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.