期刊
MOLECULAR PHARMACEUTICS
卷 4, 期 5, 页码 652-658出版社
AMER CHEMICAL SOC
DOI: 10.1021/mp0700514
关键词
targeted therapy; cytotoxic peptide analogues; AN-152 [AEZS 108]; AN-207; AN238; AN-215; LHRH; somatostatin; bombesin
Gynecological cancers such as breast, ovarian, and endometrial carcinoma express receptors for luteinizing hormone-releasing hormone (LHRH), bombesin/gastrin-releasing peptide (BN/GRP), and somatostatin (SST). These tumors are therefore suitable candidates for targeted therapy with cytotoxic hybrid molecules consisting of a cytotoxic radical and a peptide hormone analogue as a carrier. These compounds have been shown to be more active and less toxic in vivo than nontargeted chemotherapy in models of various human cancers which express the respective receptors. The current review summarizes experimental and clinical findings with cytotoxic peptide hormone analogues of LHRH (AN-152 [AEZS 108], AN-207), BN/GRP (AN-215), and SST (AN-238) in breast, ovarian, and endometrial cancers.
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