Literature DB >> 17705441

Targeted therapy of breast and gynecological cancers with cytotoxic analogues of peptide hormones.

Jörg B Engel1, Andrew V Schally, Johannes Dietl, Lorenz Rieger, Arnd Hönig.   

Abstract

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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Year:  2007        PMID: 17705441     DOI: 10.1021/mp0700514

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  15 in total

1.  GnRH-R-Targeted Lytic Peptide Sensitizes BRCA Wild-type Ovarian Cancer to PARP Inhibition.

Authors:  Shaolin Ma; Sunila Pradeep; Alejandro Villar-Prados; Yunfei Wen; Emine Bayraktar; Lingegowda S Mangala; Mark Seungwook Kim; Sherry Y Wu; Wei Hu; Cristian Rodriguez-Aguayo; Carola Leuschner; Xiaoyan Liang; Prahlad T Ram; Katharina Schlacher; Robert L Coleman; Anil K Sood
Journal:  Mol Cancer Ther       Date:  2019-03-29       Impact factor: 6.261

2.  Receptors for luteinizing hormone-releasing hormone (GnRH) as therapeutic targets in triple negative breast cancers (TNBC).

Authors:  C W Kwok; O Treeck; S Buchholz; S Seitz; O Ortmann; J B Engel
Journal:  Target Oncol       Date:  2014-10-09       Impact factor: 4.493

Review 3.  Targeting GRPR in urological cancers--from basic research to clinical application.

Authors:  Rosalba Mansi; Achim Fleischmann; Helmut R Mäcke; Jean C Reubi
Journal:  Nat Rev Urol       Date:  2013-03-19       Impact factor: 14.432

Review 4.  Bombesin-related peptides and their receptors: recent advances in their role in physiology and disease states.

Authors:  Nieves Gonzalez; Terry W Moody; Hisato Igarashi; Tetsuhide Ito; Robert T Jensen
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2008-02       Impact factor: 3.243

Review 5.  International Union of Pharmacology. LXVIII. Mammalian bombesin receptors: nomenclature, distribution, pharmacology, signaling, and functions in normal and disease states.

Authors:  R T Jensen; J F Battey; E R Spindel; R V Benya
Journal:  Pharmacol Rev       Date:  2007-11-30       Impact factor: 25.468

6.  Linker stability influences the anti-tumor activity of acetazolamide-drug conjugates for the therapy of renal cell carcinoma.

Authors:  Samuele Cazzamalli; Alberto Dal Corso; Dario Neri
Journal:  J Control Release       Date:  2016-11-24       Impact factor: 9.776

7.  Intracellular delivery of an antisense oligonucleotide via endocytosis of a G protein-coupled receptor.

Authors:  Xin Ming; Md Rowshon Alam; Michael Fisher; Yongjun Yan; Xiaoyuan Chen; Rudolph L Juliano
Journal:  Nucleic Acids Res       Date:  2010-06-15       Impact factor: 16.971

8.  TumorHoPe: a database of tumor homing peptides.

Authors:  Pallavi Kapoor; Harinder Singh; Ankur Gautam; Kumardeep Chaudhary; Rahul Kumar; Gajendra P S Raghava
Journal:  PLoS One       Date:  2012-04-16       Impact factor: 3.240

9.  Triple negative breast cancers express receptors for LHRH and are potential therapeutic targets for cytotoxic LHRH-analogs, AEZS 108 and AEZS 125.

Authors:  Stephan Seitz; Stefan Buchholz; Andrew Victor Schally; Florian Weber; Monika Klinkhammer-Schalke; Elisabeth C Inwald; Roberto Perez; Ferenc G Rick; Luca Szalontay; Florian Hohla; Sabine Segerer; Chui Wai Kwok; Olaf Ortmann; Jörg Bernhard Engel
Journal:  BMC Cancer       Date:  2014-11-19       Impact factor: 4.430

10.  Targeted cytotoxic analog of luteinizing hormone-releasing hormone (LHRH), AEZS-108 (AN-152), inhibits the growth of DU-145 human castration-resistant prostate cancer in vivo and in vitro through elevating p21 and ROS levels.

Authors:  Petra Popovics; Andrew V Schally; Luca Szalontay; Norman L Block; Ferenc G Rick
Journal:  Oncotarget       Date:  2014-06-30
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