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Updated: Jul 8, 2026

MR Molecular Imaging of Prostate Cancer with a Small Molecular CLT1 Peptide Targeted Contrast Agent
Published on: September 3, 2013
New treatment approaches for prostate cancer based on peptide analogues
Anton Stangelberger1, Andrew V Schally, Bob Djavan
1Department of Urology University of Vienna, Vienna, Austria.
Objectives:
New therapy modalities for the treatment of advanced prostate cancer based on peptide analogues are reviewed.
Results:
Agonists and antagonists of luteinising hormone-releasing hormone (LHRH) lead to androgen deprivation, but direct effects on tumours may also play a role. Radiolabeled somatostatin analogues can be targeted to tumours expressing receptors for somatostatin and have been successfully applied for the localization of these tumours. Tumoural LHRH, growth hormone-releasing hormone (GHRH), and bombesin/gastrin-releasing peptide (BN/GRP) and their receptors appear to be involved in the proliferation of prostate cancer. On the basis of the recent advances in the understanding of the role of neuropeptides in tumour growth and progression, new therapeutic modalities are being developed that are based on antagonists of GHRH and of BN/GRP, which inhibit growth factors or their receptors. Another promising approach for the therapy of prostate cancer consists of the use of cytotoxic analogues of LHRH, bombesin, and somatostatin, which can be targeted to receptors for these peptides in prostate cancers and their metastases.
Conclusions:
New promising forms of hormone therapy and targeted chemotherapy may improve therapy of advanced stage prostate cancer.
Insights
New peptide analogue therapies, including luteinising hormone-releasing hormone (LHRH) and somatostatin analogues, show promise for advanced prostate cancer. These targeted treatments offer new avenues for hormone therapy and chemotherapy.
Area of Science:
- Oncology
- Endocrinology
- Peptide Therapeutics
Background:
- Advanced prostate cancer treatment remains a challenge.
- Neuropeptides and their receptors play a role in prostate cancer proliferation and progression.
Purpose of the Study:
- To review novel therapeutic strategies for advanced prostate cancer utilizing peptide analogues.
- To explore the potential of targeting specific peptide receptors on cancer cells.
Main Methods:
- Review of current literature on peptide analogue therapies.
- Analysis of the role of luteinising hormone-releasing hormone (LHRH), somatostatin, growth hormone-releasing hormone (GHRH), and bombesin/gastrin-releasing peptide (BN/GRP) pathways.
Main Results:
- LHRH analogues induce androgen deprivation, with potential direct anti-tumour effects.
- Radiolabeled somatostatin analogues aid in tumour localization.
- GHRH and BN/GRP antagonists, along with cytotoxic peptide analogues, are emerging as promising therapeutic agents.
Conclusions:
- Targeted therapies using peptide analogues represent a significant advancement in treating advanced prostate cancer.
- These novel approaches may enhance hormone therapy and enable targeted chemotherapy for improved patient outcomes.
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