Suitability of GnRH Receptors for Targeted Photodynamic Therapy in Head and Neck Cancers

被引:7
|
作者
Petho, Lilla [1 ]
Muranyi, Jozsef [2 ]
Penzes, Kinga [2 ]
Gurbi, Bianka [2 ]
Brauswetter, Diana [2 ]
Halmos, Gabor [3 ]
Csik, Gabriella [4 ]
Mezo, Gabor [1 ,5 ]
机构
[1] MTA ELTE Res Grp Peptide Chem, H-1117 Budapest, Hungary
[2] MTA SE Pathobiochem Res Grp, H-1094 Budapest, Hungary
[3] Univ Debrecen, Dept Biopharm, Fac Pharm, H-4032 Debrecen, Hungary
[4] SE Dept Biophys & Radiat Biol, H-1094 Budapest, Hungary
[5] Eotvos Lorand Univ, Inst Chem, Dept Organ Chem, Fac Sci, H-1117 Budapest, Hungary
关键词
GnRH-R; GnRH; protoporphyrin; targeted drug delivery; conjugate; photodynamic therapy; head and neck cancer; GONADOTROPIN-RELEASING-HORMONE; GROWTH-FACTOR RECEPTOR; ANTITUMOR-ACTIVITY; PROTOPORPHYRIN IX; CYTOTOXIC ANALOGS; DOXORUBICIN; BREAST; AN-152; ACID; GENE;
D O I
10.3390/ijms20205027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Head and neck squamous cell carcinomas (HNSCC) have a high mortality rate, although several potential therapeutic targets have already been identified. Gonadotropin-releasing hormone receptor (GnRH-R) expression is less studied in head and neck cancers, hence, we investigated the therapeutic relevance of GnRH-R targeting in HNSCC patients. Our results indicate that half of the patient-derived samples showed high GnRH-R expression, which was associated with worse prognosis, making this receptor a promising target for GnRH-based drug delivery. Photodynamic therapy is a clinically approved treatment for HNSCC, and the efficacy and selectivity may be enhanced by the covalent conjugation of the photosensitizer to a GnRH-R targeting peptide. Several native ligands, gonadotropin-releasing hormone (GnRH) isoforms, are known to target GnRH-R effectively. Therefore, different (4)Lys(Bu) modified GnRH analogs were designed and conjugated to protoporphyrin IX. The receptor binding potency of the novel conjugates was measured on human pituitary and human prostate cancer cells, indicating only slightly lower GnRH-R affinity than the peptides. The in vitro cell viability inhibition was tested on Detroit-562 human pharyngeal carcinoma cells that express GnRH-R in high levels, and the results showed that all conjugates were more effective than the free protoporphyrin IX.
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页数:17
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