A New Peptide Ligand for Targeting Human Carbonic Anhydrase IX, Identified through the Phage Display Technology

被引:26
作者
Askoxylakis, Vasileios [1 ]
Garcia-Boy, Regine [2 ]
Rana, Shoaib [2 ]
Kraemer, Susanne [2 ]
Hebling, Ulrike [2 ]
Mier, Walter [2 ]
Altmann, Annette [3 ]
Markert, Annette [3 ]
Debus, Juergen [1 ]
Haberkorn, Uwe [2 ,3 ]
机构
[1] Univ Heidelberg, Dept Radiooncol & Radiat Therapy, Heidelberg, Germany
[2] Univ Heidelberg, Dept Nucl Med, Heidelberg, Germany
[3] German Canc Res Ctr, Clin Cooperat Unit Nucl Med, D-6900 Heidelberg, Germany
来源
PLOS ONE | 2010年 / 5卷 / 12期
关键词
ENDOTHELIAL GROWTH-FACTOR; SQUAMOUS-CELL CARCINOMA; TUMOR HYPOXIA; POOR-PROGNOSIS; LUNG-CANCER; NECK-CANCER; EXPRESSION; MARKER; HYPOXIA-INDUCIBLE-FACTOR-1-ALPHA; THERAPEUTICS;
D O I
10.1371/journal.pone.0015962
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Carbonic anhydrase IX (CAIX) is a transmembrane enzyme found to be overexpressed in various tumors and associated with tumor hypoxia. Ligands binding this target may be used to visualize hypoxia, tumor manifestation or treat tumors by endoradiotherapy. Methods: Phage display was performed with a 12 amino acid phage display library by panning against a recombinant extracellular domain of human carbonic anhydrase IX. The identified peptide CaIX-P1 was chemically synthesized and tested in vitro on various cell lines and in vivo in Balb/c nu/nu mice carrying subcutaneously transplanted tumors. Binding, kinetic and competition studies were performed on the CAIX positive human renal cell carcinoma cell line SKRC 52, the CAIX negative human renal cell carcinoma cell line CaKi 2, the human colorectal carcinoma cell line HCT 116 and on human umbilical vein endothelial cells (HUVEC). Organ distribution studies were carried out in mice, carrying SKRC 52 tumors. RNA expression of CAIX in HCT 116 and HUVEC cells was investigated by quantitative real time PCR. Results: In vitro binding experiments of (125)I-labeled-CaIX-P1 revealed an increased uptake of the radioligand in the CAIX positive renal cell carcinoma cell line SKRC 52. Binding of the radioligand in the colorectal carcinoma cell line HCT 116 increased with increasing cell density and correlated with the mRNA expression of CAIX. Radioligand uptake was inhibited up to 90% by the unlabeled CaIX-P1 peptide, but not by the negative control peptide octreotide at the same concentration. No binding was demonstrated in CAIX negative CaKi 2 and HUVEC cells. Organ distribution studies revealed a higher accumulation in SKRC 52 tumors than in heart, spleen, liver, muscle, intestinum and brain, but a lower uptake compared to blood and kidney. Conclusions: These data indicate that CaIX-P1 is a promising candidate for the development of new ligands targeting human carbonic anhydrase IX.
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页数:10
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