Human α-defensins HNPs-1,-2, and-3 in renal cell carcinoma -: Influences on tumor cell proliferation

被引:115
作者
Müller, CA
Markovic-Lipkovski, J
Klatt, T
Gamper, J
Schwarz, G
Beck, H
Deeg, M
Kalbacher, H
Widmann, S
Wessels, JT
Becker, V
Müller, GA
Flad, T
机构
[1] Univ Tubingen, Med Clin, Dept 2, Sect Transplantat Immunol & Immunohematol, D-72072 Tubingen, Germany
[2] Univ Belgrade, Inst Pathol, Fac Med, Belgrade, Yugoslavia
[3] Univ Gottingen, Ctr Internal Med, Dept Nephrol & Rheumatol, D-3400 Gottingen, Germany
[4] Univ Tubingen, Childrens Hosp, Tubingen, Germany
[5] Univ Tubingen, Med & Nat Sci Res Ctr, Tubingen, Germany
关键词
D O I
10.1016/S0002-9440(10)62558-8
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
The alpha-defensins human neutrophil peptides (HNPs)-1, -2, and -3 have been described as cytotoxic peptides with restricted expression in neutrophils and in some lymphocytes. In this study we report that HNPs-1, -2, and -3 are also expressed in renal cell carcinomas (RCCs). Several RCC lines were found to express mRNA as well as the specific peptides of HNP-1, -2, and -3 demonstrated by reverse transcriptase-polymerase chain reaction, mass spectrometric, and flow cytometric analyses. At physiological concentrations HNPs-1, -2, and -3 stimulated cell proliferation of selected RCC lines in vitro but at high concentrations were cytotoxic for all RCC lines tested. As in RCC lines, alpha-defensins were also detected in vivo in malignant epithelial cells of 31 RCC tissues in addition to their expected presence in neutrophils. In most RCC cases randomly, patchy immunostaining of alpha-defensins on epithelial cells surrounding neutrophils was seen, but in six tumors of higher grade malignancy all tumor cells were diffusely stained. Cellular necrosis observed in RCC tissues in association with extensive patches of HNP-1, -2, and -3, seemed to be related to high concentrations of alpha-defensins. The in vitro and in vivo findings suggest that alpha-defensins are frequent peptide constituents of malignant epithelial cells in RCC with a possible direct influence on tumor proliferation.
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页码:1311 / 1324
页数:14
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