Midkine is highly expressed in neuroblastoma tissues.

Standard

Midkine is highly expressed in neuroblastoma tissues. / Fiegel, Henning C; Kaifi, Jussuf; Wachowiak, Robin; Quaas, Alexander; Aridome, Kuniaki; Ichihara-Tanaka, Keiko; Muramatsu, Takashi; Metzger, Roman; Izbicki, Jakob R.; Erttmann, Rudolf; Kluth, Dietrich; Till, Holger.

in: PEDIATR SURG INT, Jahrgang 24, Nr. 12, 12, 2008, S. 1355-1359.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Fiegel, HC, Kaifi, J, Wachowiak, R, Quaas, A, Aridome, K, Ichihara-Tanaka, K, Muramatsu, T, Metzger, R, Izbicki, JR, Erttmann, R, Kluth, D & Till, H 2008, 'Midkine is highly expressed in neuroblastoma tissues.', PEDIATR SURG INT, Jg. 24, Nr. 12, 12, S. 1355-1359. <http://www.ncbi.nlm.nih.gov/pubmed/18956201?dopt=Citation>

APA

Fiegel, H. C., Kaifi, J., Wachowiak, R., Quaas, A., Aridome, K., Ichihara-Tanaka, K., Muramatsu, T., Metzger, R., Izbicki, J. R., Erttmann, R., Kluth, D., & Till, H. (2008). Midkine is highly expressed in neuroblastoma tissues. PEDIATR SURG INT, 24(12), 1355-1359. [12]. http://www.ncbi.nlm.nih.gov/pubmed/18956201?dopt=Citation

Vancouver

Fiegel HC, Kaifi J, Wachowiak R, Quaas A, Aridome K, Ichihara-Tanaka K et al. Midkine is highly expressed in neuroblastoma tissues. PEDIATR SURG INT. 2008;24(12):1355-1359. 12.

Bibtex

@article{a1bde54f0cc04d39b00f31d76cecbd1c,
title = "Midkine is highly expressed in neuroblastoma tissues.",
abstract = "PURPOSE: Neuroblastoma (NBL) is a tumor from neural crest cells, and is the most frequent solid tumor in children. Midkine (MK) is a pleiotropin analogon, which is frequently expressed in neuronal and epithelial tumors and is a marker for a poor clinical outcome. The aims of this study were to assess MK expression in NBL and investigate the correlation with clinical outcome. METHODS: Fifty-six specimens of NBL were stained for MK on a tissue microarray by immunohistochemistry (IHC). Fresh frozen tumor tissues were used for RNA isolation, and RT-PCR analysis for MK-mRNA expression was performed. Survival data, risk factors and disease stages were correlated with MK status assessed by IHC and RT-PCR analysis. RESULTS: MK-mRNA expression was found in the majority of the tumor tissues (75%), whereas MK protein could be detected only in 46% of the NBL by IHC. No correlation of MK status with survival, risk factors or disease stage was observed. CONCLUSION: A majority of NBL express MK-mRNA, whereas not all MK mRNA positive tumors showed also a positive MK IHC staining. The high expression of MK-mRNA expression might present a promising target for new adenovirus-based gene therapeutic approaches for the treatment of NBL.",
author = "Fiegel, {Henning C} and Jussuf Kaifi and Robin Wachowiak and Alexander Quaas and Kuniaki Aridome and Keiko Ichihara-Tanaka and Takashi Muramatsu and Roman Metzger and Izbicki, {Jakob R.} and Rudolf Erttmann and Dietrich Kluth and Holger Till",
year = "2008",
language = "Deutsch",
volume = "24",
pages = "1355--1359",
journal = "PEDIATR SURG INT",
issn = "0179-0358",
publisher = "Springer",
number = "12",

}

RIS

TY - JOUR

T1 - Midkine is highly expressed in neuroblastoma tissues.

AU - Fiegel, Henning C

AU - Kaifi, Jussuf

AU - Wachowiak, Robin

AU - Quaas, Alexander

AU - Aridome, Kuniaki

AU - Ichihara-Tanaka, Keiko

AU - Muramatsu, Takashi

AU - Metzger, Roman

AU - Izbicki, Jakob R.

AU - Erttmann, Rudolf

AU - Kluth, Dietrich

AU - Till, Holger

PY - 2008

Y1 - 2008

N2 - PURPOSE: Neuroblastoma (NBL) is a tumor from neural crest cells, and is the most frequent solid tumor in children. Midkine (MK) is a pleiotropin analogon, which is frequently expressed in neuronal and epithelial tumors and is a marker for a poor clinical outcome. The aims of this study were to assess MK expression in NBL and investigate the correlation with clinical outcome. METHODS: Fifty-six specimens of NBL were stained for MK on a tissue microarray by immunohistochemistry (IHC). Fresh frozen tumor tissues were used for RNA isolation, and RT-PCR analysis for MK-mRNA expression was performed. Survival data, risk factors and disease stages were correlated with MK status assessed by IHC and RT-PCR analysis. RESULTS: MK-mRNA expression was found in the majority of the tumor tissues (75%), whereas MK protein could be detected only in 46% of the NBL by IHC. No correlation of MK status with survival, risk factors or disease stage was observed. CONCLUSION: A majority of NBL express MK-mRNA, whereas not all MK mRNA positive tumors showed also a positive MK IHC staining. The high expression of MK-mRNA expression might present a promising target for new adenovirus-based gene therapeutic approaches for the treatment of NBL.

AB - PURPOSE: Neuroblastoma (NBL) is a tumor from neural crest cells, and is the most frequent solid tumor in children. Midkine (MK) is a pleiotropin analogon, which is frequently expressed in neuronal and epithelial tumors and is a marker for a poor clinical outcome. The aims of this study were to assess MK expression in NBL and investigate the correlation with clinical outcome. METHODS: Fifty-six specimens of NBL were stained for MK on a tissue microarray by immunohistochemistry (IHC). Fresh frozen tumor tissues were used for RNA isolation, and RT-PCR analysis for MK-mRNA expression was performed. Survival data, risk factors and disease stages were correlated with MK status assessed by IHC and RT-PCR analysis. RESULTS: MK-mRNA expression was found in the majority of the tumor tissues (75%), whereas MK protein could be detected only in 46% of the NBL by IHC. No correlation of MK status with survival, risk factors or disease stage was observed. CONCLUSION: A majority of NBL express MK-mRNA, whereas not all MK mRNA positive tumors showed also a positive MK IHC staining. The high expression of MK-mRNA expression might present a promising target for new adenovirus-based gene therapeutic approaches for the treatment of NBL.

M3 - SCORING: Zeitschriftenaufsatz

VL - 24

SP - 1355

EP - 1359

JO - PEDIATR SURG INT

JF - PEDIATR SURG INT

SN - 0179-0358

IS - 12

M1 - 12

ER -