Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer.

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Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer. / Nitzsche, B; Gloesenkamp, C; Schrader, M; Hoffmann, B; Zengerling, F; Balabanov, S; Honecker, Friedemann; Höpfner, M.

In: BRIT J CANCER, Vol. 107, No. 11, 11, 2012, p. 1853-1863.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Nitzsche, B, Gloesenkamp, C, Schrader, M, Hoffmann, B, Zengerling, F, Balabanov, S, Honecker, F & Höpfner, M 2012, 'Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer.', BRIT J CANCER, vol. 107, no. 11, 11, pp. 1853-1863. <http://www.ncbi.nlm.nih.gov/pubmed/23169338?dopt=Citation>

APA

Nitzsche, B., Gloesenkamp, C., Schrader, M., Hoffmann, B., Zengerling, F., Balabanov, S., Honecker, F., & Höpfner, M. (2012). Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer. BRIT J CANCER, 107(11), 1853-1863. [11]. http://www.ncbi.nlm.nih.gov/pubmed/23169338?dopt=Citation

Vancouver

Nitzsche B, Gloesenkamp C, Schrader M, Hoffmann B, Zengerling F, Balabanov S et al. Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer. BRIT J CANCER. 2012;107(11):1853-1863. 11.

Bibtex

@article{bd0bed4d0047406eba39f96ebb8852fd,
title = "Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer.",
abstract = "Resistance to cisplatin-based chemotherapy is associated with poor prognosis in testicular germ cell cancer, emphasising the need for new therapeutic approaches. In this respect, the therapeutic concept of anti-angiogenesis is of particular interest. In a previous study, we presented two novel anti-angiogenic compounds, HP-2 and HP-14, blocking the tyrosine kinase activity of angiogenic growth factor receptors, such as vascular endothelial growth factor receptor-2 (VEGFR-2), and related signalling pathways in testicular cancer. In this study, we investigated the efficacy of these new compounds in platinum-resistant testicular germ cell tumours (TGCTs), in vitro and in vivo.",
keywords = "Animals, Humans, Male, Cell Line, Tumor, Gene Expression Profiling, Drug Resistance, Neoplasm, Cell Cycle/drug effects, Cisplatin/*therapeutic use, Antineoplastic Agents/*pharmacology, Chick Embryo, Angiogenesis Inhibitors/*pharmacology, Neoplasms, Germ Cell and Embryonal/*drug therapy/pathology, Neovascularization, Pathologic/drug therapy, Testicular Neoplasms/*drug therapy/pathology, Vascular Endothelial Growth Factor Receptor-2/analysis, Animals, Humans, Male, Cell Line, Tumor, Gene Expression Profiling, Drug Resistance, Neoplasm, Cell Cycle/drug effects, Cisplatin/*therapeutic use, Antineoplastic Agents/*pharmacology, Chick Embryo, Angiogenesis Inhibitors/*pharmacology, Neoplasms, Germ Cell and Embryonal/*drug therapy/pathology, Neovascularization, Pathologic/drug therapy, Testicular Neoplasms/*drug therapy/pathology, Vascular Endothelial Growth Factor Receptor-2/analysis",
author = "B Nitzsche and C Gloesenkamp and M Schrader and B Hoffmann and F Zengerling and S Balabanov and Friedemann Honecker and M H{\"o}pfner",
year = "2012",
language = "English",
volume = "107",
pages = "1853--1863",
journal = "BRIT J CANCER",
issn = "0007-0920",
publisher = "NATURE PUBLISHING GROUP",
number = "11",

}

RIS

TY - JOUR

T1 - Anti-tumour activity of two novel compounds in cisplatin-resistant testicular germ cell cancer.

AU - Nitzsche, B

AU - Gloesenkamp, C

AU - Schrader, M

AU - Hoffmann, B

AU - Zengerling, F

AU - Balabanov, S

AU - Honecker, Friedemann

AU - Höpfner, M

PY - 2012

Y1 - 2012

N2 - Resistance to cisplatin-based chemotherapy is associated with poor prognosis in testicular germ cell cancer, emphasising the need for new therapeutic approaches. In this respect, the therapeutic concept of anti-angiogenesis is of particular interest. In a previous study, we presented two novel anti-angiogenic compounds, HP-2 and HP-14, blocking the tyrosine kinase activity of angiogenic growth factor receptors, such as vascular endothelial growth factor receptor-2 (VEGFR-2), and related signalling pathways in testicular cancer. In this study, we investigated the efficacy of these new compounds in platinum-resistant testicular germ cell tumours (TGCTs), in vitro and in vivo.

AB - Resistance to cisplatin-based chemotherapy is associated with poor prognosis in testicular germ cell cancer, emphasising the need for new therapeutic approaches. In this respect, the therapeutic concept of anti-angiogenesis is of particular interest. In a previous study, we presented two novel anti-angiogenic compounds, HP-2 and HP-14, blocking the tyrosine kinase activity of angiogenic growth factor receptors, such as vascular endothelial growth factor receptor-2 (VEGFR-2), and related signalling pathways in testicular cancer. In this study, we investigated the efficacy of these new compounds in platinum-resistant testicular germ cell tumours (TGCTs), in vitro and in vivo.

KW - Animals

KW - Humans

KW - Male

KW - Cell Line, Tumor

KW - Gene Expression Profiling

KW - Drug Resistance, Neoplasm

KW - Cell Cycle/drug effects

KW - Cisplatin/therapeutic use

KW - Antineoplastic Agents/pharmacology

KW - Chick Embryo

KW - Angiogenesis Inhibitors/pharmacology

KW - Neoplasms, Germ Cell and Embryonal/drug therapy/pathology

KW - Neovascularization, Pathologic/drug therapy

KW - Testicular Neoplasms/drug therapy/pathology

KW - Vascular Endothelial Growth Factor Receptor-2/analysis

KW - Animals

KW - Humans

KW - Male

KW - Cell Line, Tumor

KW - Gene Expression Profiling

KW - Drug Resistance, Neoplasm

KW - Cell Cycle/drug effects

KW - Cisplatin/therapeutic use

KW - Antineoplastic Agents/pharmacology

KW - Chick Embryo

KW - Angiogenesis Inhibitors/pharmacology

KW - Neoplasms, Germ Cell and Embryonal/drug therapy/pathology

KW - Neovascularization, Pathologic/drug therapy

KW - Testicular Neoplasms/drug therapy/pathology

KW - Vascular Endothelial Growth Factor Receptor-2/analysis

M3 - SCORING: Journal article

VL - 107

SP - 1853

EP - 1863

JO - BRIT J CANCER

JF - BRIT J CANCER

SN - 0007-0920

IS - 11

M1 - 11

ER -