|
|
||||||||
Ann Thorac Surg 2000;69:1010-1015
© 2000 The Society of Thoracic Surgeons
a Departments of General Surgery and Thoracic Surgery, Christian-Albrechts-University Hospital, Kiel, Germany
b Pathology, Christian-Albrechts-University Hospital, Kiel, Germany
Address reprint requests to Dr Boehle, Department of General Surgery and Thoracic Surgery, Christian-Albrechts-University Hospital Kiel, Arnold-Heller-Str 7, D-24105 Kiel, Germany
e-mail: boehle{at}allg-thorax-chir.uni-kiel.de
Background. Overall prognosis in human lung cancer is still poor. A highly reproducible, easy to perform in vivo model, which closely resembles the clinical features of advanced human lung cancer, is required for the evaluation of novel therapies.
Methods. Tumor cells, originated from a human adenocarcinoma, a squamous cell carcinoma, and an undifferentiated large cell carcinoma, were xenotransplanted heterotopically by subcutaneous and intravenous injection and compared with orthotopic intrapleural and intrapulmonary xenotransplantation by a facilitated engraftment procedure into SCID bg mice.
Results. Subcutaneous injection of tumor cells resulted in a 100% engraftment rate with establishment of solid tumors without clinically relevant metastases. Intravenous injection had poor engraftment rates by hematogenous spread. Depending on the cell line, a 80% to 100% engraftment rate in orthotopic xenotransplantation was achieved, resulting in a consistent pattern of mediastinal and bilateral pulmonary metastases.
Conclusions. The facilitated orthotopic xenotransplantation of human lung cancer is easy to perform and results in a reproducible in vivo model that closely resembles the clinical features of advanced human lung cancer. Consequently, this model appears suitable for in vivo evaluation of novel cancer therapies in preclinical tests.
This article has been cited by other articles:
![]() |
F. Pastorino, C. Brignole, D. Di Paolo, B. Nico, A. Pezzolo, D. Marimpietri, G. Pagnan, F. Piccardi, M. Cilli, R. Longhi, et al. Targeting Liposomal Chemotherapy via Both Tumor Cell-Specific and Tumor Vasculature-Specific Ligands Potentiates Therapeutic Efficacy. Cancer Res., October 15, 2006; 66(20): 10073 - 10082. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Onn, T. Isobe, S. Itasaka, W. Wu, M. S. O'Reilly, W. Ki Hong, I. J. Fidler, and R. S. Herbst Development of an Orthotopic Model to Study the Biology and Therapy of Primary Human Lung Cancer in Nude Mice Clin. Cancer Res., November 15, 2003; 9(15): 5532 - 5539. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Kurdow, A. S. Boehle, S. Haye, L. Boenicke, B. Schniewind, P. Dohrmann, and H. Kalthoff Ganciclovir prodrug therapy is effective in a murine xenotransplant model of human lung cancer Ann. Thorac. Surg., March 1, 2002; 73(3): 905 - 910. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. S. Boehle, B. Sipos, U. Kliche, H. Kalthoff, and P. Dohrmann Combretastatin A-4 prodrug inhibits growth of human non-small cell lung cancer in a murine xenotransplant model Ann. Thorac. Surg., May 1, 2001; 71(5): 1657 - 1665. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |