Imaging of bioluminescent LNCaP-luc-M6 Tumors: A new animal model for the study of metastatic human prostate cancer

BACKGROUND Animal experiments examining hormone‐sensitive metastatic prostate cancer using the human LNCaP cell line have been limited to endpoint analyses. To permit longitudinal studies, we generated a luciferase‐expressing cell line and used bioluminescent imaging (BLI) to non‐invasively monitor...

Full description

Saved in:
Bibliographic Details
Published in:The Prostate Vol. 59; no. 3; pp. 292 - 303
Main Authors: Scatena, Caroline D., Hepner, Mischa A., Oei, Yoko A., Dusich, Joan M., Yu, Shang-Fan, Purchio, Tony, Contag, Pamela R., Jenkins, Darlene E.
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15-05-2004
Wiley-Liss
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:BACKGROUND Animal experiments examining hormone‐sensitive metastatic prostate cancer using the human LNCaP cell line have been limited to endpoint analyses. To permit longitudinal studies, we generated a luciferase‐expressing cell line and used bioluminescent imaging (BLI) to non‐invasively monitor the in vivo growth of primary LNCaP tumors and metastasis. METHODS LNCaP.FGC cells were transfected to constitutively express firefly luciferase. LNCaP‐luc‐M6 cells were tested for bioluminescent signal intensity and hormone responsiveness in vitro. The cells were implanted in subcutaneous and orthotopic sites in SCID‐bg mice and imaged over time. RESULTS The LNCaP‐luc‐M6 cells formed subcutaneous and orthotopic tumors in SCID‐bg mice, and nearly all tumor‐bearing animals developed pulmonary metastases. Early detection and temporal growth of primary tumors and metastatic lesions was successfully monitored by BLI. CONCLUSIONS The LNCaP‐luc‐M6 cell line is a bioluminescent, hormone‐sensitive prostate cancer cell line applicable for BLI studies to non‐invasively monitor subcutaneous and orthotopic prostate tumor growth and metastasis in vivo. © 2004 Wiley‐Liss, Inc.
Bibliography:ArticleID:PROS20003
ark:/67375/WNG-H8S4P0X1-Q
istex:62B5425563F309C7A2A2A51E464D8D2CDFDEFCD3
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0270-4137
1097-0045
DOI:10.1002/pros.20003