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Quantitative and qualitative differences in growth, invasion and lung colonization of an anaplastic and a papillary human thyroid cancer cell linein vitro andin vivo
Authors:Erwin R. Boghaert  Kenneth Ain  Kimberly Taylor  Victoria L. Greenberg  Carol Fowler  Stephen G. Zimmer
Affiliation:(1) Department of Surgery, University of Kentucky Medical Center, Lexington, KY, USA;(2) Medical Service, Veterans Affairs Medical Center, and the Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY, USA;(3) Department of Microbiology & Immunology, University of Kentucky Medical Center, Lexington, KY, USA;(4) Lucille Parker Markey Cancer Center, Lexington, KY, USA;(5) Lucille Parker Markey Cancer Center, Rm 317, Combs Building, 800 Rose Street, 40536-0093 Lexington, KY, USA
Abstract:Invasion and metastasis remain major reasons for failure of anti-cancer therapy. Cell lines derived from human carcinomas are frequently used to investigate the molecular mechanisms that underlie invasion and metastasis. Unfortunately many of these cell lines do not retain the malignant characteristics of their parental tumors. We therefore conducted a series of experimentsin vivo andin vitro to identify which aspects of malignancy of a papillary (NPA'87) and an anaplastic (DR090-1) thyroid carcinoma were consistent with the pathology of the parental tumor types. We evaluated tumor growth, invasion and metastasis of DRO90-1 and NPA'87in vivo following inoculation of the tumor cells under the dermis, under the renal capsule and into the lateral tail vein of nude mice. This evaluationin vivo showed that the anaplastic carcinoma had a faster growth rate compared with the papillary carcinoma. Furthermore, the papillary carcinoma cells could destroy and infiltrate surrounding tissue but were not capable of extravasation and colonization of lung tissue. The anaplastic cells formed lung nodules following injection into the tail vein of nude mice. This lung colonizing capability of DR090-1 correlated with their capacity to secrete an active 62 kDa gelatinase and to migrate through reconstituted basement membranein vitro.
Keywords:basement membrane  gelatinase  invasion  thyroid cancer
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