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PMID: 6378376 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Lack of effect of in vivo prostacyclin on the development of pulmonary metastases in mice following intravenous injection of CT26 colon carcinoma, Lewis lung carcinoma, or B16 amelanotic melanoma cells.

Cancer research ·Vol. 44 ·No. 9 ·1984-09-00 ·Pages 3880-3

Karpatkin S, Ambrogio C, Pearlstein E

Abstract

Honn et al. [Science (Wash. DC), 212: 1270, 1981] have recently reported a 93% reduction in the development of metastases of B16 amelanotic tumor cells given i.v. following a single dose of prostacyclin (PGI2) (100 micrograms) and theophylline (100 micrograms) 30 min prior to the injection of tumor cells. We have been unable to reduce pulmonary metastases induced by the i.v. injection of CT26 colon adenocarcinoma, Lewis lung carcinoma, or B16 amelanotic melanoma cells with a similar regimen. Thus, PGI2 and theophylline given prior to injection of tumor cells and 2 hr postinjection had no effect on the number or volume of pulmonary tumor nodules for CT26 cells, using 15 experimental and 14 control animals; Lewis lung cells, using 14 experimental and 13 control animals; or B16 amelanotic cells, using 26 experimental and 12 control animals. The PGI2 used was shown to be active in vitro, inhibiting tumor-induced platelet aggregation by all three tumors at 10(-9)M; and in vivo by inhibition of Lewis lung-induced thrombocytopenia at 1 hr, using 100 micrograms PGI2 prior to the injection of tumor cells.

MeSH Terms
Animals Cell Line Colonic Neoplasms/pathology Epoprostenol/pharmacology Lung Neoplasms/pathology,secondary Melanoma/pathology,secondary Mice Platelet Aggregation/drug effects Theophylline/pharmacology Time Factors
Chemicals
Theophylline Epoprostenol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Karpatkin S
Ambrogio C
Pearlstein E
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1984-09-00
Pages
3880-3
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NIADDK NIH HHS · AM 01431 · United States
NHLBI NIH HHS · NHLBI 13336-13 · United States
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