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The significance of arginase I administration on the survival of mice bearing NS-1 myeloma cells. J Surg Res 2009 Jan;151(1):28-32

Date

04/09/2008

Pubmed ID

18394650

DOI

10.1016/j.jss.2007.12.771

Scopus ID

2-s2.0-57149116991 (requires institutional sign-in at Scopus site)   5 Citations

Abstract

BACKGROUND: Arginase I blood levels elevate in cancerous patients and correlate with cancer stages and poor prognosis. Since arginase is capable of enhancing cell growth, it is unclear whether its ominous effect on cancer progression is through the inhibition of immunity or through direct enhancement of cancer cell growth. We tried to clarify this question.

METHODS: NS-1 mouse myeloma cells were inoculated intraperitoneally (i.p.) into mice. Purified mouse arginase I was injected daily either intravenously (i.v.) or i.p. for 6 d. A tumor-only control group received i.p. tumor cells without arginase. The survival rates of all mice were recorded.

RESULTS: Survival rates were significantly lower in the i.v. group than in the i.p. group (P=0.017) or in the tumor-only control group (P=0.034). As spleen is readily exposed to i.v. arginase, its natural killer cells were studied and were found to have been significantly suppressed by arginase in vitro (P<0.005).

CONCLUSION: Our results indicate that the direct inhibition of the immune system by i.v. arginase is more significant in shortening the survival of tumor-bearing mice than localized (i.p.) arginase promotion of tumor cell growth. Thus, an elevation of arginase in a patient's blood is very harmful to the host immune system, e.g. splenic natural killer cells.

Author List

Wang SR, Hou S, Wang A, Chang YJ, Liu CT, Tsay GJ, Wei CC

Author

Fang Yao Stephen Hou PhD, MB(ASCP)QCYM, MLS(ASCPi) Clinical Assistant Professor in the Biomedical Sciences Laboratory Programs department at University of Wisconsin - Milwaukee




MESH terms used to index this publication - Major topics in bold

Animals
Arginase
Cell Line, Tumor
Cell Proliferation
Injections, Intraperitoneal
Injections, Intravenous
Killer Cells, Natural
Male
Mice
Mice, Inbred BALB C
Multiple Myeloma
Survival Rate