Ursolic acid-induced changes in tumor growth, O2 consumption, and tumor interstitial fluid pressure

被引:3
作者
Lee, I
Lee, J
Lee, YH
Leonard, J
机构
[1] Univ Penn, Sch Med, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Coriell Inst Med Res, Camden, NJ 08103 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Radiat Res, Camden, NJ 08103 USA
关键词
triterpenoids; apoptosis; tumor blood flow;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The anti-tumor effect of ursolic acid (CA) and UA-induced changes in tumor physiology in tumor-bearing mice were examined. MTT colorimetric assay, clonogenic assay, and growth-delay assay for the determination of tumoricidal effects of UA were evaluated. UA-induced apoptosis was measured by fluorescent microscopy, stained by propidium iodide. Oxygen consumption (QO(2)) after treatment with UA was measured using a Clark-type electrode chamber. Systemic toxicity in mice was assayed by LD50(30). We also measured UA-induced changes in several tumor physiological parameters. Inhibitory effect of UA on various tumor cell lines was observed using MTT and clonogenic assays in vitro. UA-induced apoptosis significantly increased in a dose-dependent manner. Cellular QO(2) values were significantly reduced by UA. In animal studies, UA significantly reduced tumor interstitial fluid pressure (TIFP) to similar to 40% of the control values at 2-3 days post-treatment (P < 0.05). An i.p. administration of 100 mg/kg of UA significantly (P < 0.01) inhibited tumor growth of FSaII. In conclusion, UA showed anti-tumor effect on various tumor cells in vitro as well as a moderate retardation of growth in two tumor models in vivo. We gained some insight regarding the pathophysiological benefits of UA (i.e., reduction in TIFP) as a cancer therapeutic agent, Consequently, these observations can be used for further study of UA or to facilitate clinical applications of UA for treating cancer patients.
引用
收藏
页码:2827 / 2833
页数:7
相关论文
共 16 条
[1]
LACK OF GENERAL CORRELATION BETWEEN INTERSTITIAL FLUID PRESSURE AND OXYGEN PARTIAL-PRESSURE IN SOLID TUMORS [J].
BOUCHER, Y ;
LEE, I ;
JAIN, RK .
MICROVASCULAR RESEARCH, 1995, 50 (02) :175-182
[2]
Cha HJ, 1996, CANCER RES, V56, P2281
[3]
Cyclic adenosine monophosphate inhibits ursolic acid-induced apoptosis via activation of protein kinase A in human leukaemic HL-60 cells [J].
Choi, BM ;
Park, R ;
Pae, HO ;
Yoo, JC ;
Kim, YC ;
Jun, CD ;
Jung, BH ;
Oh, GS ;
So, HS ;
Kim, YM ;
Chung, HT .
PHARMACOLOGY & TOXICOLOGY, 2000, 86 (02) :53-58
[4]
ElSaady D, 1996, ANTICANCER RES, V16, P481
[5]
ANGIOGENIC FACTORS [J].
FOLKMAN, J ;
KLAGSBRUN, M .
SCIENCE, 1987, 235 (4787) :442-447
[6]
Effects of oleanolic acid and ursolic acid on inhibiting tumor growth and enhancing the recovery of hematopoietic system postirradiation in mice [J].
Hsu, HY ;
Yang, JJ ;
Lin, CC .
CANCER LETTERS, 1997, 111 (1-2) :7-13
[7]
BARRIERS TO DRUG-DELIVERY IN SOLID TUMORS [J].
JAIN, RK .
SCIENTIFIC AMERICAN, 1994, 271 (01) :58-65
[8]
Lee I, 2000, ANTICANCER RES, V20, P1037
[9]
EFFECT OF HEMODILUTION AND RESUSCITATION ON TUMOR INTERSTITIAL FLUID PRESSURE, BLOOD-FLOW, AND OXYGENATION [J].
LEE, I ;
DEMHARTNER, TJ ;
BOUCHER, Y ;
JAIN, RK ;
INTAGLIETTA, M .
MICROVASCULAR RESEARCH, 1994, 48 (01) :1-12
[10]
LEUNIG M, 1992, CANCER RES, V52, P6553