The effect of keratinocyte growth factor on tumour growth and small intestinal mucositis after chemotherapy in the rat with breast cancer

被引:82
作者
Gibson, RJ
Keefe, DMK
Clarke, JM
Regester, GO
Thompson, FM
Goland, GJ
Edwards, BG
Cummins, AG
机构
[1] Royal Adelaide Hosp, Dept Med Oncol, Adelaide, SA 5000, Australia
[2] Queen Elizabeth Hosp, Dept Gastroenterol, Adelaide, SA, Australia
[3] Womens & Childrens Hosp, Child Hlth Res Ctr, Adelaide, SA, Australia
关键词
keratinocyte growth factor; chemotherapy; mucositis; breast cancer; rats;
D O I
10.1007/s00280-002-0460-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Mucositis from cancer chemotherapy is a common problem for which there is no definitive treatment. It produces significant morbidity and occasional mortality. Prevention and successful treatment could significantly enhance the quality of life of patients, and improve survival, however any potential preventative agent must not enhance tumour growth. The aims of this study were to assess the effect of keratinocyte growth factor (KGF) on breast tumour growth, and in preventing small intestinal mucositis induced by methotrexate (MTX). Methods: Tumour-bearing rats received KGF or saline for 5 days prior to either MTX or saline treatment, and were killed 24 h after the last MTX injection. The weights of the tumour, small and large intestines, and liver were recorded. Apoptosis was assessed by TUNEL assay in the tumour and jejunum. Intestinal morphometry was used to assess villus area, crypt length and mitotic crypt count. Tumour proliferation was assessed by mitotic count. Results: KGF increased the weight of the small intestine prior to chemotherapy but the weight was not maintained after chemotherapy. KGF synergized with MTX to increase apoptosis in both intestinal crypts and the breast cancer. KGF also reduced tumour size. Conclusions: We conclude that KGF had a modest effect on intestinal growth prior to chemotherapy. It did not protect the gut from mucositis, nor did it worsen morphometry. It reduced tumour size.
引用
收藏
页码:53 / 58
页数:6
相关论文
共 21 条
[1]   Expression of keratinocyte growth factor and its receptor in human breast cancer [J].
Bansal, GS ;
Cox, HC ;
Marsh, S ;
Gomm, J ;
Yiangou, C ;
Luqmani, Y ;
Coombes, RC ;
Johnston, CL .
BRITISH JOURNAL OF CANCER, 1997, 75 (11) :1567-1574
[2]  
Brauchle M, 1996, AM J PATHOL, V149, P521
[3]   QUANTITATIVE HISTOLOGICAL STUDY OF ENTEROPATHY ASSOCIATED WITH HIV-INFECTION [J].
CUMMINS, AG ;
LABROOY, JT ;
STANLEY, DP ;
ROWLAND, R ;
SHEARMAN, DJC .
GUT, 1990, 31 (03) :317-321
[4]  
Farrell CL, 1999, INT J RADIAT BIOL, V75, P609
[5]  
Farrell CL, 1998, CANCER RES, V58, P933
[6]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[7]   Apoptosis and the dilemma of cancer chemotherapy [J].
Hannun, YA .
BLOOD, 1997, 89 (06) :1845-1853
[8]   PERITZ F-TEST - BASIC PROGRAM OF A ROBUST MULTIPLE COMPARISON TEST FOR STATISTICAL-ANALYSIS OF ALL DIFFERENCES AMONG GROUP MEANS [J].
HARPER, JF .
COMPUTERS IN BIOLOGY AND MEDICINE, 1984, 14 (04) :437-445
[9]   KERATINOCYTE GROWTH-FACTOR INDUCES PROLIFERATION OF HEPATOCYTES AND EPITHELIAL-CELLS THROUGHOUT THE RAT GASTROINTESTINAL-TRACT [J].
HOUSLEY, RM ;
MORRIS, CF ;
BOYLE, W ;
RING, B ;
BILTZ, R ;
TARPLEY, JE ;
AUKERMAN, SL ;
DEVINE, PL ;
WHITEHEAD, RH ;
PIERCE, GF .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :1764-1777
[10]  
KEEFE DM, 1998, THESIS U ADELAIDE AD