TISSUE PLATELET DERIVED-GROWTH FACTOR (PDGF) PREDICTS FOR SHORTENED SURVIVAL AND TREATMENT FAILURE IN ADVANCED BREAST-CANCER

被引:85
作者
SEYMOUR, L [1 ]
DAJEE, D [1 ]
BEZWODA, WR [1 ]
机构
[1] UNIV WITWATERSRAND,SCH MED,DEPT MED,DIV CLIN HAEMATOL & MED ONCOL,YORK RD,JOHANNESBURG 2193,SOUTH AFRICA
关键词
PLATELET DERIVED GROWTH FACTOR; BREAST CANCER; IMMUNOHISTOCHEMISTRY; PROGNOSIS; TUMOR PROGRESSION;
D O I
10.1007/BF00665802
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In a study of plasma and tissue platelet derived growth factor (PDGF) concentration in patients with breast cancer, elevated levels of plasma PDGF were found in a significant proportion, 11/37 (30%), of patients. Sixteen patients (43%) had tumors which expressed PDGF-AA and 6 patients had tumors which in addition expressed the BB isoform of PDGF. All patients with elevated plasma levels of platelet derived growth factor had tumors which expressed the growth factor on immunohistochemical staining of tumor cells. Furthermore there was a significant correlation between plasma levels of platelet derived growth factor and the intensity of tissue staining. Patients With stage four breast cancer with tumors which were positive for platelet derived growth factor had a significantly lower response rate to chemotherapy as well as significantly shorter duration of survival. In addition, patients with stage four breast cancer who had elevated plasma PDGF levels had a significantly shorter survival. These results indicate that elevated plasma levels of platelet derived growth factor in patients with breast cancer are derived from the tumor cells and suggest that platelet derived growth factor may play a significant role in control tumor cell growth.
引用
收藏
页码:247 / 252
页数:6
相关论文
共 12 条
[1]   PLATELET-DERIVED GROWTH-FACTOR (PDGF) IN PLASMA OF BREAST-CANCER PATIENTS - CORRELATION WITH STAGE AND RATE OF PROGRESSION [J].
ARIAD, S ;
SEYMOUR, L ;
BEZWODA, WR .
BREAST CANCER RESEARCH AND TREATMENT, 1991, 20 (01) :11-17
[2]   SYNTHESIS AND SECRETION OF PLATELET-DERIVED GROWTH-FACTOR BY HUMAN-BREAST CANCER CELL-LINES [J].
BRONZERT, DA ;
PANTAZIS, P ;
ANTONIADES, HN ;
KASID, A ;
DAVIDSON, N ;
DICKSON, RB ;
LIPPMAN, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (16) :5763-5767
[3]  
DEINHARDT F, 1980, VIRAL ONCOLOGY
[4]  
HELDIN C-H, 1986, Cancer Reviews, V2, P34
[5]   EXPRESSION OF SEVERAL GROWTH-FACTORS AND THEIR RECEPTOR GENES IN HUMAN COLON CARCINOMAS [J].
ITO, M ;
YOSHIDA, K ;
KYO, E ;
AYHAN, A ;
NAKAYAMA, H ;
YASUI, W ;
ITO, H ;
TAHARA, E .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1990, 59 (03) :173-178
[6]   EXPRESSION OF MESSENGER-RNAS FOR PLATELET-DERIVED GROWTH-FACTOR AND ITS RECEPTORS IN HUMAN SARCOMA CELL-LINES [J].
LEVEEN, P ;
CLAESSONWELSH, L ;
HELDIN, CH ;
WESTERMARK, B ;
BETSHOLTZ, C .
INTERNATIONAL JOURNAL OF CANCER, 1990, 46 (06) :1066-1070
[7]   GROWTH-REGULATION OF HUMAN-BREAST CARCINOMA OCCURS THROUGH REGULATED GROWTH-FACTOR SECRETION [J].
LIPPMAN, ME ;
DICKSON, RB ;
GELMANN, EP ;
ROSEN, N ;
KNABBE, C ;
BATES, S ;
BRONZERT, D ;
HUFF, K ;
KASID, A .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1987, 35 (01) :1-16
[8]   EARLY PRESENCE OF ACTIVATED (EXHAUSTED) PLATELETS IN MALIGNANT-TUMORS (BREAST ADENOCARCINOMA AND MALIGNANT-MELANOMA) [J].
MANNUCCI, PM ;
CATTANEO, M ;
CANCIANI, MT ;
MANIEZZO, M ;
VAGLINI, M ;
CASCINELLI, N .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1989, 25 (10) :1413-1417
[9]  
PANTAZIS P, 1990, EUR J HAEMATOL, V45, P127
[10]  
PEROSIO PM, 1989, LAB INVEST, V60, P245