IMMUNOHISTOCHEMICAL STAINING OF HA-RAS ONCOGENE PRODUCT IN NORMAL, BENIGN, AND MALIGNANT HUMAN PANCREATIC TISSUES

被引:84
作者
SHIMIZU, M [1 ]
SAITOH, Y [1 ]
ITOH, H [1 ]
机构
[1] KOBE UNIV,SCH MED,DEPT PATHOL & SURG 1,KOBE 650,JAPAN
关键词
benign pancreatic tissue; Ha-ras oncogene product (p21); immunohistochemical staining; normal pancreatic tissue; pancreatic cancer;
D O I
10.1016/S0046-8177(96)90006-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We examined immunohistochemical staining with Ha-ras oncogene product in normal, benign, and malignant human pancreatic tissues. In cases of pancreatic cancer, its relation to histologic type was evaluated. Serous cystadenoma and atypical acinar cell nodules did not react with the Ha-ras oncogene product, and ductal cells and acinar cells in normal pancreas showed lower immunoreactivity than other benign or malignant lesions. However, the positive rate of islet cells in normal pancreas was almost the same in cases of pancreatic cancer. Strongest positivity was observed in cases of chronic pancreatitis, and islet cell tumors also showed high positive staining rates. In pancreatic cancer, the positive rate of well-differentiated adenocarcinomas was rather higher than that of poorly differentiated adenocarcinomas. Our study indicates that the Ha-ras oncogene p21 product does not correlate with neoplastic transformation in human pancreas, is not a useful marker for differentiating benign and malignant lesions, and cannot be used to determine the origin of differentiation in the pancreas. © 1990.
引用
收藏
页码:607 / 612
页数:6
相关论文
共 35 条
[1]   IMMUNOHISTOCHEMICAL STAINING OF COLORECTAL TISSUES WITH MONOCLONAL-ANTIBODIES TO RAS ONCOGENE P21 PRODUCT AND CARBOHYDRATE DETERMINANT ANTIGEN 19-9 [J].
ALLEN, DC ;
FOSTER, H ;
ORCHIN, JC ;
BIGGART, JD .
JOURNAL OF CLINICAL PATHOLOGY, 1987, 40 (02) :157-162
[2]   MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES [J].
ALMOGUERA, C ;
SHIBATA, D ;
FORRESTER, K ;
MARTIN, J ;
ARNHEIM, N ;
PERUCHO, M .
CELL, 1988, 53 (04) :549-554
[3]   EXPRESSION OF P21RAS IN NORMAL AND MALIGNANT HUMAN-TISSUES - LACK OF ASSOCIATION WITH PROLIFERATION AND MALIGNANCY [J].
CHESA, PG ;
RETTIG, WJ ;
MELAMED, MR ;
OLD, LJ ;
NIMAN, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3234-3238
[4]  
CUBILLA AL, 1984, TUMORS EXOCRINE PANC, P5
[5]   ONCOGENES AND GASTROINTESTINAL CANCER [J].
FORGACS, I .
GUT, 1988, 29 (04) :417-421
[6]   RAS P21 EXPRESSION IN THE PROGRESSION OF BREAST-CANCER [J].
FROMOWITZ, FB ;
VIOLA, MV ;
CHAO, S ;
ORAVEZ, S ;
MISHRIKI, Y ;
FINKEL, G ;
GRIMSON, R ;
LUNDY, J .
HUMAN PATHOLOGY, 1987, 18 (12) :1268-1275
[7]   IMMUNOHISTOCHEMICAL DETECTION OF RAS ONCOGENE P21 PRODUCT IN BENIGN AND MALIGNANT MAMMARY TISSUE IN MAN [J].
GHOSH, AK ;
MOORE, M ;
HARRIS, M .
JOURNAL OF CLINICAL PATHOLOGY, 1986, 39 (04) :428-434
[8]   INTRINSIC GTPASE ACTIVITY DISTINGUISHES NORMAL AND ONCOGENIC RAS-P21 MOLECULES [J].
GIBBS, JB ;
SIGAL, IS ;
POE, M ;
SCOLNICK, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (18) :5704-5708
[9]   CYTOCHEMICAL DEMONSTRATION OF PEROXIDASE ACTIVITY WITH 3-AMINO-9-ETHYLCARBAZOLE [J].
GRAHAM, RC ;
LUNDHOLM, U ;
KARNOVSKY, MJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1965, 13 (02) :150-+
[10]  
ISHIKAWA J, 1988, ANTICANCER RES, V8, P915