COX-2, inflammatory secreted PLA2, and cytoplasmic PLA2 protein expression in small bowel adenocarcinomas compared with colorectal adenocarcinomas

被引:43
作者
Wendum, D
Svrcek, M
Rigau, V
Boëlle, PY
Sebbagh, N
Parc, R
Masliah, J
Trugnan, G
Fléjou, JF
机构
[1] Hop St Antoine, Serv Anat Pathol, Dept Pathol, F-75571 Paris 12, France
[2] Hop St Antoine, Dept Digest Surg, F-75571 Paris, France
[3] Fac Med St Antoine, INSERM, U538, St Antoine, France
[4] Fac Med St Antoine, INSERM, U444, St Antoine, France
[5] Fdn Jean Dausset, CEPH, INSERM, U434, Paris, France
关键词
colorectal cancer; COX-2; cytoplasmic PLA2; immunohistochemistry; inflammatory secreted PLA2; small bowel cancer;
D O I
10.1097/01.MP.0000052101.58988.1F
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Cyclooxygenase-2 (COX-2), human synovial inflammatory secreted phospholipase A2 (sPLA2) and cytoplasmic phospholipase A2 (cPLA2) are involved in eicosanoid production and also seem to participate in colorectal tumorigenesis. As there are no data regarding these enzymes in human small bowel tumors, we wanted to determine whether they were involved in human small bowel tumorigenesis, and whether their expression was different in small bowel compared to colorectal adenocarcinomas, as suggested by animal studies. We studied their protein expression by immunohistochemistry in 25 small bowel adenocarcinomas and compared it to 48 colorectal adenocarcinomas. Seventy-six percent of the small bowel and 88% of the colorectal adenocarcinomas had a moderate or strong COX-2 expression. Sixty-eight percent of the small bowel and 67% of the colorectal adenocarcinomas had a moderate or strong sPLA2 expression. Forty-eight percent of the small bowel and 35% of the colorectal adenocarcinomas had a moderate or strong cPLA2 expression. In conclusion, the increased expression of COX-2, sPLA2, and sometimes cPLA2 in both small bowel and colorectal adenocarcinomas is in accordance with the likely eicosanoid involvement in tumor development. The same pattern of protein expression found in both types of adenocarcinoma contradicts experimental results in mice. Moreover, our results strengthen the similarities between these two types of human cancer.
引用
收藏
页码:130 / 136
页数:7
相关论文
共 43 条
[21]   THE SECRETORY PHOSPHOLIPASE-A2 GENE IS A CANDIDATE FOR THE MOM1 LOCUS, A MAJOR MODIFIER OF APC(MIN)-INDUCED INTESTINAL NEOPLASIA [J].
MACPHEE, M ;
CHEPENIK, KP ;
LIDDELL, RA ;
NELSON, KK ;
SIRACUSA, LD ;
BUCHBERG, AM .
CELL, 1995, 81 (06) :957-966
[22]   The functions of five distinct mammalian phospholipase A2S in regulating arachidonic acid release -: Type IIA and type V secretory phospholipase A2S are functionally redundant and act in concert with cytosolic phospholipase A2 [J].
Murakami, M ;
Shimbara, S ;
Kambe, T ;
Kuwata, H ;
Winstead, MV ;
Tischfield, JA ;
Kudo, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14411-14423
[23]  
Neugut AI, 1998, CANCER EPIDEM BIOMAR, V7, P243
[24]  
NEVALAINEN TJ, 1995, LAB INVEST, V72, P201
[25]  
Oshima M, 2001, CANCER RES, V61, P1733
[26]   Suppression of intestinal polyposis in Apc(Delta 716) knockout mice by inhibition of cyclooxygenase 2 (COX-2) [J].
Oshima, M ;
Dinchuk, JE ;
Kargman, SL ;
Oshima, H ;
Hancock, B ;
Kwong, E ;
Trzaskos, JM ;
Evans, JF ;
Taketo, MM .
CELL, 1996, 87 (05) :803-809
[27]   PATIENTS WITH ADENOMATOUS POLYPS AND CARCINOMAS HAVE INCREASED COLONIC MUCOSAL PROSTAGLANDIN E(2) [J].
PUGH, S ;
THOMAS, GAO .
GUT, 1994, 35 (05) :675-678
[28]   Genetic alterations in sporadic and Crohn's-associated adenocarcinomas of the small intestine [J].
Rashid, A ;
Hamilton, SR .
GASTROENTEROLOGY, 1997, 113 (01) :127-135
[29]  
Reddy BS, 2000, CANCER RES, V60, P293
[30]  
SANO H, 1995, CANCER RES, V55, P3785