Apoptosis inhibiting factor Bcl-xL might be the crucial member of the Bcl-2 gene family in colorectal cancer

被引:79
作者
Maurer, CA
Friess, H
Bühler, SS
Wahl, BR
Graber, H
Zimmermann, A
Büchler, MW [1 ]
机构
[1] Univ Bern, Inselspital, Clin Visceral & Transplantat Surg, CH-3010 Bern, Switzerland
[2] Univ Bern, Inst Pathol, Bern, Switzerland
关键词
apoptosis; colorectal neoplasms; Bcl-2; Bcl-x(L); Bax; Bak; Northern blots; immunohistochemistry;
D O I
10.1023/A:1026695025990
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Since the role of the Bcl-2 gene family has been only poorly investigated in colorectal cancer, we have examined the expression of the apoptosis blockers Bcl-x(L) and Bcl-2, as well as the proapoptotic factors Bax and Bak. Northern blot analysis and immunohistochemistry were performed on normal and cancerous colonic tissue from 12 patients. In colorectal cancer, Bcl-x(L) immunoreaction was stronger than in normal controls, and 83% of the cancers had increased Bcl-x(L) mRNA expression. The median densitometric Bcl-x(L) values were 3.4-fold higher in carcinomas (P < 0.005). In contrast to the normal colon, colorectal carcinomas often lack any Bcl-2 immunostaining, and Eel-2 mRNA was not detectable by Northern blots either. Bax was not obviously altered in colorectal cancer, either at the protein level or at the mRNA level compared to the normal control colon. Bak mRNA expression exhibited a wide variation in carcinomas, but was somewhat decreased in comparison to the controls. Of these members of the Eel-2 gene family, Bcl-x(L) seems to play a major role in colorectal tumori genesis and disease progression. An agonistic effect might have caused the tendency for reduced Bak expression. The Bcl-2/Bax regulation system of cell homeostasis seems to be of lesser importance.
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收藏
页码:2641 / 2648
页数:8
相关论文
共 31 条
[1]  
Baretton GB, 1996, CANCER, V77, P255, DOI 10.1002/(SICI)1097-0142(19960115)77:2<255::AID-CNCR6>3.0.CO
[2]  
2-L
[3]  
BEDI A, 1995, CANCER RES, V55, P1811
[4]  
Boise L H, 1995, Curr Top Microbiol Immunol, V200, P107
[5]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[6]   Bax-independent inhibition of apoptosis by Bcl-x(L) [J].
Cheng, EHY ;
Levine, B ;
Boise, LH ;
Thompson, CB ;
Hardwick, JM .
NATURE, 1996, 379 (6565) :554-556
[7]   INDUCTION OF APOPTOSIS BY THE BCL-2 HOMOLOG BAK [J].
CHITTENDEN, T ;
HARRINGTON, EA ;
OCONNOR, R ;
FLEMINGTON, C ;
LUTZ, RJ ;
EVAN, GI ;
GUILD, BC .
NATURE, 1995, 374 (6524) :733-736
[8]  
DESCHNER EE, 1990, KINETICS NORMAL PREN, P41
[9]   IDENTIFICATION OF IMMUNOSUPPRESSANT-INDUCED APOPTOSIS IN A MURINE B-CELL LINE AND ITS PREVENTION BY BCL-X BUT NOT BCL-2 [J].
GOTTSCHALK, AR ;
BOISE, LH ;
THOMPSON, CB ;
QUINTANS, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7350-7354
[10]  
Kaklamanis L, 1996, J PATHOL, V179, P10