Connexin 26 is abnormally expressed in bladder cancer

被引:30
作者
Gee, J [1 ]
Tanaka, M [1 ]
Grossman, HB [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
关键词
bladder; bladder neoplasms; connexins; gap junctions;
D O I
10.1097/01.ju.0000041954.91331.df
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Connexin 26 is the major gap junction protein in urothelial and mammary epithelial cells, and a putative tumor suppressor gene. We evaluated connexin 26 expression in normal urothelium and in bladder cancer. Materials and Methods: A total of 40 formalin fixed, paraffin embedded bladder tumors and 5 normal urothelial specimens were analyzed by immunohistochemistry. Two observers visually scored connexin 26 expression in these specimens. Results: Normal urothelium expressed connexin 26 in a punctate staining pattern with limited expression in the basal layer. Decreased connexin 26 expression was observed in 28 of 40 tumors (70%). Connexin 26 was diffusely expressed in 5 of 18 low grade, noninvasive tumors (28%), whereas loss of expression was observed in heterogeneous (30% to 70% positive staining) or extensive (less than 30% positive staining) fashion in 8 (44%) and 5 (28%), respectively. Seven of 22 high grade or invasive tumors (32%) showed diffuse connexin 26 expression, whereas expression was decreased in a heterogeneous or extensive pattern in 9 (41%) and 6 (27%), respectively. Intracytoplasmic localization of connexin 26 was also observed. Conclusions: Expression of connexin 26 is altered in bladder cancer. These aberrant patterns of connexin 26 expression may contribute to the malignant phenotype of this disease.
引用
收藏
页码:1135 / 1137
页数:3
相关论文
共 19 条
[1]   Connections with connexins: The molecular basis of direct intercellular signaling [J].
Bruzzone, R ;
White, TW ;
Paul, DL .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 238 (01) :1-27
[2]   Disruption of gap junctional intercellular communication by lindane is associated with aberrant localization of connexin43 and zonula occludens-1 in 42GPA9 Sertoli cells [J].
Defamie, N ;
Mograbi, B ;
Roger, C ;
Cronier, L ;
Malassine, A ;
Brucker-Davies, F ;
Fenichel, P ;
Segretain, D ;
Pointis, G .
CARCINOGENESIS, 2001, 22 (09) :1537-1542
[3]  
Erbersdobler A, 1998, ONCOL RES, V10, P415
[4]  
GROSSMAN HB, 1994, CANCER RES, V54, P3062
[5]  
Hirschi KK, 1996, CELL GROWTH DIFFER, V7, P861
[6]  
KRUTOVSKIKH V, 1994, INT J CANCER, V56, P87
[7]   TRANSCRIPTIONAL DOWN-REGULATION OF GAP-JUNCTION PROTEINS BLOCKS JUNCTIONAL COMMUNICATION IN HUMAN MAMMARY-TUMOR CELL-LINES [J].
LEE, SW ;
TOMASETTO, C ;
PAUL, D ;
KEYOMARSI, K ;
SAGER, R .
JOURNAL OF CELL BIOLOGY, 1992, 118 (05) :1213-1221
[8]  
Mehta P, 1999, DEV GENET, V24, P91, DOI 10.1002/(SICI)1520-6408(1999)24:1/2<91::AID-DVG10>3.0.CO
[9]  
2-#
[10]  
MESNIL M, 1995, CANCER RES, V55, P629