MUC1 mucin mRNA expression in stage I lung adenocarcinoma and its association with early recurrence

被引:37
作者
Ohgami, A
Tsuda, T
Osaki, T
Mitsudomi, T
Morimoto, Y
Higashi, T
Yasumoto, K
机构
[1] Univ Occupat & Environm Hlth, Inst Ind Ecol Sci, Dept Environm Hlth Engn, Sch Med,Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[2] Univ Occupat & Environm Hlth, Sch Med, Dept Surg 2, Kitakyushu, Fukuoka 807, Japan
关键词
D O I
10.1016/S0003-4975(99)00041-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background MUC1 is a membrane-bound mucin with an extensively O-glycosylated core protein and is developmentally regulated and aberrantly expressed by carcinomas. A high level of MUC1 mucin expression and secretion is associated with high metastatic potential and a poor prognosis. We studied the expression of MUC1 messenger ribonucleic acid (mRNA) in stage I lung adenocarcinoma by reverse transcriptase-polymerase chain reaction and examined its correlation with early recurrence. Methods. The expression of MUC1 mRNA, in surgical specimens from 33 patients with stage I lung adenocarcinoma was determined by reverse transcriptase-polymerase chain reaction. The MUC1 and beta-actin sequences were subsequently coamplified to analyze the semiquantitative determination by polymerase chain reaction. The ratio of MUC1 to beta-actin product was used for further analysis. Results. An analysis of the disease-free survival (median follow-up, 33.4 months) revealed that a high expression of MUC1 was associated with early recurrence (p = 0.0191). Six of the 33 patients had recurrence within 2 years after operation. The recurrence sites suggested hematogenic metastasis. Conclusions. Our results indicate that MUC1 mRNA level may be useful as a marker of early recurrence in stage I lung adenocarcinoma. (Ann Thorac Surg 1999;67:810-4) (C) 1999 by The Society of Thoracic Surgeons.
引用
收藏
页码:810 / 814
页数:5
相关论文
共 30 条
[1]   Cancer-associated MUC1 mucin inhibits human T-cell proliferation, which is reversible by IL-2 [J].
Agrawal, B ;
Krantz, MJ ;
Reddish, MA ;
Longenecker, BM .
NATURE MEDICINE, 1998, 4 (01) :43-49
[2]   Significance of MUC1 and MUC2 mucin expression in colorectal cancer [J].
Ajioka, Y ;
Allison, LJ ;
Jass, JR .
JOURNAL OF CLINICAL PATHOLOGY, 1996, 49 (07) :560-564
[3]  
BOBEK LA, 1993, J BIOL CHEM, V268, P20563
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]  
GENDLER SJ, 1990, J BIOL CHEM, V265, P15286
[6]   EPITHELIAL MUCIN GENES [J].
GENDLER, SJ ;
SPICER, AP .
ANNUAL REVIEW OF PHYSIOLOGY, 1995, 57 :607-634
[7]   MOLECULAR-CLONING OF CDNAS DERIVED FROM A NOVEL HUMAN INTESTINAL MUCIN GENE [J].
GUM, JR ;
HICKS, JW ;
SWALLOW, DM ;
LAGACE, RL ;
BYRD, JC ;
LAMPORT, DTA ;
SIDDIKI, B ;
KIM, YS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (01) :407-415
[8]  
GUM JR, 1989, J BIOL CHEM, V264, P6480
[9]  
HO JJL, 1995, CANCER RES, V55, P3659
[10]   Vascular endothelial growth factor expression in non-small-cell lung cancer: Prognostic significance in squamous cell carcinoma [J].
Imoto, H ;
Osaki, T ;
Taga, S ;
Ohgami, A ;
Ichiyoshi, Y ;
Yasumoto, K .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1998, 115 (05) :1007-1014