HIGH-LEVEL OF NM23-H1 GENE-EXPRESSION IS ASSOCIATED WITH LOCAL COLORECTAL-CANCER PROGRESSION NOT WITH METASTASES

被引:43
作者
ZENG, ZS
HSU, S
ZHANG, ZF
COHEN, AM
ENKER, WE
TURNBULL, AA
GUILLEM, JG
机构
[1] MEM SLOAN KETTERING CANC CTR, DEPT SURG, COLORECTAL SERV, NEW YORK, NY 10021 USA
[2] MEM SLOAN KETTERING CANC CTR, DEPT SURG, GASTR & MIXED TUMOUR SERV, NEW YORK, NY 10021 USA
[3] MEM SLOAN KETTERING CANC CTR, DEPT MED, GASTROENTEROL SERV, NEW YORK, NY 10021 USA
[4] MEM SLOAN KETTERING CANC CTR, DEPT STAT, EPIDEMIOL SERV, NEW YORK, NY 10021 USA
关键词
D O I
10.1038/bjc.1994.442
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study aimed to determine the expression of Nm23-H1 in colorectal cancer and liver metastases and to correlate Nm23-H1 expression with clinicopathological variables. Specimens from 59 primary colorectal cancers and five liver metastases were studied using Northern blot hybridisation. The mean +/- s.e. of tumour/normal (T/N) ratio of Nm23-H1 RNA expression was 4.3 +/- 0.4 (P<0.001) and 5.1 +/- 0.90 (P<0.01) for colorectal cancer and liver metasases respectively. No significant relationship was observed between the level of Nm23-H1 RNA and the patient's age, sex, tumour location, differentiation, presence of lymph node involvement or distant metastases. Nm23-H1 RNA level was 2.6 +/- 0.5 for tumour size less than 3.0 cm and 4.6 +/- 0.5 for those greater than or equal to 3.0 cm (P = 0.05). There appeared to be a trend between increasing relative Nm23-H1 RNA and bowel wall invasion, irrespective of metastatic status (T1 = 1.9 +/- 0.3, T2 = 4.1 +/- 0.6, T3 = 4.1 +/- 0.5 and T4 = 6.4 +/- 1.6). This difference was statistically significant when T1 was compared against greater than or equal to T2 lesions (P = 0.01). Western blot analysis reveals two Nm23H-1 bands (17.0 kDa and 18.5 kDa). In 16 colorectal patients, the T/N fold-increase in protein expression was 2.66 +/- 0.46 (P<0.001) and 2.40 +/- 0.32 (P<0.001) for the 17.0 and 18.5 kDa band respectively. Both Nm23-H1 RNA and protein levels in primary colorectal cancers do not appear to correlate with synchronous regional or distant metastases. Since Nm23-H1 RNA expression is associated with increasing tumour size and tumour local invasion, Nm23-H1 RNA expression may be associated with local disease progression.
引用
收藏
页码:1025 / 1030
页数:6
相关论文
共 40 条
[1]   REDUCED EXPRESSION OF NM23 PROTEIN IS ASSOCIATED WITH ADVANCED TUMOR STAGE AND DISTANT METASTASES IN HUMAN COLORECTAL CARCINOMAS [J].
AYHAN, A ;
YASUI, W ;
YOKOZAKI, H ;
KITADAI, Y ;
TAHARA, E .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1993, 63 (04) :213-218
[2]  
BACKER JM, 1993, ONCOGENE, V8, P497
[3]  
BARNES R, 1991, AM J PATHOL, V139, P245
[4]  
BEVILACQUA G, 1989, CANCER RES, V49, P5185
[5]   ASSOCIATION OF NM23-H1 ALLELIC DELETIONS WITH DISTANT METASTASES IN COLORECTAL-CARCINOMA [J].
COHN, KH ;
WANG, FS ;
DESOTOLAPAIX, F ;
SOLOMON, WB ;
PATTERSON, LG ;
ARNOLD, MR ;
WEIMAR, J ;
FELDMAN, JG ;
LEVY, AT ;
LEONE, A ;
STEEG, PS .
LANCET, 1991, 338 (8769) :722-724
[6]   HIGH-LEVELS OF NM23-H1 AND NM23-H2 MESSENGER-RNA IN HUMAN SQUAMOUS-CELL LUNG-CARCINOMA ARE ASSOCIATED WITH POOR DIFFERENTIATION AND ADVANCED TUMOR STAGES [J].
ENGEL, M ;
THEISINGER, B ;
SEIB, T ;
SEITZ, G ;
HUWER, H ;
ZANG, KD ;
WELTER, C ;
DOOLEY, S .
INTERNATIONAL JOURNAL OF CANCER, 1993, 55 (03) :375-379
[7]   DEREGULATION OF C-MYC GENE-EXPRESSION IN HUMAN-COLON CARCINOMA IS NOT ACCOMPANIED BY AMPLIFICATION OR REARRANGEMENT OF THE GENE [J].
ERISMAN, MD ;
ROTHBERG, PG ;
DIEHL, RE ;
MORSE, CC ;
SPANDORFER, JM ;
ASTRIN, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (08) :1969-1976
[8]   EXPRESSION OF A POTENTIAL METASTASIS SUPPRESSOR GENE (NM23) IN THYROID NEOPLASMS [J].
FARLEY, DR ;
EBERHARDT, NL ;
GRANT, CS ;
SCHAID, DJ ;
VANHEERDEN, JA ;
HAY, ID ;
KHOSLA, S .
WORLD JOURNAL OF SURGERY, 1993, 17 (05) :615-621
[9]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[10]  
FLORENES VA, 1992, CANCER RES, V52, P6088