Cheah P Y, Cao X, Eu K W, Seow-Choen F
Department of Colorectal Surgery, Singapore General Hospital, Republic of Singapore.
Br J Cancer. 1998 Apr;77(7):1164-8. doi: 10.1038/bjc.1998.193.
The NM23-H1 gene product has been recently identified as a potential metastasis suppressor. Studies on breast carcinomas have shown an inverse correlation between NM23-H1 status and stage of carcinogenesis and overall survival. However, in colorectal cancer, conflicting data have been reported. This study aimed to investigate whether NM23-H1 immunostaining is correlated with tumour stage, overall survival, disease recurrence, tumour differentiation, age and sex in colorectal carcinomas for the Singapore population using chi-square analysis. The staining was performed on 141 paraffin-embedded surgical specimens collected between 1991 and 1992 using a monoclonal anti-NM23-H1 antibody. Follow-up of patients was until time of death or for 5 years. There was a very significant inverse association between tumour staging and NM23-H1 status (P = 0.0004). However, NM23-H1 expression was not significantly correlated to overall 5-year survival, disease recurrence, tumour differentiation, age or sex. Thus, although NM23-H1 may be involved in suppressing metastasis, NM23-H1 immunohistochemistry has no prognostic value in colorectal cancer. This is the first report of a significant inverse association of NM23-H1 status with tumour staging in colorectal cancer which showed no correlation with overall survival or disease recurrence. Our result thus cautions against the practice of equating an inverse relation of genetic markers with tumour staging to survival or disease recurrence.
NM23-H1基因产物最近被确定为一种潜在的转移抑制因子。对乳腺癌的研究表明,NM23-H1状态与致癌作用阶段及总生存率之间呈负相关。然而,在结直肠癌方面,已报道的数据相互矛盾。本研究旨在使用卡方分析调查新加坡人群结直肠癌中NM23-H1免疫染色是否与肿瘤分期、总生存率、疾病复发、肿瘤分化、年龄和性别相关。使用单克隆抗NM23-H1抗体对1991年至1992年间收集的141份石蜡包埋手术标本进行染色。对患者的随访直至死亡或5年。肿瘤分期与NM23-H1状态之间存在非常显著的负相关(P = 0.0004)。然而,NM23-H1表达与5年总生存率、疾病复发、肿瘤分化、年龄或性别无显著相关性。因此,尽管NM23-H1可能参与抑制转移,但NM23-H1免疫组化在结直肠癌中没有预后价值。这是首次报道NM23-H1状态与结直肠癌肿瘤分期之间存在显著负相关,且与总生存率或疾病复发无相关性。因此,我们的结果提醒人们不要将遗传标记与肿瘤分期的负相关等同于生存率或疾病复发。