Cho Yong-Gu, Kim Chang-Jae, Nam Suk-Woo, Yoon Shin-Hee, Lee Sug-Hyung, Yoo Nam-Jin, Lee Jung-Young, Park Won-Sang
Department of Pathology, College of Medicine, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul 137-701, South Korea.
World J Gastroenterol. 2005 Aug 21;11(31):4852-6. doi: 10.3748/wjg.v11.i31.4852.
To investigate whether S100A4 played an important role in the development or progression of colorectal cancer.
A total of 124 colorectal adenocarcinoma tissue specimens were analyzed by immunohistochemistry for the expression of S100A4 protein and subsequently investigated for the gene mutations in the coding region of S100A4 gene. The specimens were collected over a 3-year period in the laboratories at our large teaching hospital in Seoul, Republic of Korea.
Normal colonic epithelium either failed to express or showed focal weak expression of S100A4. Moderate to strong cytoplasmic expression of S100A4 was seen in 69 (55.6%) of the 124 colorectal carcinoma tissue specimens. S100A4 expression was detected in 43 (69.4%) of 62 specimens with lymph node metastasis. Statistically, overexpression of S100A4 was significantly associated with Dukes' stage and lymph node metastasis. Nuclear staining was also observed in 24 (19.4%) of 124 samples and closely associated with Dukes' stage. However, there was no significant correlation between overexpression of S100A4 and other investigated clinico-pathologic parameters, including tumor localization, tumor size, and survival period. In mutational analysis, no gene mutation was found in the analyzed genomic area of colorectal cancer.
Overexpression of S100A4 may be closely related with the aggressiveness of colorectal carcinoma.
研究S100A4在结直肠癌的发生发展过程中是否发挥重要作用。
采用免疫组织化学方法分析124例结直肠癌组织标本中S100A4蛋白的表达情况,并对S100A4基因编码区进行基因突变检测。这些标本是在韩国首尔一家大型教学医院的实验室中,历时3年收集的。
正常结肠上皮细胞要么不表达S100A4,要么仅表现为局灶性弱表达。在124例结直肠癌组织标本中,69例(55.6%)可见S100A4中度至强细胞质表达。在62例有淋巴结转移的标本中,43例(69.4%)检测到S100A4表达。统计学分析显示,S100A4的过表达与Dukes分期和淋巴结转移显著相关。在124例样本中,24例(19.4%)还观察到细胞核染色,且与Dukes分期密切相关。然而,S100A4的过表达与其他研究的临床病理参数,包括肿瘤定位、肿瘤大小和生存期之间无显著相关性。在突变分析中,未在结直肠癌分析的基因组区域发现基因突变。
S100A4的过表达可能与结直肠癌的侵袭性密切相关。