Wang Ying, Li Zhao-Fa, He Jin, Li Yi-Lei, Zhu Gui-Bin, Zhang Li-Hong, Li Yu-Lin
The Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun, China.
Int J Colorectal Dis. 2007 Oct;22(10):1179-84. doi: 10.1007/s00384-007-0303-1. Epub 2007 Apr 18.
Human phosphatases of regenerating liver (PRLs) can induce cell growth, differentiation, and malignant transformation. In this study, we used specific polyclonal antibodies against PRLs to investigate their expression in colonic adenocarcinomas and its correlation with patient gender, age, tumor differentiation, localization, invasion, and metastasis.
The polyclonal antibodies against PRL-1, PRL-2, and PRL-3 were produced and purified. The expression of PRLs in human colorectal carcinoma cell lines (SW480 and SW620) was examined by Western blotting. We also examined their expression in normal and pathologic tissues from the human colon. The tissues included 49 primary colonic adenocarcinomas, 14 cases with lymph node metastases, 15 colonic adenomas, and 12 normal colon samples. Hematoxylin and eosin staining, immunohistochemistry, and semiquantitative morphological analysis were used to evaluate the sections.
PRLs were widely expressed in SW480 and SW620. PRL-1, PRL-2, and PRL-3 were expressed, respectively, in 16, 10, and 16% of primary colonic adenocarcinomas. In contrast, PRLs were strongly expressed in all lymph node metastases. There were no significant correlations between the expression of PRLs and patient gender, age, tumor differentiation, depth of invasion, or localization of tumor within the different sections of the colon. PRLs were not expressed in normal colon tissues or in colonic adenomas. PRLs were mainly expressed in the cytoplasm and at the cytoplasmic membranes of the colonic adenocarcinoma cells as well as in the endothelial cells and the surrounding smooth muscle cells of larger vessels in the lymph node metastases.
Colonic adenocarcinoma cells have the ability to produce PRLs, which may relate to the lymph node metastasis of colonic adenocarcinoma.
再生肝脏磷酸酶(PRLs)可诱导细胞生长、分化及恶性转化。在本研究中,我们使用针对PRLs的特异性多克隆抗体,研究其在结肠腺癌中的表达及其与患者性别、年龄、肿瘤分化、定位、侵袭和转移的相关性。
制备并纯化针对PRL-1、PRL-2和PRL-3的多克隆抗体。通过蛋白质免疫印迹法检测PRLs在人结肠癌细胞系(SW480和SW620)中的表达。我们还检测了它们在人结肠正常和病理组织中的表达。组织包括49例原发性结肠腺癌、14例有淋巴结转移的病例、15例结肠腺瘤和12例正常结肠样本。采用苏木精-伊红染色、免疫组织化学和半定量形态学分析对切片进行评估。
PRLs在SW480和SW620中广泛表达。PRL-1、PRL-2和PRL-3分别在16%、10%和16%的原发性结肠腺癌中表达。相比之下,PRLs在所有淋巴结转移中均强烈表达。PRLs的表达与患者性别、年龄、肿瘤分化、侵袭深度或肿瘤在结肠不同节段的定位之间无显著相关性。PRLs在正常结肠组织或结肠腺瘤中不表达。PRLs主要表达于结肠腺癌细胞的细胞质和细胞膜以及淋巴结转移灶中较大血管的内皮细胞和周围平滑肌细胞。
结肠腺癌细胞具有产生PRLs的能力,这可能与结肠腺癌的淋巴结转移有关。