Ayed Dorra Ben, Khabir Abdelmajid, Abid Mohamed, Bayrouti Mohamed Issam, Gargouri Ali, Sellami-Boudawara Tahia, Mokdad-Gargouri Raja
Center of Biotechnology of Sfax, University of Sfax, BP K 3018, Sfax, Tunisia; Department of Anatomy-Pathology, Habib Bourguiba Hospital, Sfax, Tunisia.
Department of Anatomy-Pathology, Habib Bourguiba Hospital, Sfax, Tunisia.
Acta Histochem. 2014 Oct;116(8):1244-50. doi: 10.1016/j.acthis.2014.07.008. Epub 2014 Aug 3.
Gastric carcinoma (GC) is a highly aggressive malignancy with poor prognosis. It is widely accepted that malignancy results from abnormal cell growth due to dysregulation of the balance between cell proliferation and apoptosis. Our study aimed to investigate the clinicopathological and prognostic significance of p53, Ki-67, and Bcl-2 in Tunisian GC patients by immunohistochemistry. It was observed that the older patients showed p53 overexpression compared with the younger patients (p<0.05). There was higher p53 expression in the intestinal-type compared with the diffuse-type (p<0.05), and in well/moderate differentiated than in poor differentiated tumors. The expression of Ki-67 was positively associated with tumor size and venous invasion (p<0.05). Bcl2 expression occurred in male patients and correlated with depth of invasion (p=0.02). A Kaplan-Meier analysis indicated an inverse correlation between p53 and Ki-67 expression and the overall survival. Multivariate analysis revealed that the tumor site, Ki-67 and p53 expression were independent prognostic factors for gastric carcinomas (p<0.05). Finally, combined expression of p53, Ki-67 and Bcl-2 showed that the group of patients with tumors p53+/Ki-67+/Bcl2- had aggressive behavior and poor prognosis (p log rank=0.000). In summary, our data indicated that the expression of p53, Ki-67, and Bcl-2 may provide useful information for identifying patients with aggressive behavior and poor prognosis of GC.
胃癌(GC)是一种侵袭性很强的恶性肿瘤,预后较差。人们普遍认为,恶性肿瘤是由于细胞增殖和凋亡之间的平衡失调导致细胞生长异常所致。我们的研究旨在通过免疫组织化学研究p53、Ki-67和Bcl-2在突尼斯胃癌患者中的临床病理及预后意义。观察发现,老年患者与年轻患者相比,p53表达上调(p<0.05)。肠型胃癌的p53表达高于弥漫型(p<0.05),高/中分化肿瘤的p53表达高于低分化肿瘤。Ki-67的表达与肿瘤大小和静脉侵犯呈正相关(p<0.05)。Bcl2表达见于男性患者,且与浸润深度相关(p=0.02)。Kaplan-Meier分析表明,p53和Ki-67表达与总生存期呈负相关。多因素分析显示肿瘤部位、Ki-67和p53表达是胃癌的独立预后因素(p<0.05)。最后,p53、Ki-67和Bcl-2的联合表达显示,肿瘤为p53+/Ki-67+/Bcl2-的患者组具有侵袭性行为且预后较差(p对数秩检验=0.000)。总之,我们的数据表明,p53、Ki-67和Bcl-2的表达可为识别具有侵袭性行为和预后较差的胃癌患者提供有用信息。