Shareef Mohamed Moustafa, Radi Dina Mohammed Adel, Eid Asmaa Mustafa Mohammed
Department of Pathology, Tanta University, Egypt.
Department of Pathology, Tanta University, Egypt.
Arab J Gastroenterol. 2015 Sep-Dec;16(3-4):105-12. doi: 10.1016/j.ajg.2015.09.008. Epub 2015 Oct 31.
Gastric cancer is the second most common cause of cancer-related death worldwide. Claudins are a family of tight junction proteins that are biologically relevant in many cancer progression steps. This study aimed to investigate the expression of the intestinal claudin (claudin 4) in gastric carcinoma and to evaluate its relation to the different clinicopathologic prognostic parameters, especially lymphangiogenesis (production of new lymphatic vessels, measured by lymphovascular density (LVD)) and lymphovascular invasion (LVI).
Fifty-five gastric carcinoma specimens were immunohistochemically stained for claudin 4 and D2-40 (for detection of lymphatic vessel endothelium).
High expression of claudin 4 was detected in 26 of 55 (47.3%) cases. Low expression of claudin 4 was related to poorly differentiated type (p=0.001), non-intestinal (diffuse) type (p=0.001), deeper tumour invasion (p<0.001), lymph node metastasis (p=0.001), and higher stage (p=0.001). In addition, higher LVD was related to poorly differentiated types (p=0.001), non-intestinal type (p=0.001), lymph node metastasis (p=0.015), and higher tumour, node, metastasis (TNM) stage (p=0.001). LVI was related to lymph node metastasis (p=0.025), higher TNM stage (p=0.001), and LVD (p=0.001). Claudin 4 significantly correlated with both LVD (p=0.009) and LVI (p=0.009).
High expression of claudin 4 was associated with the more differentiated intestinal-type gastric carcinoma and lost in poorly differentiated diffuse type. So, claudin 4 may be used as one of the differentiating markers between the two major types of gastric carcinoma (intestinal vs. diffuse). LVD and LVI were related to higher incidence of lymph node metastasis and therefore could be used as predictive markers for lymph node metastasis in limited specimens during early gastric carcinoma to determine the need for more invasive surgery. Low expression of claudin 4 was related to lymphangiogenesis. This may shed light on the relation of tight junction protein expression and lymphangiogenesis.
胃癌是全球癌症相关死亡的第二大常见原因。紧密连接蛋白是一类紧密连接蛋白家族,在许多癌症进展步骤中具有生物学相关性。本研究旨在调查肠型紧密连接蛋白(紧密连接蛋白4)在胃癌中的表达,并评估其与不同临床病理预后参数的关系,尤其是淋巴管生成(通过淋巴管密度(LVD)测量的新淋巴管生成)和淋巴管侵犯(LVI)。
对55例胃癌标本进行紧密连接蛋白4和D2-40(用于检测淋巴管内皮)的免疫组织化学染色。
55例中有26例(47.3%)检测到紧密连接蛋白4高表达。紧密连接蛋白4低表达与低分化型(p=0.001)、非肠型(弥漫型)(p=0.001)、肿瘤浸润更深(p<0.001)、淋巴结转移(p=0.001)及更高分期(p=0.001)相关。此外,更高的LVD与低分化型(p=0.001)、非肠型(p=0.001)、淋巴结转移(p=0.015)及更高的肿瘤、淋巴结、转移(TNM)分期(p=0.001)相关。LVI与淋巴结转移(p=0.025)、更高的TNM分期(p=0.001)及LVD(p=0.001)相关。紧密连接蛋白4与LVD(p=0.009)和LVI(p=0.009)均显著相关。
紧密连接蛋白4高表达与分化程度更高的肠型胃癌相关,而在低分化弥漫型中缺失。因此,紧密连接蛋白4可作为两种主要类型胃癌(肠型与弥漫型)之间的鉴别标志物之一。LVD和LVI与淋巴结转移的更高发生率相关,因此可在早期胃癌有限标本中用作淋巴结转移的预测标志物,以确定是否需要更具侵入性的手术。紧密连接蛋白4低表达与淋巴管生成相关。这可能有助于揭示紧密连接蛋白表达与淋巴管生成之间的关系。