Gastrointestinal nöroendokrin tümörlerde GLP-2 reseptör ekspresyonunun değerlendirilmesi

Süleyman Koç, Özgül Sağol, Mesut Akarsu
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Abstract

Evaluation of GLP-2 receptor expression in gastrointestinal neuroendocrine tumors Background and Aims: Neuroendocrine tumors arise from cells of the neuroendocrine system. These cells show both nerve and endocrine cell characteristics and can be found in many organs in the body. GLP-1 and GLP-2 are released from intestinal L cells in a 1:1 ratio following food intake. GLP-2 receptor recognizes GLP-2. GLP-2 receptor mRNA transcripts have been detected in the stomach, small and large intestine, brain, and lung. The proliferative effect of GLP-2 has been demonstrated in mice, rats, pigs, and humans by administering exogenous GLP-2. The objective is to evalaute the relation between gastroenteropancreatic neuroendocrine tumors and glukagon like peptid-2 and GLP-2 receptor. Materials and Methods: The patients, who were pathologically diagnosed with gastroenteropancreatic neuroendocrine tumor between 2006-2009 were included in the study. There were 47 patients (27 females, 20 males, avarage age: 54 ± 15.5) in the study. There were also 46 control group patients (25 females, 21 males, avarage age: 57.5 ± 14.8). Pathological tissue blocks prepared on poly-L-lysine microscope slides were stained by GLP-2 receptor antibody (1:100 - 1:200, 1 mg/ml) immunohistochemical stain. Results: GLP-2 receptor positivity of colon neuroendocrine tumor group was 30% (4/13) and colon control group was %100. GLP-2 receptor positivity of pancreas neuroendocrine tumor group was 25% (3/12) while it was 100% in pancreas control group. The comparison of colon neuroendocrine tumor and control group showed significant difference (p: 0.003). The comparison of pancreas neuroendocrine tumor and control group also showed statistically significant difference (p < 0.001). The comparison of gastric neuroendocrine tumor with the control yielded comparable results (p: 0.22). Conclusions: We concluded that GLP-2 receptor cannot be as useful as somatostatin receptors in diagnosis and treatment of these tumors. More studies are needed on this subject with different methods.
胃肠道神经内分泌肿瘤中GLP-2受体表达的研究背景与目的:神经内分泌肿瘤起源于神经内分泌系统的细胞。这些细胞具有神经细胞和内分泌细胞的特点,存在于人体的许多器官中。GLP-1和GLP-2在食物摄入后以1:1的比例从肠L细胞释放。GLP-2受体识别GLP-2。GLP-2受体mRNA转录本已在胃、小肠和大肠、脑和肺中检测到。通过施用外源性GLP-2, GLP-2在小鼠、大鼠、猪和人类中已经证明了其增殖作用。目的是探讨胰高血糖素样肽-2和胰高血糖素-2受体与胃肠胰神经内分泌肿瘤的关系。材料与方法:选取2006-2009年病理诊断为胃肠胰神经内分泌肿瘤的患者为研究对象。共47例患者,其中女性27例,男性20例,平均年龄54±15.5岁。对照组患者46例,其中女性25例,男性21例,平均年龄57.5±14.8岁。采用GLP-2受体抗体(1:100 ~ 1:200,1 mg/ml)免疫组化染色,在聚l -赖氨酸显微镜载玻片上制备病理组织块。结果:结肠神经内分泌肿瘤组GLP-2受体阳性30%(4/13),结肠对照组GLP-2受体阳性%100。胰腺神经内分泌肿瘤组GLP-2受体阳性25%(3/12),胰腺对照组GLP-2受体阳性100%。结肠神经内分泌肿瘤与对照组比较,差异有统计学意义(p: 0.003)。胰腺神经内分泌肿瘤与对照组比较,差异有统计学意义(p < 0.001)。胃神经内分泌肿瘤组与对照组的比较结果相当(p: 0.22)。结论:我们认为GLP-2受体在这些肿瘤的诊断和治疗中不如生长抑素受体有用。需要用不同的方法对这个问题进行更多的研究。
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