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Her2/neu Protein Expression and Oncogene Amplification in Gastric Carcinoma with Clinico-Pathological Correlation in Egyptian Patients

机译:埃及患者中Her2 / neu蛋白表达与胃癌临床病理相关性的癌基因扩增

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摘要

AIM: Amplification of the Her2/neu gene and overexpression of the Her2/neu protein in gastric carcinoma (GC) is a golden criterion for target therapy with trastuzumab (Herceptin). We aim to evaluate the immunohistochemical protein expression and amplification of the oncogene Her2/neu by FISH technique in the epithelial gastric carcinoma and to compare their association with different clinicopathologic parameters aiming at identifying positive cases that may benefit from targeted therapy.MATERIALS AND METHODS: This study was done on eighty-five tumour tissue samples from patients with GC as well as thirty non-malignant lesions (Gastritis, intestinal metaplasia, adenoma with low-grade dysplasia, adenoma with high-grade dysplasia). All were immunohistochemically stained with Her2/neu antibody.RESULTS: All equivocal and some selected GC cases were submitted for FISH technique to detect Her2/neu gene amplification. By immunohistochemistry twenty-three cases (27%) were defined as positive for Her2/neu gene amplification and/or protein overexpression. The levels of Her2/neu positive (3+), Her2/neu equivocal (2+) and Her2/neu negative (1+/0) were measurable in 14.2%, 32.9% and 52.9% of the samples, respectively. FISH showed that Her2/neu gene was amplified in 22 cases, 10 Her2/neu positive (3+), 11 (39.3%) Her2/neu equivocal (2+) and 1 Her2/neu negative (1+) cases with IHC staining those who can benefit from anti Her2/neu target therapy. Her2/neu was overexpressed positivity (3+) more in intestinal type and mixed carcinoma, and moderately differentiated tumours. None of gastritis, intestinal metaplasia or adenoma with low-grade dysplasia cases showed positivity for Her2/neu (3+). The Her2/neu positivity (3+) was associated with both adenocarcinoma cases and high-grade dysplasia (P = 0.002).CONCLUSIONS: The results highlight the necessity of FISH test for further categorization when gastric cancer cases are equivocal (2+) by IHC to determine eligibility for the targeted therapy. Stepwise increase in the expression of Her2/neu was seen in low-grade dysplasia, high-grade dysplasia and carcinoma cases implying its role in cancer evolution. Overexpression of Her 2/neu in GC patients can be promising in selecting those who can get benefit from anti-Her2/neu target therapy.
机译:目的:胃癌(GC)中Her2 / neu基因的扩增和Her2 / neu蛋白的过度表达是曲妥珠单抗(赫赛汀)靶向治疗的黄金标准。我们旨在通过FISH技术评估癌基因Her2 / neu在上皮性胃癌中的免疫组织化学蛋白表达和扩增,并比较它们与不同临床病理学参数的关联,旨在确定可能受益于靶向治疗的阳性病例。对来自GC患者以及三十五个非恶性病变(胃炎,肠上皮化生,低度不典型增生的腺瘤,高度不典型增生的腺瘤)的八十五份肿瘤组织样本进行了研究。结果:所有Her2 / neu抗体均经过免疫组织化学染色。结果:所有模棱两可的病例和部分GC病例均经FISH技术检测Her2 / neu基因扩增。通过免疫组织化学,将23例(27%)定义为Her2 / neu基因扩增和/或蛋白过表达阳性。分别测量了14.2%,32.9%和52.9%的样本中Her2 / neu阳性(3 +),Her2 / neu模棱两可(2+)和Her2 / neu阴性(1 + / 0)的水平。 FISH结果显示,通过IHC染色,在22例病例中扩增了Her2 / neu基因,其中10例Her2 / neu阳性(3 +),11例(39.3%)Her2 / neu模棱两可(2+)和1例Her2 / neu阴性(1+)那些可以从抗Her2 / neu靶向治疗中受益的人。 Her2 / neu在肠型和混合癌以及中度分化的肿瘤中高表达(3+)阳性。轻度不典型增生的胃炎,肠上皮化生或腺瘤均未显示出Her2 / neu(3+)阳性。 Her2 / neu阳性(3+)与腺癌病例和高度不典型增生有关(P = 0.002)。结论:结果表明,当胃癌病例不明确(2+)时,FISH检测有必要进一步分类。 IHC确定目标疗法的资格。在低度异型增生,高度异型增生和癌病例中观察到Her2 / neu表达的逐步增加,提示其在癌症演变中的作用。在选择GC / Her2 / neu靶向治疗受益者时,GC患者中Her 2 / neu的过表达可能很有希望。

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