Hadi Ahmed Abdel, Hindawi Ali El, Hareedy Amal, Khalil Heba, Ashiry Ranya Al, Elia Shady, Sadek Ahmed, Magdy Mona, Atta Rafatt, Anas Amgad, Bakr Hisham, Hammam Olfat
Theodor Bilharz Research Institute, Imbaba, Giza, Cairo, Egypt.
Faculty of Medicine Cairo University, Cairo, Egypt.
Open Access Maced J Med Sci. 2016 Dec 15;4(4):535-542. doi: 10.3889/oamjms.2016.104. Epub 2016 Sep 11.
Amplification of the Her2/neu gene and overexpression of the 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.
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.
All equivocal and some selected GC cases were submitted for FISH technique to detect gene amplification. By immunohistochemistry twenty-three cases (27%) were defined as positive for 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 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. 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).
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.
人表皮生长因子受体2(Her2/neu)基因扩增及蛋白在胃癌(GC)中的过表达是曲妥珠单抗(赫赛汀)靶向治疗的黄金标准。我们旨在通过荧光原位杂交(FISH)技术评估原发性胃癌中癌基因Her2/neu的免疫组化蛋白表达及扩增情况,并比较其与不同临床病理参数的相关性,以确定可能从靶向治疗中获益的阳性病例。
本研究对85例GC患者的肿瘤组织样本以及30例非恶性病变(胃炎、肠化生、低级别不典型增生腺瘤、高级别不典型增生腺瘤)进行了研究。所有样本均用Her2/neu抗体进行免疫组化染色。
所有可疑及部分选定的GC病例均接受FISH技术检测基因扩增。通过免疫组化,23例(27%)被定义为基因扩增和/或蛋白过表达阳性。Her2/neu阳性(3+)、Her2/neu可疑(2+)和Her2/neu阴性(1+/0)的样本比例分别为14.2%、32.9%和52.9%。FISH显示22例基因扩增,其中10例Her2/neu阳性(3+),11例(39.3%)Her2/neu可疑(2+),1例Her2/neu阴性(1+),免疫组化染色显示这些病例可从抗Her2/neu靶向治疗中获益。Her2/neu过表达阳性(3+)在肠型和混合型癌以及中分化肿瘤中更为常见。胃炎、肠化生或低级别不典型增生腺瘤病例中均未发现Her2/neu(3+)阳性。Her2/neu阳性(3+)与腺癌病例和高级别不典型增生均相关(P = 0.002)。
结果强调了在免疫组化结果为可疑(2+)的胃癌病例中,进行FISH检测以进一步分类从而确定靶向治疗适用性的必要性。在低级别不典型增生、高级别不典型增生和癌病例中,Her2/neu表达呈逐步增加,这暗示了其在癌症进展中的作用。GC患者中Her2/neu的过表达对于选择可能从抗Her2/neu靶向治疗中获益的患者具有指导意义。