EGFR在三阴性乳腺癌中的表达及基因拷贝数

Berrak Gumuskaya , Murat Alper , Sema Hucumenoglu , Kadri Altundag , Aysegul Uner , Gulnur Guler
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引用次数: 68

摘要

大多数基底样乳腺癌是雌激素受体阴性,孕激素受体阴性,cerb-B2/HER-2/neu阴性,即所谓的三阴性乳腺癌,具有高表达的表皮生长因子受体(EGFR),这使得EGFR成为治疗的目标。本研究采用免疫组化(IHC)方法检测了2个不同克隆(EGFR. 31g7和EGFR.25)在62例三阴性乳腺癌中的表达,并采用基因座特异性标识EGFR/CEP 7双探针荧光原位杂交(FISH)方法检测了基因拷贝数。任何完全或不完全的膜和/或细胞质表达都被认为是IHC阳性。出现基因扩增(≥10%的细胞中EGFR基因与7号染色体的比例为每个细胞≥2或15个拷贝)和高多体(≥40%的细胞中≥4个拷贝)的病例被认为是FISH阳性。62例中有38例(61.4%)检测到EGFR.31G7阳性,其中细胞质染色12例(19.4%),不完全膜性染色14例(22.6%),完全膜性染色12例(19.4%)。49例egfr .25阳性38例(77.6%)中,7例(14.3%)为细胞质染色,10例(20.4%)为不完全膜性染色,21例(42.9%)为完全膜性染色。62例fish阳性病例中发现10例(16.1%);62例中1例(1.6%)扩增,其余为高多体。两种EGFR克隆均显示fish阳性病例IHC阳性(P = 0.01)。扩增的病例在两个克隆中都显示出强烈的完全膜性染色。在高多体病例中;9例中有4例(44.4%)不完全膜性表达,9例中有4例(44.4%)完全膜性表达,9例中有1例(11.1%)胞质表达EGFR.31G7, 8例中有6例(75%)完全膜性表达,6例中有2例(25%)胞质表达EGFR.25。在这里,我们报告了膜性EGFR表达与基因拷贝数增加相关(EGFR. 31g7和EGFR.25克隆的P = 0.035和P = 0.026)。由于在其他系统肿瘤中预测抗EGFR治疗反应的标志物,如EGFR突变和扩增,在乳腺癌中似乎是罕见的事件,因此EGFR的膜染色模式可能是决定患者是否适合抗EGFR治疗的最佳方法。
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EGFR expression and gene copy number in triple-negative breast carcinoma

Most basal-like breast carcinomas are estrogen receptor negative, progesterone receptor negative, and cerb-B2/HER-2/neu negative—the so-called triple-negative breast carcinomas—with high epidermal growth factor receptor (EGFR) expression, which makes EGFR a target of treatment. We evaluated EGFR expression by immunohistochemistry (IHC) with two different clones (EGFR.31G7 and EGFR.25) and gene copy number by fluorescence in situ hybridization (FISH) with Locus specific identifier EGFR/CEP 7 dual probe in 62 triple-negative breast carcinomas. Any complete or incomplete membranous and/or cytoplasmic expression was regarded as IHC positive. Cases showing gene amplification (a ratio of EGFR gene to chromosome 7 of ≥2 or 15 copies per cell in ≥10% of cells) and high polysomy (≥4 copies in ≥40% of cells) were considered FISH positive. We detected EGFR.31G7 positivity in 38 of 62 cases (61.4%), which was composed of 12 of 62 (19.4%) cytoplasmic, 14 of 62 (22.6%) incomplete membranous, and 12 of 62 (19.4%) complete membranous staining. Among 38 of 49 (77.6%) EGFR.25-positive cases, 7 of 49 (14.3%) exhibited cytoplasmic, 10 of 49 (20.4%) exhibited incomplete membranous, and 21 of 49 (42.9%) exhibited complete membranous staining pattern. Ten of 62 (16.1%) FISH-positive cases were identified; 1 of 62 (1.6%) showed amplification, and the rest showed high polysomy. All FISH-positive cases were also found to be IHC positive (P = 0.01) by both EGFR clones. The amplified case displayed strong complete membranous staining with both clones. Among the high polysomic cases; 4 of 9 (44.4%) incomplete membranous, 4 of 9 (44.4%) complete membranous and 1 of 9 (11.1%) cytoplasmic expression of EGFR.31G7, and 6 of 8 (75%) complete membranous and 2 of 6 (25%) cytoplasmic expression of EGFR.25 were detected. Here, we report that membranous EGFR expression is associated with increased gene copy number (P = 0.035 for EGFR.31G7 and P = 0.026 for EGFR.25 clone). Because the markers to predict anti-EGFR treatment response in other system tumors such as EGFR mutation and amplification seem to be rare events in breast cancer, membranous staining pattern of EGFR might be the best way to decide the patient eligibility for anti-EGFR therapy.

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