Tissue Array Research Program, Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
J Transl Med. 2011 Jul 29;9:126. doi: 10.1186/1479-5876-9-126.
Head and neck squamous cell carcinoma (HNSCC) still remains a lethal malignancy benefiting from the identification of the new target for early detection and/or development of new therapeutic regimens based on a better understanding of the biological mechanism for treatment. The overexpression of Her2 and Her3 receptors have been identified in various solid tumors, but its prognostic relevance in HNSCC remains controversial.
Three hundred eighty-seven primary HNSCCs, 20 matching metasis and 17 recurrent HNSCCs were arrayed into tissue microarrays. The relationships between Her2 and Her3 protein expression and clinicopathological parameters/survival of HNSCC patients were analyzed with immunohistochemistry.
Her3 is detected as either a cytoplasmic or a membranous dominant expression pattern whereas Her2 expression showed uniform membranous form. In primary tumor tissues, high membranous Her2 expression level was found in 104 (26.9%) cases while positive membranous and cytoplasmic Her3 expression was observed in 34 (8.8%) and 300 (77.5%) samples, respectively. Membranous Her2 expression was significantly associated with histological grade (P = 0.021), as grade 2 tumors showed the highest positive expression. Membranous Her3 over-expression was significantly prevalent in metastatic tissues compared to primary tumors (P = 0.003). Survival analysis indicates that membranous Her3 expression is significantly associated with worse overall survival (P = 0.027) and is an independent prognostic factor in multivariate analysis (hazard ratio, 1.51; 95% confidence interval, 1.01-2.23; P = 0.040).
These results suggest that membranous Her3 expression is strongly associated with poor prognosis of patients with HNSCC and is a potential candidate molecule for targeted therapy.
头颈部鳞状细胞癌(HNSCC)仍然是一种致命的恶性肿瘤,通过识别新的目标,为早期检测和/或开发新的治疗方案提供了帮助,这是基于对治疗生物学机制的更好理解。在各种实体肿瘤中已经发现了 Her2 和 Her3 受体的过表达,但它在 HNSCC 中的预后相关性仍存在争议。
将 387 例原发性 HNSCC、20 例匹配的转移和 17 例复发性 HNSCC 排列成组织微阵列。用免疫组织化学法分析 Her2 和 Her3 蛋白表达与 HNSCC 患者临床病理参数/生存的关系。
Her3 检测到的表达模式主要是细胞质或膜型,而 Her2 表达则呈现均匀的膜型。在原发性肿瘤组织中,104 例(26.9%)病例中发现高膜 Her2 表达水平,而 34 例(8.8%)和 300 例(77.5%)样本中分别观察到阳性膜和细胞质 Her3 表达。膜 Her2 表达与组织学分级显著相关(P = 0.021),2 级肿瘤表现出最高的阳性表达。与原发性肿瘤相比,转移性组织中膜 Her3 过表达更为普遍(P = 0.003)。生存分析表明,膜 Her3 表达与总生存率显著相关(P = 0.027),并在多变量分析中是一个独立的预后因素(危险比,1.51;95%置信区间,1.01-2.23;P = 0.040)。
这些结果表明,膜 Her3 表达与 HNSCC 患者的预后不良密切相关,是靶向治疗的潜在候选分子。