Ogino Takeshi, Bandoh Nobuyuki, Hayashi Tatsuya, Miyokawa Naoyuki, Harabuchi Yasuaki, Ferrone Soldano
Department of Otolaryngology-Head and Neck Surgery, Asahikawa Medical College, 2-1-1-1 Midorigaoka-Higashi, Asahikawa, Hokkaido 078-8510, Japan.
Clin Cancer Res. 2003 Sep 15;9(11):4043-51.
The purpose of this research was to assess the frequency and clinical significance of antigen processing machinery component and HLA class I antigen down-regulation in primary maxillary sinus squamous cell carcinoma (SCC) lesions.
Formalin-fixed, paraffin-embedded tumor biopsy specimens at pretreatment status from 70 Japanese patients with maxillary sinus SCC were examined for HLA class I antigen and endoplasmic reticulum chaperone molecule expression using an immunohistochemical method. Furthermore, the results of immunohistochemical staining of the lesions were correlated with their histopathological characteristics and with the clinical course of the disease.
Calnexin, ERp57, calreticulin, tapasin, and HLA class I antigens were down-regulated in 13, 13, 24, 69, and 78% of the 70 lesions tested, respectively. Both tapasin and HLA class I antigen expression were significantly correlated with the number of infiltrating CD3(+) T cells into tumor lesions (P < 0.01); furthermore, tapasin expression was significantly correlated with tumor differentiation (P = 0.024). Tapasin expression was correlated with that of HLA class I antigens (P < 0.01). Furthermore, tapasin and HLA class I antigen down-regulation in SCC lesions was significantly associated with reduced survival of patients (P = 0.01 and P = 0.002, respectively). Multivariate Cox proportional hazards model analysis identified HLA class I antigen down-regulation as an independent prognostic marker.
Tapasin expression appears to be associated with HLA class I antigen expression in primary maxillary sinus SCC lesions. Furthermore, defects in tapasin and HLA class I antigen expression in primary maxillary sinus SCC lesions may play a role in the clinical course of the disease, because these defects were associated with poor prognosis.
本研究旨在评估原发性上颌窦鳞状细胞癌(SCC)病变中抗原加工机制成分及HLA - I类抗原下调的频率和临床意义。
采用免疫组织化学方法,对70例日本上颌窦SCC患者治疗前状态的福尔马林固定、石蜡包埋肿瘤活检标本进行HLA - I类抗原和内质网伴侣分子表达检测。此外,将病变的免疫组织化学染色结果与其组织病理学特征及疾病临床进程相关联。
在所检测的70个病变中,钙连接蛋白、内质网蛋白57、钙网蛋白、塔帕辛和HLA - I类抗原的下调率分别为13%、13%、24%、69%和78%。塔帕辛和HLA - I类抗原的表达均与肿瘤病变中浸润的CD3(+) T细胞数量显著相关(P < 0.01);此外,塔帕辛表达与肿瘤分化显著相关(P = 0.024)。塔帕辛表达与HLA - I类抗原表达相关(P < 0.01)。此外,SCC病变中塔帕辛和HLA - I类抗原下调与患者生存率降低显著相关(分别为P = 0.01和P = 0.002)。多变量Cox比例风险模型分析确定HLA - I类抗原下调为独立的预后标志物。
在原发性上颌窦SCC病变中,塔帕辛表达似乎与HLA - I类抗原表达相关。此外,原发性上颌窦SCC病变中塔帕辛和HLA - I类抗原表达缺陷可能在疾病临床进程中起作用,因为这些缺陷与预后不良相关。