Redondo M, Concha A, Ruiz-Cabello F, Morell M, Esteban F, Talavera P, Garrido F
Department of Biochemistry, Costa del Sol Hospital, Marbella, Málaga, Spain.
Cancer Detect Prev. 1997;21(1):22-8.
We determined the frequency of expression of the major histocompatibility complex antigens HLA-A,B,C in tumor cells from 207 primary tumor lesions of breast and bronchogenic carcinomas, to see if the expression of theses antigens was linked with several clinicopathological parameters associated with tumor aggressivity, such as abnormal cellular DNA content. We compared tumor tissues with nonneoplastic tissues and tissues from 15 benign breast lesions. HLA class I expressor and nonexpressor tumor cells were determined by using immunohistochemical stains (PAP and APAAP methods) and antibodies against these antigens. Reduction of HLA class I antigen was detected in 65 tumors (31.7%) and was significantly associated with poor tumor differentiation and abnormal cellular DNA content (p < 0.001). These characteristics might define a group of aggressive tumors in which the decrease of HLA class I antigens would enable tumor cells to avoid eliciting host immune responses. On the other hand, the altered regulatory mechanisms, of tumors with abnormal cellular DNA content, might modulate the expression of HLA class I molecules.
我们测定了来自207例乳腺和支气管癌原发肿瘤病灶的肿瘤细胞中主要组织相容性复合体抗原HLA-A、B、C的表达频率,以观察这些抗原的表达是否与一些与肿瘤侵袭性相关的临床病理参数有关,如异常细胞DNA含量。我们将肿瘤组织与非肿瘤组织以及15例乳腺良性病变组织进行了比较。通过使用免疫组织化学染色(PAP和APAAP法)以及针对这些抗原的抗体来确定HLA I类表达和不表达的肿瘤细胞。在65个肿瘤(31.7%)中检测到HLA I类抗原减少,且与肿瘤分化差和异常细胞DNA含量显著相关(p<0.001)。这些特征可能定义了一组侵袭性肿瘤,其中HLA I类抗原的减少会使肿瘤细胞能够避免引发宿主免疫反应。另一方面,具有异常细胞DNA含量的肿瘤其改变的调节机制可能会调节HLA I类分子的表达。