Thomsen L L, Miles D W, Happerfield L, Bobrow L G, Knowles R G, Moncada S
Wellcome Research Laboratories, Beckenham, Kent, UK.
Br J Cancer. 1995 Jul;72(1):41-4. doi: 10.1038/bjc.1995.274.
Nitric oxide (NO) is generated by a family of isoenzymes (NO synthases) expressed in a wide range of mammalian cells. We have recently reported NO synthase expression in human gynaecological cancers. In this study we have assessed the activity and distribution of NO synthase in a series of human breast tumours and in normal breast tissue. Calcium-dependent (constitutive) and -independent (inducible) NO synthase activity, as well as NO biosynthesis, was high in invasive tumours compared with benign or normal tissue. Furthermore, for invasive ductal carcinomas, NO biosynthesis was significantly greater for grade III compared with grade II tumours. Immunohistochemical investigations revealed immunolabelling with a monoclonal antibody to murine inducible NO synthase predominantly within tumour-associated macrophages. Immunolabelling with a polyclonal antiserum raised against rat brain NO synthase was also observed in vascular endothelial and myoepithelial cells. Thus NO synthase is expressed in human breast tumours, where its presence correlates with tumour grade.
一氧化氮(NO)由在多种哺乳动物细胞中表达的一组同工酶(一氧化氮合酶)产生。我们最近报道了一氧化氮合酶在人类妇科癌症中的表达。在本研究中,我们评估了一系列人类乳腺肿瘤和正常乳腺组织中一氧化氮合酶的活性和分布。与良性或正常组织相比,侵袭性肿瘤中钙依赖性(组成型)和非依赖性(诱导型)一氧化氮合酶活性以及NO生物合成均较高。此外,对于浸润性导管癌,III级肿瘤的NO生物合成明显高于II级肿瘤。免疫组织化学研究显示,用针对小鼠诱导型一氧化氮合酶的单克隆抗体进行免疫标记,主要在肿瘤相关巨噬细胞内。在血管内皮细胞和肌上皮细胞中也观察到用针对大鼠脑一氧化氮合酶的多克隆抗血清进行的免疫标记。因此,一氧化氮合酶在人类乳腺肿瘤中表达,其存在与肿瘤分级相关。