Jin Rongxian, Huang Jingxiang, Tan Puay-Hoon, Bay Boon-Huat
Department of Anatomy, National University of Singapore.
Pathol Oncol Res. 2004;10(2):74-9. doi: 10.1007/BF02893459. Epub 2004 Jun 9.
Metallothioneins (MTs) are a family of metal binding proteins that play an important role in maintaining transition metal ion homoeostasis, redox balance in the cell and fundamental cellular processes such as proliferation and apoptosis. In humans, there are 4 groups of MT proteins which are encoded by 10 functional MT isoforms. In breast tissues, MT is primarily expressed in myoepithelial and malignant epithelial cells. Immunohistochemical studies have revealed that 26% to 100% of invasive ductal breast cancers express the MT protein. The MT-1F and MT-2A isoforms have been reported to be associated with higher histological grade in breast cancer, whereas higher MT-1E mRNA expression was found in estrogen receptor-negative tumors compared to their estrogen receptor-positive counterparts. A number of studies have shown that MT expression in breast cancer is associated with poorer prognosis. In addition, metallothionein expression may have a potential role in protecting the breast cancer cell from chemotherapeutic threats to survival.
金属硫蛋白(MTs)是一类金属结合蛋白,在维持过渡金属离子稳态、细胞内氧化还原平衡以及细胞增殖和凋亡等基本细胞过程中发挥着重要作用。在人类中,有4组MT蛋白,由10种功能性MT异构体编码。在乳腺组织中,MT主要表达于肌上皮细胞和恶性上皮细胞。免疫组织化学研究表明,26%至100%的浸润性导管乳腺癌表达MT蛋白。据报道,MT-1F和MT-2A异构体与乳腺癌较高的组织学分级相关,而与雌激素受体阳性肿瘤相比,雌激素受体阴性肿瘤中MT-1E mRNA表达更高。许多研究表明,乳腺癌中MT的表达与较差的预后相关。此外,金属硫蛋白的表达可能在保护乳腺癌细胞免受化疗对生存的威胁方面具有潜在作用。