Dutsch-Wicherek Magdalena, Sikora Jerzy, Tomaszewska Romana
Department of Otolaryngology, Head and Neck Surgery of the Jagiellonian University, Krakow, Poland.
Front Biosci. 2008 May 1;13:4029-38. doi: 10.2741/2991.
Metallothioneins (MTs) are a family of low molecular weight proteins with a high affinity for divalent metals. Metallothionein has been shown to have a protective role in apoptosis. Specifically, it controls the cellular zinc ion levels. The proper intracellular Zn2+ level maintains the fragmentation of DNA associated with caspase-3 activity. In cancer nests, MT has been identified in the peripheral regions and associated with higher cell proliferation rates and fewer positive apoptotic cells. The expression of MT in the stroma has been linked with tumor spread. The tumor stroma may respond to tumor growth and aggressiveness by the expression of MT, thus protecting itself from and developing a resistance to apoptosis. Multistep carcinogenesis is related to a breakdown in immune response that enables tumor progression and dissemination. This breakdown is a crucial for tumor survival. The evaluation of MT expression in cancer and its stroma seems to correlate with the level of immune system inhibition in cancer-adjacent stroma.
金属硫蛋白(MTs)是一类对二价金属具有高亲和力的低分子量蛋白质。金属硫蛋白已被证明在细胞凋亡中具有保护作用。具体而言,它控制细胞内锌离子水平。适当的细胞内锌离子水平维持与半胱天冬酶-3活性相关的DNA片段化。在癌巢中,MT已在外周区域被鉴定出来,并与较高的细胞增殖率和较少的阳性凋亡细胞相关。MT在基质中的表达与肿瘤扩散有关。肿瘤基质可能通过MT的表达对肿瘤生长和侵袭性做出反应,从而保护自身免受凋亡并产生抗凋亡能力。多步骤致癌作用与免疫反应的破坏有关,这种破坏使肿瘤得以进展和扩散。这种破坏对肿瘤存活至关重要。评估MT在癌症及其基质中的表达似乎与癌旁基质中免疫系统抑制水平相关。