May Felicity E B, Griffin S Michael, Westley Bruce R
Department of Pathology, University of Newcastle upon Tyne, Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne NE1 4LP, UK.
Int J Biochem Cell Biol. 2009 Mar;41(3):632-40. doi: 10.1016/j.biocel.2008.07.015. Epub 2008 Aug 3.
The gastric tumour suppressor trefoil protein TFF1 is present as a covalently bound heterodimer with a previously uncharacterised protein, TFIZ1, in normal human gastric mucosa. The purpose of this research was firstly to examine the molecular forms of TFIZ1 present, secondly to determine if TFIZ1 binds other proteins apart form TFF1 in vivo, thirdly to investigate if TFIZ1 and TFF1 are co-regulated in normal gastric mucosa and fourthly to determine if their co-regulation is maintained or disrupted in gastric cancer. We demonstrate that almost all human TFIZ1 is present as a heterodimer with TFF1 and that TFIZ1 is not bound to either of the other two trefoil proteins, TFF2 and TFF3. TFIZ1 and TFF1 are co-expressed by the surface mucus secretory cells throughout the stomach and the molecular forms of each protein are affected by the relative abundance of the other. TFIZ1 expression is lost consistently, early and permanently in gastric tumour cells. In contrast, TFF1 is sometimes expressed in the absence of TFIZ1 in gastric cancer cells and this expression is associated with metastasis (lymph node involvement: p=0.007). In conclusion, formation of the heterodimer between TFIZ1 and TFF1 is a specific interaction that occurs uniquely in the mucus secretory cells of the stomach, co-expression of the two proteins is disrupted in gastric cancer and expression of TFF1 in the absence of TFIZ1 is associated with a more invasive and metastatic phenotype. This indicates that TFF1 expression in the absence of TFIZ1 expression has potentially deleterious consequences in gastric cancer.
胃肿瘤抑制因子三叶因子蛋白TFF1在正常人胃黏膜中以与一种此前未被鉴定的蛋白TFIZ1共价结合的异二聚体形式存在。本研究的目的,一是检测TFIZ1的存在分子形式,二是确定TFIZ1在体内除了与TFF1结合外是否还与其他蛋白结合,三是研究TFIZ1和TFF1在正常胃黏膜中是否共同调节,四是确定它们的共同调节在胃癌中是维持还是被破坏。我们证明,几乎所有的人TFIZ1都以与TFF1的异二聚体形式存在,且TFIZ1不与另外两种三叶因子蛋白TFF2和TFF3中的任何一种结合。TFIZ1和TFF1在整个胃的表面黏液分泌细胞中共同表达,且每种蛋白的分子形式都受另一种蛋白相对丰度的影响。TFIZ1在胃肿瘤细胞中持续、早期且永久地丢失表达。相比之下,在胃癌细胞中,有时TFF1在没有TFIZ1的情况下表达,且这种表达与转移相关(淋巴结受累:p = 0.007)。总之,TFIZ1和TFF1之间异二聚体的形成是一种独特的相互作用,仅发生在胃的黏液分泌细胞中,这两种蛋白的共同表达在胃癌中被破坏,且在没有TFIZ1的情况下TFF1的表达与更具侵袭性和转移性的表型相关。这表明在胃癌中,在没有TFIZ1表达的情况下TFF1的表达可能产生有害后果。