Kirikoshi H, Sekihara H, Katoh M
Genetics and Cell Biology Section, Genetics Division, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
Int J Oncol. 2001 Jul;19(1):111-5.
Human Frizzled-7 (FZD7) and human FzE3, showing 98.8% nucleotide identity, encode almost identical WNT receptors with nine amino-acid substitutions. FzE3 is claimed to be expressed specifically in esophageal cancer. We determined the structure of the FZD7 gene and the FZD7 cDNA expressed in esophageal cancer. The FZD7 gene without intron and the FZD7 cDNAs isolated from esophageal cancer cell lines TE4 and TE5 were found to encode WNT receptor identical to FZD7, but not to FzE3. Nucleotide sequence of FzE3 was not identified on the human genome draft sequence. Thus, we could not obtain any data suggesting the existence of FzE3. Expression profile of FZD7 was also investigated. FZD7 was expressed throughout normal gastrointestinal tract, from esophagus to rectum. Among human esophageal and gastric cancer cell lines, expression level of FZD7 was relatively lower in esophageal cancer cell lines, and was highest in the gastric cancer cell line MKN7. FZD7 was up-regulated in one out of six cases of human primary gastric cancer. As over-expression of Frizzled-7 leads to activation of the WNT-beta-catenin-TCF pathway, up-regulation of FZD7 in human gastric cancer might play key roles in carcinogenesis through activation of the WNT-beta-catenin-TCF pathway.
人类卷曲蛋白-7(FZD7)与人类FzE3的核苷酸同一性为98.8%,编码几乎相同的WNT受体,仅有9个氨基酸替换。据称FzE3在食管癌中特异性表达。我们确定了FZD7基因以及在食管癌中表达的FZD7 cDNA的结构。发现不含内含子的FZD7基因以及从食管癌细胞系TE4和TE5中分离出的FZD7 cDNA编码的WNT受体与FZD7相同,而非FzE3。在人类基因组草图序列上未鉴定出FzE3的核苷酸序列。因此,我们无法获得任何表明FzE3存在的数据。我们还研究了FZD7的表达谱。FZD7在从食管到直肠的整个正常胃肠道中均有表达。在人类食管和胃癌细胞系中,FZD7的表达水平在食管癌细胞系中相对较低,在胃癌细胞系MKN7中最高。在6例人类原发性胃癌病例中,有1例FZD7表达上调。由于卷曲蛋白-7的过表达会导致WNT-β-连环蛋白-TCF信号通路激活,因此FZD7在人类胃癌中的上调可能通过激活WNT-β-连环蛋白-TCF信号通路在致癌过程中发挥关键作用。