Department of Medical Biochemistry, Graduate School of Medicine, University of the Ryukyus, Okinawa 903-0215, Japan.
Biochem Biophys Res Commun. 2010 Aug 27;399(3):365-72. doi: 10.1016/j.bbrc.2010.07.077. Epub 2010 Jul 24.
Cutaneous squamous cell carcinoma (cSCC) results from transformation of epidermal keratinocytes. Invasion of transformed keratinocytes through the basement membrane into the dermis results in invasive cSCC with substantial metastatic potential. To better understand the mechanisms for invasion and metastasis, we compared the protein expression profiles of a non-metastatic transformed mouse keratinocyte line and its metastatic derivative. Keratin 8 (Krt8) and Krt18, not seen in normal keratinocytes, were coexpressed and formed Krt8/18 filaments in the metastatic line. The metastatic line efficiently invaded an artificial basement membrane in vitro owing to the Krt8/18-coexpression, since coexpression of exogenous Krt8/18 in the non-invasive parental line conferred invasiveness. To test whether the Krt8/18-coexpression is induced and is involved in cSCC invasion, we examined specimens from 21 pre-invasive and 24 invasive cSCC patients by immunohistochemistry, and the ectopic Krt8/18-coexpression was almost exclusively found in invasive cSCC. Further studies are needed to examine the clinical significance of ectopic Krt8/18-coexpression in cSCC.
皮肤鳞状细胞癌 (cSCC) 源于表皮角质形成细胞的转化。转化的角质形成细胞通过基底膜侵入真皮,导致具有显著转移潜能的侵袭性 cSCC。为了更好地理解侵袭和转移的机制,我们比较了非转移性转化的小鼠角质形成细胞系及其转移性衍生系的蛋白质表达谱。在正常角质形成细胞中未见的角蛋白 8 (Krt8) 和 Krt18 在转移性系中共同表达并形成 Krt8/18 纤维。由于在非侵袭性亲本系中外源性表达 Krt8/18,转移性系能够有效地在体外侵袭人工基底膜,因为 Krt8/18 的共表达。为了测试 Krt8/18 的共表达是否被诱导并参与 cSCC 的侵袭,我们通过免疫组织化学检查了 21 例前侵袭性和 24 例侵袭性 cSCC 患者的标本,异位 Krt8/18 共表达几乎仅见于侵袭性 cSCC。需要进一步研究异位 Krt8/18 共表达在 cSCC 中的临床意义。