Holtmeier Claudia, Görögh Tibor, Beier Ulf, Meyer Jens, Hoffmann Markus, Gottschlich Stefan, Heidorn Klaus, Ambrosch Petra, Maune Steffen
Department of Otorhinolaryngology, Head and Neck Surgery, University of Kiel, Arnold-Heller-Str. 14, 24105 Kiel, Germany.
Anticancer Res. 2003 May-Jun;23(3B):2585-91.
To compare the mRNA expression profile of head and neck squamous cell carcinoma (HNSCC) cells and normal epithelial cells.
Differential display was used to trace genes showing differential expression in HNSCC cells. Rapid amplification of cDNA ends (RACE) was carried out to identify 5'upstream sequences followed by Northern hybridisation for verification of the differential mRNA expression.
An overexpression of a 59 bp gene fragment was detected in HNSCC cells in contrast to normal epithelial cells. After cloning and sequencing the gene fragment, high grade of homology was found with a human cDNA full insert sequence (fis). After amplification and sequencing of the 5'end of the fis clone, subsequent database searches showed an exact match with the coding sequence of the human lysyl oxidase-like gene 4 (LOXL4). The differential expression of this 4.8 kb LOXL4-mRNA was confirmed by Northern hybridisation.
The data presented in this work might emphasize the involvement of LOXL4 in molecular processes of the genesis or progression of head and neck carcinomas.
比较头颈部鳞状细胞癌(HNSCC)细胞与正常上皮细胞的mRNA表达谱。
采用差异显示技术追踪在HNSCC细胞中表达差异的基因。进行cDNA末端快速扩增(RACE)以鉴定5'上游序列,随后进行Northern杂交以验证差异mRNA表达。
与正常上皮细胞相比,在HNSCC细胞中检测到一个59 bp基因片段的过表达。对该基因片段进行克隆和测序后,发现与人cDNA全插入序列(fis)具有高度同源性。对fis克隆的5'端进行扩增和测序后,随后的数据库搜索显示与人类赖氨酰氧化酶样基因4(LOXL4)的编码序列完全匹配。通过Northern杂交证实了这种4.8 kb LOXL4 - mRNA的差异表达。
本研究呈现的数据可能强调了LOXL4参与头颈部癌发生或进展的分子过程。