Molecular Biology Laboratory, Department of Otolaryngology, Head and Neck Surgery, University of Heidelberg, Heidelberg, Germany.
Arch Physiol Biochem. 2010 Oct-Dec;116(4-5):218-26. doi: 10.3109/13813455.2010.525240. Epub 2010 Nov 17.
We reasoned that micro-dissection of tumour cells for protein expression studies should be omitted since tumour-stroma interactions are an important part of the biology of solid tumours. To study such interactions in head and neck squamous cell carcinoma (HNSCC) development, we generated reference protein spectra for normal squamous epithelium and connective tissue by SELDI-TOF-MS. Calgranulins A and B, Annexin1 and Histone H4 were found to be strongly enriched in the epithelium. The alpha-defensins 1-3 and the haemoglobin subunits were identified in the connective tissue. Tumour-distant epithelia, representing early pre-malignant lesions, showed up-regulated expression of the stromal alpha-defensins, whereas the epithelial Annexin 1 was down-regulated. Thus, tumour microenvironment interactions occur very early in the carcinogenic process. These data demonstrate that omitting micro-dissection is actually beneficial for studying changes in protein expression during development and progression of solid tumours.
我们推断,由于肿瘤-基质相互作用是实体瘤生物学的重要组成部分,因此应该省略肿瘤细胞的微量解剖用于蛋白质表达研究。为了研究头颈部鳞状细胞癌 (HNSCC) 发展中的这种相互作用,我们通过 SELDI-TOF-MS 为正常鳞状上皮和结缔组织生成了参考蛋白图谱。发现钙粒蛋白 A 和 B、膜联蛋白 1 和组蛋白 H4 在上皮组织中强烈富集。α-防御素 1-3 和血红蛋白亚基在结缔组织中被鉴定出来。代表早期癌前病变的肿瘤远处上皮显示基质α-防御素的上调表达,而上皮膜联蛋白 1 下调。因此,肿瘤微环境相互作用在致癌过程的早期就发生了。这些数据表明,省略微解剖实际上有利于研究实体瘤发生和发展过程中蛋白质表达的变化。