Rosenthal Eben L, McCrory Allison, Talbert Melissa, Carroll William, Magnuson J Scott, Peters Glenn E
Department of Surgery, Division of Otolaryngology--Head and Neck Surgery, University of Alabama at Birmingham, Birmingham, AL 35249, USA.
Arch Otolaryngol Head Neck Surg. 2004 Aug;130(8):943-7. doi: 10.1001/archotol.130.8.943.
To elucidate tumor-stromal interactions during tumor invasion by assessing the expression of proteolytic enzymes by carcinoma-associated fibroblasts (CAFs) in vivo using complementary DNA (cDNA) array analysis.
Tumor-associated stroma was isolated from tumor and adjacent mucosal specimens of the same patient by laser capture microdissection, and the messenger RNA (mRNA) was assessed by cDNA microarray specific for proteolytic enzymes and their inhibitors. Protein overexpression was then analyzed by immunoblotting of primary fibroblast isolates derived from skin, mucosa, and tumor specimens.
Array analysis of 4 tumor and 4 adjacent mucosal samples demonstrated significant (2.6-fold) overexpression of membrane type 1 matrix metalloproteinase (MT1-MMP) but not of serine proteases or other matrix metalloproteinases. Analysis of normal dermal fibroblasts, normal mucosal fibroblasts, and CAFs similarly demonstrated up-regulation of MT1-MMP.
These results suggest that MT1-MMP mRNA is specifically up-regulated in CAFs in vivo whereas MT1-MMP protein is specifically up-regulated in CAFs in vitro. Known to induce tumor cell invasion when expressed in tumor cells, CAF expression of MT1-MMP may be important in the stromal response to tumor cells that characterizes the desmoplastic reaction.
通过使用互补DNA(cDNA)阵列分析评估体内癌相关成纤维细胞(CAF)中蛋白水解酶的表达,以阐明肿瘤侵袭过程中的肿瘤-基质相互作用。
通过激光捕获显微切割从同一患者的肿瘤和相邻黏膜标本中分离肿瘤相关基质,并通过针对蛋白水解酶及其抑制剂的cDNA微阵列评估信使核糖核酸(mRNA)。然后通过对源自皮肤、黏膜和肿瘤标本的原代成纤维细胞分离物进行免疫印迹分析蛋白过表达情况。
对4个肿瘤样本和4个相邻黏膜样本的阵列分析显示,膜型1基质金属蛋白酶(MT1-MMP)有显著(2.6倍)过表达,但丝氨酸蛋白酶或其他基质金属蛋白酶没有。对正常真皮成纤维细胞、正常黏膜成纤维细胞和CAF的分析同样显示MT1-MMP上调。
这些结果表明,MT1-MMP mRNA在体内CAF中特异性上调,而MT1-MMP蛋白在体外CAF中特异性上调。已知MT1-MMP在肿瘤细胞中表达时可诱导肿瘤细胞侵袭,CAF中MT1-MMP的表达可能在表征促结缔组织增生性反应的基质对肿瘤细胞的反应中起重要作用。