Phenotypic differences of proliferating fibroblasts in the stroma of lung adenocarcinoma and normal bronchus tissue

Fibroblasts in tumor tissue are thought to interact with tumor cells directly and/or indirectly and to have important roles in tumor invasion and metastasis. To characterize the phenotype of proliferating fibroblasts in pulmonary adenocarcinoma, we established short‐term fibroblast cell lines from both normal bronchus and adenocarcinoma tissues obtained from the same patients and compared the gene expression profiles. Four sets of fibroblast cell lines (eight cell lines in total) were used in the analysis. Total RNA was extracted from each cell line and hybridized with 550 cancer‐related RNAs blotted on a cDNA filter array. Five up‐regulated genes and 12 down‐regulated genes (total of 17 genes) were detected in the fibroblast cell lines from the tumor tissues compared with those from normal bronchus. Using real‐time quantitative RT‐PCR methods, the expression profile of each gene was examined; five genes, one up‐regulated (MLH1) and four down‐regulated (Cox1, FGFR4, p120, and Smad3), were confirmed. Furthermore, the protein expression levels of the five genes in the cancerous and normal tissues were examined immunohistochemically, and the up‐regulation of MLH1 and the down‐regulation of Cox1 in cancerous tissue were confirmed in vivo. These results indicate that the proliferating fibroblasts in pulmonary adenocarcinomas are phenotypically different from fibroblasts in normal bronchus tissues.

[1]  T. Miller Protective effects of prostaglandins against gastric mucosal damage: current knowledge and proposed mechanisms. , 1983, The American journal of physiology.

[2]  N. Müller,et al.  Glandular neoplasia of the lung. A proposed analogy to colonic tumors , 1988, Cancer.

[3]  D. McCarthy,et al.  Nonsteroidal anti-inflammatory drugs and peptic ulcer disease. , 1991, Annals of internal medicine.

[4]  C. Torrance,et al.  Gastrointestinal damage associated with the use of nonsteroidal antiinflammatory drugs. , 1992, The New England journal of medicine.

[5]  A. Douglas-Jones,et al.  Epithelial‐stromal interactions in tumors. A morphologic study of fibroepithelial tumors of the breast , 1992, Cancer.

[6]  M. Lippman,et al.  Association of MMP-2 activation potential with metastatic progression in human breast cancer cell lines independent of MMP-2 production. , 1993, Journal of the National Cancer Institute.

[7]  J. Carmichael,et al.  Association between expression of activated 72-kilodalton gelatinase and tumor spread in non-small-cell lung carcinoma. , 1993, Journal of the National Cancer Institute.

[8]  L. Matrisian,et al.  Tumor and stromal expression of matrix metalloproteinases and their role in tumor progression. , 1994, Invasion & metastasis.

[9]  Motoharu Seiki,et al.  A matrix metalloproteinase expressed on the surface of invasive tumour cells , 1994, Nature.

[10]  R. Iozzo Tumor stroma as a regulator of neoplastic behavior. Agonistic and antagonistic elements embedded in the same connective tissue. , 1995, Laboratory investigation; a journal of technical methods and pathology.

[11]  S. Hirohashi,et al.  Small adenocarcinoma of the lung. Histologic characteristics and prognosis. , 1995, Cancer.

[12]  M. Yashiro,et al.  Fibrosis in the peritoneum induced by Scirrhous gastric cancer cells may act as “soil” for peritoneal dissemination , 1996, Cancer.

[13]  N. Maitland,et al.  In vitro modelling of epithelial and stromal interactions in non-malignant and malignant prostates , 2000, British Journal of Cancer.

[14]  T. Tlsty,et al.  Know thy neighbor: stromal cells can contribute oncogenic signals. , 2001, Current opinion in genetics & development.

[15]  R. Weinberg,et al.  Heterotypic signaling between epithelial tumor cells and fibroblasts in carcinoma formation. , 2001, Experimental cell research.

[16]  K. Okuno,et al.  Gene expression analysis in colorectal cancer using practical DNA array filter , 2001, Diseases of the colon and rectum.

[17]  A. Yoshimura,et al.  Altered expression of several genes in highly metastatic subpopulations of a human pulmonary adenocarcinoma cell line. , 2001, European journal of cancer.

[18]  Hepatocarcinoma cell lines down-regulate matrix metalloproteinase-2 expression in human hepatic myofibroblasts. , 2002, International journal of oncology.

[19]  M. Radmacher,et al.  Pitfalls in the use of DNA microarray data for diagnostic and prognostic classification. , 2003, Journal of the National Cancer Institute.

[20]  C. Clelland,et al.  Reduced expression of cyclooxygenase (COX) in idiopathic pulmonary fibrosis and sarcoidosis , 2003, Histopathology.