Plaumann Marlies, Seitz Susanne, Frege Renate, Estevez-Schwarz Lope, Scherneck Siegfried
Department of Tumor Genetics, Max Delbrück Center for Molecular Medicine, Robert-Rössle-Str. 10, 13092 Berlin-Buch, Germany.
J Cancer Res Clin Oncol. 2003 Jun;129(6):349-54. doi: 10.1007/s00432-003-0440-z. Epub 2003 May 21.
The chromosome region 8p12-p22 shows frequent allelic loss in many neoplasms, including breast cancer (BC). The DLC-1 gene, located on 8p21-p22, might be a candidate tumor suppressor gene in this region. To evaluate the involvement of DLC-1 in breast carcinogenesis we studied DLC-1 mRNA expression in a panel of 14 primary human BC and the corresponding normal breast cells as well as 8 BC cell lines. Low levels or absence of DLC-1 mRNA were observed in 57% of primary BC and 62.5% of BC cell lines, respectively. We could not find any correlation between DLC-1 mRNA expression and deletions at the DLC-1 locus. Transfection of the gene into DLC-1 deficient T-47D cells raised the DLC-1 mRNA level and resulted in inhibition of cell growth and reduced colony-forming capacity. Our results indicate a role of DLC-1 in BC carcinogenesis.
染色体区域8p12 - p22在包括乳腺癌(BC)在内的许多肿瘤中显示出频繁的等位基因缺失。位于8p21 - p22的DLC - 1基因可能是该区域的一个候选肿瘤抑制基因。为了评估DLC - 1在乳腺癌发生中的作用,我们研究了14例原发性人乳腺癌及相应正常乳腺细胞以及8种乳腺癌细胞系中DLC - 1 mRNA的表达。分别在57%的原发性乳腺癌和62.5%的乳腺癌细胞系中观察到DLC - 1 mRNA水平低或缺失。我们未发现DLC - 1 mRNA表达与DLC - 1基因座缺失之间存在任何相关性。将该基因转染到DLC - 1缺陷的T - 47D细胞中可提高DLC - 1 mRNA水平,并导致细胞生长受到抑制和集落形成能力降低。我们的结果表明DLC - 1在乳腺癌发生中起作用。