Ernst Thomas, Hergenhahn Manfred, Kenzelmann Marc, Cohen Clemens D, Bonrouhi Mahnaz, Weninger Annette, Klären Ralf, Gröne Elisabeth F, Wiesel Manfred, Güdemann Christof, Küster Jens, Schott Winfried, Staehler Gerd, Kretzler Matthias, Hollstein Monica, Gröne Hermann-Josef
Department of Cellular and Molecular Pathology, Deutsches Krebsforschungszentrūm Heidelberg, Heidelberg, Germany.
Am J Pathol. 2002 Jun;160(6):2169-80. doi: 10.1016/S0002-9440(10)61165-0.
Information on over- and underexpressed genes in prostate cancer in comparison to adjacent normal tissue was sought by DNA microarray analysis. Approximately 12,600 mRNA sequences were analyzed from a total of 26 tissue samples (17 untreated prostate cancers, 9 normal adjacent to prostate cancer tissues) obtained by prostatectomy. Hierarchical clustering was performed. Expression levels of 63 genes were found significantly (at least 2.5-fold) increased, whereas expression of 153 genes was decreased (at least 2.5-fold) in prostate cancer versus adjacent normal tissue. In addition to previously described genes such as hepsin, overexpression of several genes was found that has not drawn attention before, such as the genes encoding the specific granule protein (SGP28), alpha-methyl-acyl-CoA racemase, low density lipoprotein (LDL)-phospholipase A2, and the anti-apoptotic gene PYCR1. The radiosensitivity gene ATDC and the genes encoding the DNA-binding protein inhibitor ID1 and the phospholipase inhibitor uteroglobin were significantly down-regulated in the cancer samples. DNA microarray data for eight genes were confirmed quantitatively in five normal and five cancer tissues by real-time reverse transcriptase-polymerase chain reaction with a high correlation between the two methods. Laser capture microdissection of epithelial and stromal compartments from cancer and histological normal specimens followed by an amplification protocol for low levels of RNA (<0.1 microg) allowed us to distinguish between gene expression profiles characteristic of epithelial cells and those typical of stroma. Most of the genes identified in the nonmicrodissected tumor material as up-regulated were indeed overexpressed in cancerous epithelium rather than in the stromal compartment. We conclude that development of prostate cancer is associated with down-regulation as well as up-regulation of genes that show complex differential regulation in epithelia and stroma. Some of the gene expression alterations identified in this study may prove useful in the development of novel diagnostic and therapeutic strategies.
通过DNA微阵列分析寻找前列腺癌中与相邻正常组织相比过表达和低表达基因的信息。从通过前列腺切除术获得的总共26个组织样本(17个未经治疗的前列腺癌、9个前列腺癌相邻的正常组织)中分析了约12,600个mRNA序列。进行了层次聚类。发现63个基因的表达水平显著升高(至少2.5倍),而在前列腺癌与相邻正常组织中,153个基因的表达降低(至少2.5倍)。除了先前描述的基因如组织蛋白酶,还发现了几个以前未引起关注的基因的过表达,如编码特异性颗粒蛋白(SGP28)、α-甲基酰基辅酶A消旋酶、低密度脂蛋白(LDL)-磷脂酶A2的基因以及抗凋亡基因PYCR1。放射敏感性基因ATDC以及编码DNA结合蛋白抑制剂ID1和磷脂酶抑制剂子宫珠蛋白的基因在癌组织样本中显著下调。通过实时逆转录聚合酶链反应在五个正常组织和五个癌组织中对八个基因的DNA微阵列数据进行了定量确认,两种方法之间具有高度相关性。对癌组织和组织学正常标本的上皮和基质成分进行激光捕获显微切割,然后对低水平RNA(<0.1微克)进行扩增方案,使我们能够区分上皮细胞特征性的基因表达谱和基质典型的基因表达谱。在未显微切割的肿瘤材料中鉴定为上调的大多数基因确实在癌上皮中过表达,而不是在基质成分中。我们得出结论,前列腺癌的发生与上皮和基质中显示复杂差异调节的基因的下调以及上调有关。本研究中鉴定的一些基因表达改变可能在新型诊断和治疗策略的开发中证明是有用的。