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Differentially Expressed Genes in Hormone Refractory Prostate Cancer : Association with Chromosomal Regions Involved with Genetic Aberrations

机译:激素难治性前列腺癌中差异表达的基因:与涉及遗传畸变的染色体区域的关联。

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摘要

Differential gene expression between the androgen sensitive human prostate cancer cell line LNCaP and an insensitive clonal variant, LNCaP-r, was demonstrated by suppression subtractive hybridization. Twenty-one sequences were identified of which 9 are homologous to known genes, 11 are represented by expressed sequence tags (ESTs), and 1 is novel. We present data for 5 of 7 sequences confirmed to be differentially expressed by Northern blot analysis and semiquantitative RT-PCR. Only one gene, fibronectin (FN), was highly overexpressed (>60-fold) in LNCaP-r cells, consistent with previously reported overexpression of FN in prostate cancer. Four sequences were down-regulated in LNCaP-r cells, including an inactive variant of the E2 ubiquitin conjugating enzyme (UEV-1), a novel metalloproteinase-related collagenase (PM5), and a potential tumor suppressor gene (breast basic conserved gene, BBC1). UEV-1 is multifunctional, regulates the cell cycle via cdk1, has homology to MMS2 and likewise functions as a DNA protection protein, and also has homology to TSG101. Aberrant splice variants of TSG101 occur frequently in both breast and prostate cancer, but its mechanism of action is unknown. FN, BBC1, and UEV-1 localize to regions of chromosomal aberration (2q3.4, 16q24.3, and 20q13.2, respectively) associated with advanced prostate cancer and thus may be highly relevant to disease progression.
机译:抑制消减杂交法证明了雄激素敏感的人前列腺癌细胞系LNCaP和不敏感的克隆变异体 LNCaP-r之间的差异基因表达。 鉴定出21个序列,其中9个与已知基因同源,11个由表达的序列标签 (ESTs)代表,其中1个是新序列。我们提供了7个序列中的5个的数据 ,通过Northern blot分析 和半定量RT-PCR证实了它们的差异表达。在LNCaP-r细胞中只有一个基因纤连蛋白(FN) 高表达(> 60倍),与先前报道的FN在前列腺癌中的过表达一致。 sup> LNCaP-r细胞中的四个序列被下调,包括 E2泛素结合酶(UEV-1)的失活变体, 金属蛋白酶相关胶原酶(PM5)和潜在的 肿瘤抑制基因(乳腺癌的基本保守基因,BBC1)。 UEV-1 是多功能的,可通过cdk1调节细胞周期,与MMS2具有 同源性,并且还具有DNA保护蛋白的功能, 与TSG101同源。 TSG101 的异常剪接变体在乳腺癌和前列腺癌中均频繁发生,但其 的作用机理尚不清楚。 FN,BBC1和UEV-1将 定位于与晚期前列腺癌相关的染色体畸变区域(分别为2q3.4、16q24.3和20q13.2,分别为 )。因此 可能与疾病进展高度相关。

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  • 来源
    《American Journal of Pathology》 |1999年第5期|1335-1343|共9页
  • 作者单位

    From the Departments of Histopathology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    Surgery,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    From the Departments of Histopathology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    From the Departments of Histopathology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom|and Oncology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    From the Departments of Histopathology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom|and Oncology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    and Oncology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    From the Departments of Histopathology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

    From the Departments of Histopathology,Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom;

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