Cañizares F, Salinas J, de las Heras M, Diaz J, Tovar I, Martinez P, Peñafiel R
Department of Clinical Chemistry, Hospital Virgen de la Arrixaca, Murcia, Spain.
Clin Cancer Res. 1999 Aug;5(8):2035-41.
The polyamines putrescine, spermidine, and spermine and ornithine decarboxylase (ODC), the rate-limiting enzyme in their biosynthetic pathway, play an important role in cell proliferation, differentiation, and transformation. In the present study, we have analyzed polyamine concentrations and ODC activity in samples from benign breast diseases (n = 36), benign breast tissue adjacent to the primary carcinoma (n = 19), and breast carcinoma (n = 104). ODC activity in primary carcinoma was significantly higher (2.42 +/- 0.22 nmol CO2/h g; P < 0.001) than that found in benign breast (0.62 +/- 0.15 nmol CO2/h g) or in breast tissue adjacent to the primary carcinoma (0.52 +/- 0.16 nmol CO2/h g). The total polyamine content of breast cancer tissues was higher than in benign breast diseases (704.3 +/- 38.3 nmol/g wet weight versus 295.8 +/- 27.4 nmol/g wet weight) and correlated well with ODC activity (Pearson, r = 0.42; P < 0.001). ODC activity correlated with histological grade, peritumoral lymphatic or blood vessel invasion, S-phase fraction, and cathepsin D. Total polyamine concentration increased with S-phase fraction, cathepsin D, and aneuploidy. No significant correlation was found between ODC or polyamines and tumor size, lymph node involvement, or steroid receptor status. A major finding in our study was that ODC activity was an independent prognostic factor for recurrence and death. The results indicate that the estimation of ODC activity and polyamines in human breast carcinoma might be useful to determine tumor aggressiveness and suggest that ODC may have a potential value as both a prognostic factor and a chemoprevention target in human breast cancer.
多胺腐胺、亚精胺和精胺以及鸟氨酸脱羧酶(ODC)(其生物合成途径中的限速酶)在细胞增殖、分化和转化过程中发挥着重要作用。在本研究中,我们分析了来自良性乳腺疾病(n = 36)、原发性癌旁良性乳腺组织(n = 19)和乳腺癌(n = 104)样本中的多胺浓度和ODC活性。原发性癌中的ODC活性(2.42±0.22 nmol CO2/h g;P < 0.001)显著高于良性乳腺(0.62±0.15 nmol CO2/h g)或原发性癌旁乳腺组织(0.52±0.16 nmol CO2/h g)。乳腺癌组织中的总多胺含量高于良性乳腺疾病(704.3±38.3 nmol/g湿重 vs 295.8±27.4 nmol/g湿重),且与ODC活性密切相关(Pearson相关系数,r = 0.42;P < 0.001)。ODC活性与组织学分级、肿瘤周围淋巴管或血管侵犯、S期分数以及组织蛋白酶D相关。总多胺浓度随S期分数、组织蛋白酶D和非整倍体增加。未发现ODC或多胺与肿瘤大小、淋巴结受累情况或类固醇受体状态之间存在显著相关性。我们研究中的一个主要发现是,ODC活性是复发和死亡的独立预后因素。结果表明,评估人类乳腺癌中的ODC活性和多胺可能有助于确定肿瘤侵袭性,并提示ODC作为人类乳腺癌的预后因素和化学预防靶点可能具有潜在价值。