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芳烃羟化酶活性是乳腺癌的一种新的预后指标吗?

Is aryl hydrocarbon hydroxylase activity a new prognostic indicator for breast cancer?

作者信息

Pyykkö K, Tuimala R, Aalto L, Perkiö T

机构信息

Department of Clinical Sciences, University of Tampere, Finland.

出版信息

Br J Cancer. 1991 Apr;63(4):596-600. doi: 10.1038/bjc.1991.138.

Abstract

Aryl hydrocarbon hydroxylase (AHH) activity was measured in the breast tumours of 153 primary and 17 recurrent cancer patients, and in 18 patients with benign breast tumour. All operations were carried out in 1983-84. The cytosolic fraction was collected for steroid receptor determination, and microsomes were separated for AHH assay from the same tissue samples. The AHH distribution was wide and highly skewed in all groups. About 10% of the samples showed activities below detection limit. The medians and ranges for primary cancers were 34 (less than 5-2683), for recurrent cancers 40 (20-239) and for benign tumours 11 (less than 5-37) fmol min-1 mg-1 protein. After logarithmic transformation, the mean AHH activities of cancer samples differed significantly from those of benign tumours. The logarithm of AHH activity (log AHH) correlates positively with axillary lymph node status, and negatively with steroid receptor levels. The development of the disease and the survival of the patients were followed for 4 years. The survival and the disease-free interval of the cancer patients who had low AHH activity was significantly higher than that of the high AHH group. The multivariate analysis with Cox's proportional hazad model showed primary tumour size, progesterone receptor concentration, nodal status and log AHH to be the most important independent prognostic factors for survival, while the occurrence of metastases, log AHH and tumour size were the equivalent factors for the disease-free interval in primary breast cancers. We conclude that AHH activity may reflect the overall malignant potential of breast cancer tissue.

摘要

在153例原发性乳腺癌患者、17例复发性乳腺癌患者以及18例良性乳腺肿瘤患者的乳腺肿瘤中检测了芳烃羟化酶(AHH)活性。所有手术均在1983年至1984年进行。收集胞质部分用于类固醇受体测定,并从相同组织样本中分离微粒体用于AHH检测。AHH在所有组中的分布范围广且高度偏态。约10%的样本活性低于检测限。原发性癌的中位数和范围为34(小于5 - 2683),复发性癌为40(20 - 239),良性肿瘤为11(小于5 - 37)fmol min⁻¹ mg⁻¹蛋白质。经对数转换后,癌症样本的平均AHH活性与良性肿瘤的平均AHH活性有显著差异。AHH活性的对数(log AHH)与腋窝淋巴结状态呈正相关,与类固醇受体水平呈负相关。对疾病发展和患者生存情况进行了4年的随访。AHH活性低的癌症患者的生存率和无病生存期显著高于AHH活性高的组。使用Cox比例风险模型进行的多变量分析显示,原发性肿瘤大小、孕激素受体浓度、淋巴结状态和log AHH是生存的最重要独立预后因素,而转移的发生、log AHH和肿瘤大小是原发性乳腺癌无病生存期的等效因素。我们得出结论,AHH活性可能反映乳腺癌组织的总体恶性潜能。

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