Gabrielson Edward, Tully Ellen, Hacker Amy, Pegg Anthony E, Davidson Nancy E, Casero Robert A
Department of Pathology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Bunting-Blaustein Cancer Research Building, 1650 Orleans Street, Baltimore, MD 21231-1000, USA.
Cancer Chemother Pharmacol. 2004 Aug;54(2):122-6. doi: 10.1007/s00280-004-0786-1. Epub 2004 May 8.
The polyamine analogue, N1, N11-diethylnorspermine (DENSpm), is currently being evaluated in clinical trials for the treatment of solid tumors. The response of solid tumors to this drug has been associated with superinduction of the polyamine catabolic enzyme, spermine/spermidine N1-acetyltransferase (SSAT). Therefore, to estimate the response of breast cancers to DENSpm, we measured induction of SSAT in breast cancer explants treated in vitro with this polyamine analogue.
Expression of SSAT protein was evaluated by immunohistochemistry in tissue explants from 38 invasive breast cancer tumors incubated in vitro in the presence (or absence) of DENSpm. In addition, SSAT enzymatic activity was measured in tissue explants from four tumors with high cellularity.
SSAT expression was significantly increased in 30 of 38 tumor samples treated with DENSpm compared to untreated controls. This induction of SSAT protein expression was found specifically in neoplastic cells of the treated samples, and was seen in all histologic patterns (ductal, lobular, and mucinous) of breast cancer examined. In tumor samples evaluated for changes in SSAT enzymatic activity, these changes correlated closely with changes in protein expression.
Immunohistochemical staining for induction of SSAT correlates with measures of enzymatic activity in a small sample where measurements were possible and suggests that immunohistochemistry may be used for predicting response of breast cancers to DENSpm. A high proportion of breast cancers induced SSAT in response to DENSpm, supporting the continued consideration of this class of agents for treatment of breast cancer.
多胺类似物N1,N11 - 二乙基亚精胺(DENSpm)目前正在进行实体瘤治疗的临床试验评估。实体瘤对该药物的反应与多胺分解代谢酶精胺/亚精胺N1 - 乙酰转移酶(SSAT)的超诱导有关。因此,为了评估乳腺癌对DENSpm的反应,我们测量了用这种多胺类似物体外处理的乳腺癌外植体中SSAT的诱导情况。
通过免疫组织化学评估38例浸润性乳腺癌肿瘤组织外植体在有(或无)DENSpm存在的情况下体外培养时SSAT蛋白的表达。此外,还测量了来自四个细胞密度高的肿瘤组织外植体的SSAT酶活性。
与未处理的对照相比,在38个用DENSpm处理的肿瘤样本中有30个样本的SSAT表达显著增加。这种SSAT蛋白表达的诱导在处理样本的肿瘤细胞中特异性发现,并且在所检查的所有乳腺癌组织学类型(导管型、小叶型和黏液型)中均可见。在评估SSAT酶活性变化的肿瘤样本中,这些变化与蛋白表达变化密切相关。
在少量可行测量的样本中,SSAT诱导的免疫组织化学染色与酶活性测量相关,表明免疫组织化学可用于预测乳腺癌对DENSpm的反应。高比例的乳腺癌对DENSpm诱导了SSAT,支持继续考虑这类药物用于乳腺癌治疗。