Rought S E, Yau P M, Schnier J B, Chuang L F, Chuang R Y
Department of Medical Pharmacology and Toxicology, School of Medicine, University of California, Davis 95616, USA.
Toxicol Lett. 1998 Jan 16;94(1):29-36. doi: 10.1016/s0378-4274(97)00096-9.
Previous studies have shown that heptachlor, a chlorinated hydrocarbon insecticide, is a liver tumor promoter in rats and mice and induces tumor promoting-like alterations in human myeloblastic leukemia cells. The nature of tumor promotion is multifaceted and has recently been shown to include suppression of programmed cell death (apoptosis) as a mechanism by which a tumor promoter can prolong cell viability. The ability of tumor promoters to suppress apoptosis prompted us to address the question of whether heptachlor is capable of effecting the expression of genes involved in lymphocyte apoptosis, in particular, the p53 tumor suppressor gene. Experiments with a CEM x 174 cell line, a hybrid of human T and B cells, revealed that heptachlor downregulated p53 gene expression at the post-transcriptional level without changing levels of mRNA in the cells. The heptachlor-induced reduction in the basal levels of expression of this gene was both in a concentration and time-dependent manner.
以往的研究表明,七氯这种氯化烃类杀虫剂是大鼠和小鼠的肝脏肿瘤促进剂,并能在人髓性白血病细胞中诱导类似肿瘤促进的改变。肿瘤促进的性质是多方面的,最近已表明其机制包括抑制程序性细胞死亡(凋亡),肿瘤促进剂可通过这种机制延长细胞活力。肿瘤促进剂抑制凋亡的能力促使我们探讨七氯是否能够影响参与淋巴细胞凋亡的基因表达,特别是p53肿瘤抑制基因。用人T细胞和B细胞杂交的CEM x 174细胞系进行的实验表明,七氯在转录后水平下调p53基因表达,而不改变细胞中的mRNA水平。七氯诱导该基因基础表达水平的降低呈浓度和时间依赖性。