Narayanan B A, Holladay E B, Nixon D W, Mauro C T
Hollings Cancer Center and Department of Medical Laboratory Sciences, Medical University of South Carolina, Charleston, USA.
Life Sci. 1998;63(7):565-73. doi: 10.1016/s0024-3205(98)00307-5.
Retinoids, including natural vitamin A and its analogs, have been closely studied as chemopreventive drugs. The mechanism of action of retinoids, however, is not completely understood. Our study evaluated the effects of all-trans (high affinity ligand for both RAR and RXR receptors) and 9-cis retinoic acid (binds only with RXR receptors) on E6-E7 transcription, cell proliferation, cell cycle distribution, and p53 expression in CaSki cells, a cell line derived from cervical carcinoma containing 600 copies of the HPV-16 genome. Using quantitative RT-PCR analysis, we found that CaSki cells treated with all trans retinoic acid (ATRA) for seven days had a remarkably low level of E6-E7 transcription at 10(-5) M to 10(-9) M concentrations. A smaller inhibitory effect was observed on the E6-E7 transcription at a concentration of 10(-5) M with only 9-cis retinoic acid. Flow cytometric analysis revealed that cells treated with both all trans and 9-cis RA showed an increase in the mean percentage (93.5% and 86.1% respectively) of cells in the G1 phase as compared to untreated CaSki cells (55%) and normal keratinocytes (58%). The percentage of cells in the S phase decreased from a mean percentage of 28 and 26.5 to 5.8 and 5, respectively, after treatment with all trans retinoic acid and 9-cis retinoic acid. An increase in the level of immunophenotypic expression of wild type p53 was also noted after treatment with all trans retinoic acid and 9-cis retinoic acid. All trans and 9-cis retinoic acid may act on highly proliferating tumor cells by initially arresting DNA synthesis and inducing G1 arrest. In addition, they may be inducing a p53 dependent cell cycle arrest and thus suggests that all-trans and 9-cis retinoic acid may have a cytostatic effect rather than a cytotoxic effect on CaSki cells. The increased expression of p53 positive cells and the inhibition of E6/E7 transcription after treatment with these retinoids may indicate the potential role of all trans and 9-cis retinoic acid as a cell cycle regulator and an antiviral chemoprevention agent.
维甲酸,包括天然维生素A及其类似物,作为化学预防药物已得到深入研究。然而,维甲酸的作用机制尚未完全明确。我们的研究评估了全反式维甲酸(对RAR和RXR受体均具有高亲和力的配体)和9-顺式维甲酸(仅与RXR受体结合)对CaSki细胞中E6-E7转录、细胞增殖、细胞周期分布及p53表达的影响。CaSki细胞系源自含有600个HPV-16基因组拷贝的宫颈癌。通过定量RT-PCR分析,我们发现用全反式维甲酸(ATRA)处理7天的CaSki细胞,在10(-5) M至10(-9) M浓度下,E6-E7转录水平显著降低。在10(-5) M浓度下,仅9-顺式维甲酸对E6-E7转录的抑制作用较小。流式细胞术分析显示,与未处理的CaSki细胞(55%)和正常角质形成细胞(58%)相比,用全反式和9-顺式维甲酸处理的细胞G1期细胞平均百分比增加(分别为93.5%和86.1%)。用全反式维甲酸和9-顺式维甲酸处理后,S期细胞百分比分别从平均28%和26.5%降至5.8%和5%。在用全反式维甲酸和9-顺式维甲酸处理后,还观察到野生型p53免疫表型表达水平增加。全反式和9-顺式维甲酸可能通过最初阻止DNA合成并诱导G1期停滞来作用于高度增殖的肿瘤细胞。此外,它们可能诱导p53依赖性细胞周期停滞,因此表明全反式和9-顺式维甲酸对CaSki细胞可能具有细胞生长抑制作用而非细胞毒性作用。用这些维甲酸处理后p53阳性细胞表达增加以及E6/E7转录受到抑制,可能表明全反式和9-顺式维甲酸作为细胞周期调节剂和抗病毒化学预防剂的潜在作用。