Division of Haematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Br J Haematol. 2010 Jul;150(2):158-69. doi: 10.1111/j.1365-2141.2010.08209.x. Epub 2010 May 9.
Mantle cell lymphoma (MCL) is characterized by translocation t(11;14)(q13;q32), aggressive clinical behaviour, and poor patient outcomes following conventional chemotherapy. New treatment approaches are needed that target novel biological pathways. All trans retinoic acid (ATRA) is a key retinoid that acts through nuclear receptors that function as ligand-inducible transcription factors. The present study evaluated cell killing effects of ATRA-enriched nanoscale delivery particles, termed nanodisks (ND), on MCL cell lines. Results show that ATRA-ND induced cell death more effectively than naked ATRA (dimethyl sulphoxide) or empty ND. ATRA-ND induced reactive oxygen species (ROS) generation to a greater extent than naked ATRA. The antioxidant, N-acetylcysteine, inhibited ATRA-ND induced apoptosis. Compared to naked ATRA, ATRA-ND enhanced G1 growth arrest, up-regulated p21and p27, and down regulated cyclin D1. At ATRA concentrations that induced apoptosis, expression levels of retinoic acid receptor-alpha (RARalpha) and retinoid X receptor-gamma (RXRgamma) were increased. Compared to naked ATRA, ATRA-ND significantly stimulated transcriptional activity of RARA in a model carcinoma cell line. Furthermore, the RAR antagonist, Ro 41-5253, inhibited ATRA-ND induced ROS generation and prevented ATRA-ND induced cell growth arrest and apoptosis. In summary, incorporation of ATRA into ND enhanced the biological activity of this retinoid in cell culture models of MCL.
套细胞淋巴瘤(MCL)的特征是易位 t(11;14)(q13;q32),侵袭性临床行为以及常规化疗后患者预后不良。需要寻求新的治疗方法,以针对新的生物学途径。全反式视黄酸(ATRA)是一种关键的视黄酸,通过核受体起作用,核受体作为配体诱导的转录因子。本研究评估了富含全反式视黄酸的纳米级递送颗粒(称为纳米盘(ND))对 MCL 细胞系的细胞杀伤作用。结果表明,与裸 ATRA(二甲基亚砜)或空 ND 相比,ATRA-ND 更有效地诱导细胞死亡。与裸 ATRA 相比,ATRA-ND 诱导产生的活性氧(ROS)更多。抗氧化剂 N-乙酰半胱氨酸抑制了 ATRA-ND 诱导的细胞凋亡。与裸 ATRA 相比,ATRA-ND 增强了 G1 期生长停滞,上调了 p21 和 p27,并下调了 cyclin D1。在诱导细胞凋亡的 ATRA 浓度下,视黄酸受体-α(RARalpha)和视黄醇 X 受体-γ(RXRgamma)的表达水平增加。与裸 ATRA 相比,ATRA-ND 显著刺激了模型癌细胞系中 RARA 的转录活性。此外,RAR 拮抗剂 Ro 41-5253 抑制了 ATRA-ND 诱导的 ROS 生成,并阻止了 ATRA-ND 诱导的细胞生长停滞和细胞凋亡。总之,将 ATRA 纳入 ND 增强了该视黄酸在 MCL 细胞培养模型中的生物学活性。