Lin Julie H, Kim Ellen J, Bansal Anand, Seykora John, Richardson Stephen K, Cha Xian-Yuan, Zafar Sarosh, Nasta Sunita, Wysocka Maria, Benoit Bernice, Rook Alain H, Fakharzadeh Steven S
Department of Dermatology, University of Pennsylvania, Philadelphia 19104, USA.
Blood. 2008 Sep 15;112(6):2484-8. doi: 10.1182/blood-2008-03-141424. Epub 2008 Jun 16.
The oral rexinoid bexarotene (Targretin) is widely used for treatment of cutaneous T-cell lymphomas (CTCL). We recently reported the first case of adult T-cell leukemia/lymphoma (ATLL) that responded rapidly to combination therapy of bexarotene and interferon (IFN)-alpha2b with complete clinical response. We demonstrated that bexarotene induced apoptosis of the patient's malignant peripheral blood T-cells in vitro. However, our patient developed skin and nodal relapse 180 days after starting treatment. We now demonstrate that his peripheral blood malignant T cells became resistant to bexarotene-induced apoptosis. We investigated potential mechanisms that may cause aberrations in the retinoid X receptor (RXR) subunits, RXR-alpha and RXR-beta, to account for these findings. Sequence analysis did not reveal acquisition of mutations in the genes encoding RXR-alpha and RXR-beta by resistant cells. We assessed RXR-alpha and RXR-beta expression by Western blot analysis and found that resistant cells had significantly decreased RXR-alpha expression compared with pretherapy bexarotene-sensitive cells. Our findings indicate that reduced expression of the RXR-alpha receptor subunit may represent a mechanism for resistance to bexarotene in T-cell malignancies.
口服类视黄醛药物贝沙罗汀(他扎罗汀)被广泛用于治疗皮肤T细胞淋巴瘤(CTCL)。我们最近报道了首例对贝沙罗汀与干扰素(IFN)-α2b联合治疗迅速产生反应并获得完全临床缓解的成人T细胞白血病/淋巴瘤(ATLL)病例。我们证明贝沙罗汀在体外可诱导该患者外周血恶性T细胞凋亡。然而,我们的患者在开始治疗180天后出现皮肤和淋巴结复发。我们现在证明其外周血恶性T细胞对贝沙罗汀诱导的凋亡产生了抗性。我们研究了可能导致视黄酸X受体(RXR)亚基RXR-α和RXR-β出现异常从而解释这些发现的潜在机制。序列分析未显示抗性细胞中编码RXR-α和RXR-β的基因发生突变。我们通过蛋白质印迹分析评估了RXR-α和RXR-β的表达,发现与治疗前对贝沙罗汀敏感的细胞相比,抗性细胞的RXR-α表达显著降低。我们的研究结果表明,RXR-α受体亚基表达降低可能是T细胞恶性肿瘤对贝沙罗汀产生抗性的一种机制。