Karagianni Fani, Piperi Christina, Valero-Diaz Sara, Amato Camilla, Vaque Jose Pedro, Casar Berta, Papadavid Evangelia
National Center of Rare Diseases-Cutaneous Lymphoma, Second Department of Dermatology and Venereal Diseases, Attikon University General Hospital, National and Kapodistrian University of Athens, 12462 Athens, Greece.
Department of Biological Chemistry, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Cancers (Basel). 2024 Sep 17;16(18):3176. doi: 10.3390/cancers16183176.
Angiogenesis plays a pivotal role in the growth and metastasis of tumors, including the development and progression of cutaneous lymphomas. The chick embryo CAM model has been utilized in various studies to assess the growth rate, angiogenic potential, and metastatic capability of different tumor types and malignant cell lines. However, the precise mechanisms of angiogenesis in CTCL and the influence of Ruxolitinib or Resminostat on angiogenesis in hematological malignancies and solid tumors are not well understood. Recent in vitro and in vivo data have demonstrated the synergistic inhibition of tumorigenesis and metastasis in experimental models of CTCL when using the combination of Resminostat (HDACi) with Ruxolitinib (JAKi). The present work aims to elucidate the effects of this combination on the tumor microenvironment's vascular components. We investigated the effects of Ruxolitinib (JAKi) in combination with Resminostat (HDACi) treatment in transendothelial migration of CTCL cells (10 MyLa and SeAx) by using a transwell-based transendothelial migration assay and tumor angiogenesis in vivo. We used the CTCL chick embryo CAM model with xenografted tumors derived from implanted MyLa and SeAx cells and administered topically 15 μM ruxolitinib and 5 μM Resminostat every two days during a 5-day period. JAKi and HDACi inhibited CTCL cell transendothelial migration by 75% and 82% ( < 0.05) in both CTCL engrafted cells (MyLa and SeAx, respectively) compared to the untreated group. Moreover, the combination of ruxolitinib with resminostat blocked angiogenesis by significantly reducing the number of blood vessel formation by 49% and 34% in both MyLa and SeAx, respectively ( < 0.05), indicating that the proposed combination exerted significant anti-angiogenic effects in the CAM CTCL model. Overall, these data provide valuable insights into potential therapeutic strategies targeting angiogenesis in CTCL, paving the way for more effective treatment approaches in the future.
血管生成在肿瘤的生长和转移中起着关键作用,包括皮肤淋巴瘤的发生和发展。鸡胚绒毛尿囊膜(CAM)模型已被用于各种研究,以评估不同肿瘤类型和恶性细胞系的生长速率、血管生成潜力和转移能力。然而,蕈样肉芽肿(CTCL)中血管生成的确切机制以及鲁索替尼或雷斯那司他对血液系统恶性肿瘤和实体瘤血管生成的影响尚未完全明确。最近的体外和体内数据表明,在CTCL的实验模型中,当使用雷斯那司他(组蛋白去乙酰化酶抑制剂,HDACi)与鲁索替尼(Janus激酶抑制剂,JAKi)联合使用时,对肿瘤发生和转移具有协同抑制作用。本研究旨在阐明这种联合用药对肿瘤微环境血管成分的影响。我们通过基于Transwell的跨内皮迁移试验,研究了鲁索替尼(JAKi)与雷斯那司他(HDACi)联合治疗对CTCL细胞(10 MyLa和SeAx)跨内皮迁移的影响以及对体内肿瘤血管生成的影响。我们使用了接种了源自植入的MyLa和SeAx细胞的异种移植肿瘤的CTCL鸡胚CAM模型,并在5天的时间内每两天局部给予15 μM鲁索替尼和5 μM雷斯那司他。与未治疗组相比,JAKi和HDACi分别使两种CTCL植入细胞(MyLa和SeAx)的跨内皮迁移率降低了75%和82%(P<0.05)。此外,鲁索替尼与雷斯那司他的联合用药通过分别使MyLa和SeAx中的血管形成数量显著减少49%和34%(P<0.05)来阻断血管生成,表明该联合用药在CAM CTCL模型中发挥了显著的抗血管生成作用。总体而言,这些数据为CTCL中针对血管生成的潜在治疗策略提供了有价值的见解,为未来更有效的治疗方法铺平了道路。