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奥滨尤妥珠单抗和利妥昔单抗在滤泡性淋巴瘤 3D 模型中的抗肿瘤活性。

Anti-tumor activity of obinutuzumab and rituximab in a follicular lymphoma 3D model.

机构信息

1] INSERM UMR1037-Centre de Recherche en Cancérologie de Toulouse, Toulouse, France [2] Université Toulouse III Paul-Sabatier, Toulouse, France [3] ERL 5294 CNRS, BP3028, Hôpital Purpan, Toulouse, France [4] Institut Carnot Lymphome-CALYM, Toulouse, France [5] Laboratoire d'Excellence Toulouse Cancer-TOUCAN, Toulouse, France [6] Institut de Recherche Roche, Boulogne Billancourt, France.

出版信息

Blood Cancer J. 2013 Aug 9;3(8):e131. doi: 10.1038/bcj.2013.32.

Abstract

Follicular lymphomas (FLs) account for 35-40% of all adult lymphomas. Treatment typically involves chemotherapy combined with the anti-CD20 monoclonal antibody (MAb) rituximab (RTX). The development of the type II anti-CD20 MAb obinutuzumab (GA101) aims to further improve treatment. Here, using FL cells we show that RTX and GA101 display a similar activity on RL cells cultured in 2D. However, 2D culture cannot mimic tumor spatial organization and conventional 2D models may not reflect the effects of antibodies as they occur in vivo. Thus, we created a non-Hodgkin's lymphoma (NHL) 3D culture system, termed multicellular aggregates of lymphoma cells (MALC), and used it to compare RTX and GA101 activity. Our results show that both antibodies display greater activity towards FL cells in 3D culture compared with 2D culture. Moreover, we observed that in the 3D model GA101 was more effective than RTX both in inhibiting MALC growth through induction of (lysosomal) cell death and senescence and in inhibiting intracellular signaling pathways, such as mammalian target of rapamycin, Akt, PLCgamma (Phospholipase C gamma) and Syk. Altogether, our study demonstrates that spatial organization strongly influences the response to antibody treatment, supporting the use of 3D models for the testing of therapeutic agents in NHL.

摘要

滤泡性淋巴瘤(FL)占所有成人淋巴瘤的 35-40%。治疗通常包括化疗联合抗 CD20 单克隆抗体(MAb)利妥昔单抗(RTX)。开发 II 型抗 CD20 MAb 奥滨尤妥珠单抗(GA101)旨在进一步改善治疗效果。在这里,我们使用 FL 细胞表明,RTX 和 GA101 在二维培养的 RL 细胞上显示出相似的活性。然而,二维培养不能模拟肿瘤的空间组织,传统的二维模型可能无法反映体内发生的抗体作用。因此,我们创建了一个非霍奇金淋巴瘤(NHL)3D 培养系统,称为淋巴瘤细胞的多细胞聚集体(MALC),并使用它来比较 RTX 和 GA101 的活性。我们的结果表明,与二维培养相比,两种抗体在 3D 培养中对 FL 细胞的活性都更高。此外,我们观察到在 3D 模型中,GA101 比 RTX 更有效,既能通过诱导(溶酶体)细胞死亡和衰老来抑制 MALC 生长,又能抑制细胞内信号通路,如哺乳动物雷帕霉素靶蛋白(mTOR)、Akt、PLCγ(磷脂酶 Cγ)和 Syk。总之,我们的研究表明,空间组织强烈影响对抗体治疗的反应,支持使用 3D 模型来测试 NHL 中的治疗剂。

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