4.6 Article

3D Model Characterization by 2D and 3D Imaging in t(14;18)-Positive B-NHL: Perspectives for In Vitro Drug Screens in Follicular Lymphoma

期刊

CANCERS
卷 13, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13071490

关键词

follicular lymphoma; 3D model; spheroid; drug testing; 2D imaging; SPIM

类别

资金

  1. Interreg POCTEFA program [IMLINFO EFA281/16/]
  2. Institut Claudius Regaud CLCC (CIEL) [R20027BB]
  3. iMALC [16003518]
  4. FEDER (iMALC) [16006947/MP0008755]
  5. INSERM
  6. Universite Paul Sabatier
  7. CNRS
  8. ITMO Cancer (Plan Cancer 2014-2019)
  9. CALYM Carnot Institute

向作者/读者索取更多资源

Follicular lymphoma is an incurable type of B cell lymphoproliferative disorder, accounting for a significant percentage of NHL cases. The development of a realistic 3D model offers a promising approach for testing new therapeutic targets.
Simple Summary Follicular lymphoma is an indolent B cell lymphoproliferative disorder of transformed follicular center B cells, which accounts for 20-30 percent of all non-Hodgkin lymphoma (NHL) cases. Although huge efforts have been made in the last 10 years, this pathology is still considered as incurable, leaving open the discovery and testing of new therapeutic targets requiring relevant preclinical models. Here, we report a realistic 3D model of t (14;18)-positive B-NHL cell culture (ultra-low attachment (ULA)-multicellular aggregates of lymphoma cells (MALC)), which monitored by state-of-the-art 2D and 3D imaging, allows more robust drug testing. Follicular lymphoma (FL) is an indolent B cell lymphoproliferative disorder of transformed follicular center B cells, which accounts for 20-30 percent of all non-Hodgkin lymphoma (NHL) cases. Great advances have been made to identify the most relevant targets for precision therapy. However, no relevant models for in vitro studies have been developed or characterized in depth. To this purpose, we generated a 3D cell model from t(14;18)-positive B-NHL cell lines cultured in ultra-low attachment 96-well plates. Morphological features and cell growth behavior were evaluated by classical microscopy (2D imaging) and response to treatment with different drugs was evaluated by a high-content analysis system to determine the robustness of the model. We show that the ultra-low attachment (ULA) method allows the development of regular, spherical and viable ULA-multicellular aggregates of lymphoma cells (MALC). However, discrepancies in the results obtained after 2D imaging analyses on drug-treated ULA-MALC prompted us to develop 3D imaging and specific analyses. We show by using light sheet microscopy and specifically developed 3D imaging algorithms that 3D imaging and dedicated analyses are necessary to characterize morphological properties of 3D models and drug effects. This study proposes a new method, but also imaging tools and informatic solutions, developed for FL necessary for future preclinical studies.

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