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A 3D-Bioprinted Multiple Myeloma Model
Di Wu1, Zongyi Wang1, Jun Li1
1Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA, 02139, USA.
A novel 3D bioprinted model mimics the bone marrow microenvironment for multiple myeloma (MM) research. This advanced model improves cell survival and drug response assessment compared to traditional methods.
Area of Science:
- Biotechnology
- Cancer Research
- Biomedical Engineering
Background:
- Multiple myeloma (MM) is a plasma cell malignancy comprising 12% of hematological cancers.
- Current in vitro models often fail to replicate the complex bone marrow microenvironment, impacting research accuracy.
Purpose of the Study:
- To develop a high-content, 3D in vitro model of multiple myeloma using coaxial extrusion bioprinting.
- To create a human bone marrow-like microenvironment for improved MM cell culture and drug testing.
Main Methods:
- Fabrication of a 3D bioprinted model with a mineral-containing sheath and hydrogel core.
- Co-culture of MM cells with HS5 stromal cells to simulate bone marrow conditions and interleukin-6 (IL-6) release.
- Investigation of bortezomib efficacy and tocilizumab's role in enhancing chemosensitivity via IL-6 receptor inhibition.
Main Results:
- The 3D model demonstrated superior MM cell behavior and drug response compared to 2D cultures.
- Patient-derived MM cells maintained viability for up to 7 days in the 3D model, unlike in planar cultures where they died within 5 days.
- Tocilizumab showed potential in enhancing bortezomib's efficacy by inhibiting IL-6 receptor.
Conclusions:
- A 3D bioprinted multiple myeloma model successfully emulates key bone marrow characteristics.
- This model enhances MM cell proliferation and offers new avenues for drug development and personalized therapy research.
- The study highlights the potential of bioprinting for creating more physiologically relevant cancer models.
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