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Analysis of Cancer Cell Invasion and Anti-metastatic Drug Screening Using Hydrogel Micro-chamber Array HMCA-based Plates
Published on: October 25, 2018
Analysis of Cancer Cell Invasion and Anti-metastatic Drug Screening Using Hydrogel Micro-chamber Array (HMCA)-based
Orit Ravid-Hermesh1, Naomi Zurgil1, Yana Shafran1
1Physics Department, Bar-Ilan University.
Abstract:
Cancer metastasis is known to cause 90% of cancer lethality. Metastasis is a multistage process which initiates with the penetration/invasion of tumor cells into neighboring tissue. Thus, invasion is a crucial step in metastasis, making the invasion process research and development of anti-metastatic drugs, highly significant. To address this demand, there is a need to develop 3D in vitro models which imitate the architecture of solid tumors and their microenvironment most closely to in vivo state on one hand, but at the same time be reproducible, robust and suitable for high yield and high content measurements. Currently, most invasion assays lean on sophisticated microfluidic technologies which are adequate for research but not for high volume drug screening. Other assays using plate-based devices with isolated individual spheroids in each well are material consuming and have low sample size per condition. The goal of the current protocol is to provide a simple and reproducible biomimetic 3D cell-based system for the analysis of invasion capacity in large populations of tumor spheroids. We developed a 3D model for invasion assay based on HMCA imaging plate for the research of tumor invasion and anti-metastatic drug discovery. This device enables the production of numerous uniform spheroids per well (high sample size per condition) surrounded by ECM components, while continuously and simultaneously observing and measuring the spheroids at single-element resolution for medium throughput screening of anti-metastatic drugs. This platform is presented here by the production of HeLa and MCF7 spheroids for exemplifying single cell and collective invasion. We compare the influence of the ECM component hyaluronic acid (HA) on the invasive capacity of collagen surrounding HeLa spheroids. Finally, we introduce Fisetin (invasion inhibitor) to HeLa spheroids and nitric oxide (NO) (invasion activator) to MCF7 spheroids. The results are analyzed by in-house software which enables semi-automatic, simple and fast analysis which facilitates multi-parameter examination.
Insights
This study introduces a novel 3D cell-based system for analyzing tumor cell invasion, crucial for developing anti-metastatic drugs. The platform allows high-throughput screening of numerous uniform spheroids, advancing cancer research.
Area of Science:
- Biomedical Engineering
- Cancer Biology
- Drug Discovery
Background:
- Cancer metastasis is a leading cause of cancer-related deaths, with cellular invasion being a critical step.
- Existing in vitro invasion assays often lack the complexity of in vivo tumor microenvironments or are unsuitable for high-throughput drug screening.
- There is a need for robust, reproducible 3D in vitro models that mimic solid tumors for effective anti-metastatic drug development.
Purpose of the Study:
- To develop a simple, biomimetic 3D cell-based system for analyzing tumor spheroid invasion capacity.
- To enable high-throughput screening of anti-metastatic drugs using a reproducible and scalable assay.
- To provide a platform for studying tumor invasion mechanisms and evaluating potential therapeutic agents.
Main Methods:
- Development of a 3D invasion assay using a high-content imaging (HMCA) plate system.
- Generation of uniform tumor spheroids (HeLa, MCF7) within an extracellular matrix (ECM) environment.
- Continuous, simultaneous observation and measurement of spheroid invasion using specialized software.
Main Results:
- The HMCA plate system facilitates the production of numerous uniform spheroids per well, enabling high sample size per condition.
- The platform successfully demonstrated single-cell and collective invasion of HeLa and MCF7 spheroids.
- The study quantified the influence of hyaluronic acid (HA) on invasion and validated the system with an invasion inhibitor (Fisetin) and activator (nitric oxide, NO).
Conclusions:
- The developed 3D invasion assay platform is suitable for medium-throughput screening of anti-metastatic drugs.
- This biomimetic system offers a reproducible and scalable approach for studying tumor invasion.
- The platform aids in the multi-parameter examination of invasion dynamics and drug efficacy.
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