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Microengineered 3D Tumor Models for Anti-Cancer Drug Discovery in Female-Related Cancers
Farbod Amirghasemi1, Emmanuela Adjei-Sowah1, Barbara A Pockaj2
1School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287-9709, USA.
Abstract:
The burden of cancer continues to increase in society and negatively impacts the lives of numerous patients. Due to the high cost of current treatment strategies, there is a crucial unmet need to develop inexpensive preclinical platforms to accelerate the process of anti-cancer drug discovery to improve outcomes in cancer patients, most especially in female patients. Many current methods employ expensive animal models which not only present ethical concerns but also do not often accurately predict human physiology and the outcomes of anti-cancer drug responsiveness. Conventional treatment approaches for cancer generally include systemic therapy after a surgical procedure. Although this treatment technique is effective, the outcome is not always positive due to various complex factors such as intratumor heterogeneity and confounding factors within the tumor microenvironment (TME). Patients who develop metastatic disease still have poor prognosis. To that end, recent efforts have attempted to use 3D microengineered platforms to enhance the predictive power and efficacy of anti-cancer drug screening, ultimately to develop personalized therapies. Fascinating features of microengineered assays, such as microfluidics, have led to the advancement in the development of the tumor-on-chip technology platforms, which have shown tremendous potential for meaningful and physiologically relevant anti-cancer drug discovery and screening. Three dimensional microscale models provide unprecedented ability to unveil the biological complexities of cancer and shed light into the mechanism of anti-cancer drug resistance in a timely and resource efficient manner. In this review, we discuss recent advances in the development of microengineered tumor models for anti-cancer drug discovery and screening in female-related cancers. We specifically focus on female-related cancers to draw attention to the various approaches being taken to improve the survival rate of women diagnosed with cancers caused by sex disparities. We also briefly discuss other cancer types like colon adenocarcinomas and glioblastoma due to their high rate of occurrence in females, as well as the high likelihood of sex-biased mutations which complicate current treatment strategies for women. We highlight recent advances in the development of 3D microscale platforms including 3D tumor spheroids, microfluidic platforms as well as bioprinted models, and discuss how they have been utilized to address major challenges in the process of drug discovery, such as chemoresistance, intratumor heterogeneity, drug toxicity, etc. We also present the potential of these platform technologies for use in high-throughput drug screening approaches as a replacements of conventional assays. Within each section, we will provide our perspectives on advantages of the discussed platform technologies.
Insights
Developing novel 3D microengineered platforms offers a cost-effective and accurate alternative to animal models for anti-cancer drug discovery. These advanced tumor models accelerate the identification of new treatments, particularly for female-specific cancers.
Area of Science:
- Oncology
- Biomedical Engineering
- Drug Discovery
Background:
- Cancer presents a significant global health burden with high treatment costs.
- Current preclinical models, often animal-based, have limitations in predicting human response and raise ethical concerns.
- There is a critical need for innovative, cost-effective preclinical platforms to improve anti-cancer drug discovery, especially for female patients.
Purpose of the Study:
- To review recent advancements in microengineered tumor models for anti-cancer drug discovery and screening.
- To highlight the potential of these platforms in addressing challenges like chemoresistance and intratumor heterogeneity.
- To focus on applications in female-related cancers and discuss improvements in survival rates due to sex disparities.
Main Methods:
- Review of current literature on 3D microengineered platforms for cancer research.
- Discussion of technologies including 3D tumor spheroids, microfluidic platforms, and bioprinted models.
- Analysis of how these platforms address drug discovery challenges such as chemoresistance, heterogeneity, and toxicity.
Main Results:
- Microengineered assays, particularly tumor-on-chip technology, show promise for physiologically relevant anti-cancer drug screening.
- 3D microscale models offer insights into cancer complexities and drug resistance mechanisms efficiently.
- These platforms can potentially replace conventional assays for high-throughput drug screening.
Conclusions:
- Microengineered tumor models represent a significant advancement in preclinical anti-cancer drug discovery.
- These platforms offer a more predictive, ethical, and cost-effective alternative to traditional methods.
- Further development and application of these technologies are crucial for personalized cancer therapy and improved patient outcomes, especially in female-related cancers.
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