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Microfluidic Applications in Prostate Cancer Research

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Publisher MDPI
Date 2024 Oct 26
PMID 39459070
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Abstract

Prostate cancer is a disease in which cells in the prostate, a gland in the male reproductive system below the bladder, grow out of control and, among men, it is the second-most frequently diagnosed cancer (other than skin cancer). In recent years, prostate cancer death rate has stabilized and, currently, it is the second-most frequent cause of cancer death in men (after lung cancer). Most deaths occur due to metastasis, as cancer cells from the original tumor establish secondary tumors in distant organs. For a long time, classical cell cultures and animal models have been utilized in basic and applied scientific research, including clinical applications for many diseases, such as prostate cancer, since no better alternatives were available. Although helpful in dissecting cellular mechanisms, these models are poor predictors of physiological behavior mainly because of the lack of appropriate microenvironments. Microfluidics has emerged in the last two decades as a technology that could lead to a paradigm shift in life sciences and, in particular, controlling cancer. Microfluidic systems, such as organ-on-chips, have been assembled to mimic the critical functions of human organs. These microphysiological systems enable the long-term maintenance of cellular co-cultures in vitro to reconstitute in vivo tissue-level microenvironments, bridging the gap between traditional cell cultures and animal models. Several reviews on microfluidics for prostate cancer studies have been published focusing on technology advancement and disease progression. As metastatic castration-resistant prostate cancer remains a clinically challenging late-stage cancer, with no curative treatments, we expanded this review to cover recent microfluidic applications related to prostate cancer research. The review includes discussions of the roles of microfluidics in modeling the human prostate, prostate cancer initiation and development, as well as prostate cancer detection and therapy, highlighting potentially major contributions of microfluidics in the continuous march toward eradicating prostate cancer.

References
1.
Novak R, Ingram M, Marquez S, Das D, Delahanty A, Herland A . Robotic fluidic coupling and interrogation of multiple vascularized organ chips. Nat Biomed Eng. 2020; 4(4):407-420. PMC: 8057865. DOI: 10.1038/s41551-019-0497-x. View

2.
Tibbe A, Miller M, Terstappen L . Statistical considerations for enumeration of circulating tumor cells. Cytometry A. 2007; 71(3):154-62. DOI: 10.1002/cyto.a.20369. View

3.
Li R, Hebert J, Lee T, Xing H, Boussommier-Calleja A, Hynes R . Macrophage-Secreted TNFα and TGFβ1 Influence Migration Speed and Persistence of Cancer Cells in 3D Tissue Culture via Independent Pathways. Cancer Res. 2016; 77(2):279-290. PMC: 5243269. DOI: 10.1158/0008-5472.CAN-16-0442. View

4.
Jasuja H, Jaswandkar S, Katti D, Katti K . Interstitial fluid flow contributes to prostate cancer invasion and migration to bone; study conducted using a novel horizontal flow bioreactor. Biofabrication. 2023; 15(2). PMC: 10020972. DOI: 10.1088/1758-5090/acc09a. View

5.
Pattanayak P, Singh S, Gulati M, Vishwas S, Kapoor B, Chellappan D . Microfluidic chips: recent advances, critical strategies in design, applications and future perspectives. Microfluid Nanofluidics. 2021; 25(12):99. PMC: 8547131. DOI: 10.1007/s10404-021-02502-2. View