Applications of Microfluidics and Organ-on-a-Chip in Cancer Research

Biosensors (Basel). 2022 Jun 27;12(7):459. doi: 10.3390/bios12070459.

Abstract

Taking the life of nearly 10 million people annually, cancer has become one of the major causes of mortality worldwide and a hot topic for researchers to find innovative approaches to demystify the disease and drug development. Having its root lying in microelectronics, microfluidics seems to hold great potential to explore our limited knowledge in the field of oncology. It offers numerous advantages such as a low sample volume, minimal cost, parallelization, and portability and has been advanced in the field of molecular biology and chemical synthesis. The platform has been proved to be valuable in cancer research, especially for diagnostics and prognosis purposes and has been successfully employed in recent years. Organ-on-a-chip, a biomimetic microfluidic platform, simulating the complexity of a human organ, has emerged as a breakthrough in cancer research as it provides a dynamic platform to simulate tumor growth and progression in a chip. This paper aims at giving an overview of microfluidics and organ-on-a-chip technology incorporating their historical development, physics of fluid flow and application in oncology. The current applications of microfluidics and organ-on-a-chip in the field of cancer research have been copiously discussed integrating the major application areas such as the isolation of CTCs, studying the cancer cell phenotype as well as metastasis, replicating TME in organ-on-a-chip and drug development. This technology's significance and limitations are also addressed, giving readers a comprehensive picture of the ability of the microfluidic platform to advance the field of oncology.

Keywords: circulating tumor cells; metastasis; microfabrication; microfluidics; organ-on-a-chip; tumor microenvironment.

Publication types

  • Review

MeSH terms

  • Biomimetics
  • Drug Development
  • Humans
  • Lab-On-A-Chip Devices
  • Microfluidics*
  • Neoplasms* / diagnosis
  • Neoplasms* / pathology

Grants and funding

This work was partially supported by a Start-Up Research Grant (SRG2016-00068-FHS) awarded to Kathy Qian Luo from the Faculty of Health Sciences of the University of Macau, Taipa, Macau, China.