Page 199 - Read Online
P. 199

Page 18                Asao et al. Extracell Vesicles Circ Nucleic Acids 2023;4:461-85  https://dx.doi.org/10.20517/evcna.2023.37

               Furthermore, the identification of various EVP-associated biomolecules, including proteins, lipids, and
               nucleic acids, has shed light on their diverse functions and potential as therapeutic targets.

               We can expect groundbreaking discoveries that will redefine our understanding of EVPs and their roles in
               cancer biology for decades to come. The discovery of novel EVP subtypes with unique properties and
               functions will revolutionize diagnostics, prognostics, and therapeutics. Researchers may uncover EVPs
               capable of transporting not just biomolecules, but also energy or information through unconventional
               means, such as quantum communication or other yet-to-be-discovered phenomena. The integration of
               cutting-edge technologies, such as nanotechnology, synthetic biology, and artificial intelligence, will play a
               pivotal role in shaping the future of EVP research. Nanotechnology will enable the creation of hybrid,
               bioengineered EVPs with the ability to self-assemble, replicate, or even harness energy from their
               environment. These smart, programmable EVPs will have unparalleled therapeutic potential, precisely
               navigating complex biological systems, responding to environmental cues, and adapting to the ever-
               changing human body. Synthetic biology will empower researchers to engineer customized EVPs for
               tailored therapeutics, paving the way for personalized medicine in cancer treatment. By leveraging the
               immunomodulatory properties of EVPs, advances in immunotherapy will lead to more effective cancer
               treatments, targeting specific signaling pathways, cellular processes, and even the biophysical properties of
               the extracellular matrix. Artificial intelligence and machine learning systems will revolutionize EVP analysis
               and manipulation, allowing researchers to predict and optimize their behavior in real time. These systems
               will detect subtle patterns and relationships within vast datasets, leading to the identification of novel
               biomarkers and therapeutic targets previously invisible to researchers. The interdisciplinary collaboration
               between researchers in the fields of physics, chemistry, materials science, and engineering will further fuel
               innovation in the EVP-cancer field. For instance, the development of new materials and surfaces for
               efficient EVP isolation and characterization will improve the reproducibility and accuracy of EVP research.
               Moreover, advanced imaging techniques, such as super-resolution microscopy and real-time in vivo
               imaging, will provide invaluable insights into the molecular mechanisms underlying EVP biogenesis, cargo
               packaging, and cellular uptake.

               In conclusion, the EVP-cancer field has made remarkable strides in our understanding of intercellular
               communication and cancer biology. The future of EVP research promises to revolutionize diagnostics,
               prognostics, and therapeutics, with the potential to transform cancer treatment and patient outcomes. As
               we continue to unravel the complex roles of EVPs in health and disease, we will undoubtedly uncover novel
               approaches and applications, reshaping our understanding of the intricate interplay between cells, tissues,
               and organs, and, ultimately, our ability to combat cancer and other devastating diseases.


               DECLARATIONS
               Acknowledgments
               All the figures in this manuscript were created with  BioRender.com

               Authors’ contributions
               Conceived the idea for the manuscript: Lyden D
               Wrote, revised, and edited the manuscript: Asao T, Tobias GC, Lucotti S, Jones DR, Matei I, Lyden D


               Availability of data and materials
               Not applicable.
   194   195   196   197   198   199   200   201   202   203   204