Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Mar;48(3):280-289.
doi: 10.1002/cbin.12122. Epub 2024 Jan 15.

The role of exo-miRNA in diagnosis and treatment of cancers, focusing on effective miRNAs in colorectal cancer

Affiliations
Review

The role of exo-miRNA in diagnosis and treatment of cancers, focusing on effective miRNAs in colorectal cancer

Hamzah H Kzar Al-Shukri et al. Cell Biol Int. 2024 Mar.

Abstract

Small extracellular (EV) particles known as exosomes are released by a variety of cell types, including immune system cells, stem cells, and tumor cells. They are regarded as a subgroup of EVs and have a diameter that ranges from 30 to 150 nm. Proteins, lipids, nucleic acids (including RNA and DNA), and different bioactive compounds are among the wide range of biomolecules that make up the cargo of exosomes. Exosomes are crucial for intercellular communication because they let cells share information and signaling chemicals. They are involved in various physiological and pathological processes, including immune responses, tissue regeneration, cancer progression, and neurodegenerative diseases. In conclusion, it is essential to continue research into exosome-based cancer medicines to advance understanding, improve treatment plans, create personalized tactics, ensure safety, and speed up clinical translation.

Keywords: cancer; exosome; extracellular vesicles (EVs); therapeutic approaches.

PubMed Disclaimer

References

REFERENCES

    1. Adhami, M., Haghdoost, A. A., Sadeghi, B., & Malekpour Afshar, R. (2018). Candidate miRNAs in human breast cancer biomarkers: A systematic review. Breast Cancer, 25, 198-205.
    1. Akao, Y., Nakagawa, Y., & Naoe, T. (2006). MicroRNAs 143 and 145 are possible common onco-microRNAs in human cancers. Oncology Reports, 16(4), 845-850.
    1. Albacete-Albacete, L., Navarro-Lérida, I., López, J. A., Martín-Padura, I., Astudillo, A. M., Ferrarini, A., Van-Der-Heyden, M., Balsinde, J., Orend, G., Vázquez, J., & Del Pozo, M. Á. (2020). ECM deposition is driven by caveolin-1-dependent regulation of exosomal biogenesis and cargo sorting. The Journal of Cell Biology, 219(11), e202006178. https://doi.org/10.1083/jcb.202006178
    1. Alles, J., Fehlmann, T., Fischer, U., Backes, C., Galata, V., Minet, M., Hart, M., Abu-Halima, M., Grässer, F. A., Lenhof, H. P., Keller, A., & Meese, E. (2019). An estimate of the total number of true human miRNAs. Nucleic Acids Research, 47(7), 3353-3364. https://doi.org/10.1093/nar/gkz097
    1. Atay, S., & Godwin, A. K. (2014). Tumor-derived exosomes: A message delivery system for tumor progression. Communicative & Integrative Biology, 7(1), e28231. https://doi.org/10.4161/cib.28231

LinkOut - more resources