Extracellular vesicles in breast cancer drug resistance and their clinical application

Shentong Yu1,2, Yifang Wei1, Yuqiao Xu3

  • 1Department of Biochemistry and Molecular Biology, State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, 710032, China.

Insights

Extracellular vesicles (EVs) play a key role in breast cancer drug resistance by carrying miRNAs and proteins. These EVs also offer potential for diagnostics and targeted cancer therapy.

Area of Science:

  • Oncology
  • Cell Biology
  • Biochemistry

Background:

  • Drug resistance is a major obstacle in breast cancer treatment.
  • Extracellular vesicles (EVs) are increasingly recognized for their role in mediating chemo-insensitivity.
  • EVs contain diverse cargo, including miRNAs and proteins, influencing cellular functions.

Purpose of the Study:

  • To review the mechanisms linking EVs to breast cancer drug resistance.
  • To summarize recent advancements in the clinical applications of EVs in breast cancer.

Main Methods:

  • Literature review of studies on extracellular vesicles and breast cancer drug resistance.
  • Analysis of mechanisms involving EV cargo (miRNAs, proteins) in chemoresistance.
  • Evaluation of current and emerging clinical applications of EVs.

Main Results:

  • EVs, through their miRNA and protein cargo, significantly contribute to both de novo and acquired drug resistance in breast cancer.
  • Advances in EV extraction and detection enable their use in diagnostics and predicting therapeutic outcomes.
  • EVs show promise as drug delivery systems for future anticancer therapies.

Conclusions:

  • Extracellular vesicles are critical mediators of breast cancer drug resistance.
  • EVs hold significant potential for improving breast cancer diagnosis, prognosis, and treatment strategies.

Related Concept Videos

Overview of Exosomes01:36

Overview of Exosomes

Exosomes are stable, lipid bilayer-enclosed vesicles capable of crossing biological barriers. They can carry a wide range of molecules required for intercellular communication. Once exosomes are released from the cell where they originated, they enter a recipient cell through various pathways such as fusion, receptor-mediated endocytosis, macropinocytosis, and phagocytosis.
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...
3.9K
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.9K
Metastasis02:30

Metastasis

Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
6.8K