Extracellular vesicles in the development of organ-specific metastasis.
Fumihiko UrabeKalyani PatilGrant A RammTakahiro OchiyaCarolina SoekmadjiPublished in: Journal of extracellular vesicles (2021)
Distant organ metastasis, often termed as organotropic metastasis or metastatic organotropism, is a fundamental feature of malignant tumours and accounts for most cancer-related mortalities. This process is orchestrated by many complex biological interactions and processes that are mediated by a combination of anatomical, genetic, pathophysiological and biochemical factors. Recently, extracellular vesicles (EVs) are increasingly being demonstrated as critical mediators of bi-directional tumour-host cell interactions, controlling organ-specific infiltration, adaptation and colonization at the secondary site. EVs govern organotropic metastasis by modulating the pre-metastatic microenvironment through upregulation of pro-inflammatory gene expression and immunosuppressive cytokine secretion, induction of phenotype-specific differentiation and recruitment of specific stromal cell types. This review discusses EV-mediated metastatic organotropism in visceral (brain, lung, liver, and lymph node) and skeletal (bone) metastasis, and discusses how the pre-metastatic education by EVs transforms the organ into a hospitable, tumour cell-friendly milieu that supports the growth of metastatic cells. Decoding the organ-specific traits of EVs and their functions in organotropic metastasis is essential in accelerating the clinical application of EVs in cancer management.
Keyphrases
- small cell lung cancer
- squamous cell carcinoma
- lymph node
- gene expression
- single cell
- cell therapy
- healthcare
- bone marrow
- skeletal muscle
- poor prognosis
- type diabetes
- insulin resistance
- young adults
- mesenchymal stem cells
- deep learning
- long non coding rna
- metabolic syndrome
- adipose tissue
- bone mineral density
- resting state
- radiation therapy
- functional connectivity
- neoadjuvant chemotherapy
- lymph node metastasis
- brain injury
- squamous cell
- copy number
- white matter
- soft tissue
- body composition
- cell cycle arrest