Brain Tumor Res Treat.  2023 Jan;11(1):8-15. 10.14791/btrt.2022.0045.

Molecular Biology of Brain Metastases

Affiliations
  • 1Department of Cancer Control, National Cancer Center, Graduate School of Cancer Science and Policy. National Cancer Center, Goyang, Korea

Abstract

Brain metastases (BMs) often occur in patients with lung cancer, breast cancer, and melanoma and are the leading cause of morbidity and mortality. The incidence of BM has increased with advanced neuroimaging and prolonged overall survival of cancer patients. With the advancement of local treatment modalities, including stereotactic radiosurgery and navigation-guided microsurgery, BM can be controlled long-term, even in cases with multiple lesions. However, radiation/chemotherapeutic agents are also toxic to the brain, usually irreversibly and cumulatively, and it remains difficult to completely cure BM. Thus, we must understand the molecular events that begin and sustain BM to develop effective targeted therapies and tools to prevent local and distant treatment failure. BM most often spreads hematogenously, and the blood–brain barrier (BBB) presents the first hurdle for disseminated tumor cells (DTCs) entering the brain parenchyma. Nevertheless, how the DTCs cross the BBB and settle on relatively infertile central nervous system tissue remains unknown. Even after successfully taking up residence in the brain, the unique tumor microenvironment is marked by restricted aerobic glycolysis metabolism and limited lymphocyte infiltration. Brain organotropism, certain phenotype of primary cancers that favors brain metastasis, may result from somatic mutation or epigenetic modulation. Recent studies revealed that exosome secretion from primary cancer or over-expression of proteolytic enzymes can “pre-condition” brain vasculoendothelial cells. The concept of the “metastatic niche,” where resident DTCs remain dormant and protected from systemic chemotherapy and antigen exposure before proliferation, is supported by clinical observation of BM in patients clearing systemic cancer and experimental evidence of the interaction between cancer cells and tumor-infiltrating lymphocytes. This review examines extant research on the metastatic cascade of BM through the molecular events that create and sustain BM to reveal clues that can assist the development of effective targeted therapies that treat established BMs and prevent BM recurrence.

Keyword

Brain; Cancer; Metastasis; Tumor microenvironment; Tropism

Figure

  • Fig. 1 Illustration of brain metastatic process. BBB, blood–brain barrier; MTCs, metastatic tumor cells; TAM, tumor-associated macrophages; CTC, circulating tumor cell; ECM, extracellular matrix; BM, brain metastases.

  • Fig. 2 Cancer cell strategy to establish brain metastasis with molecular evidences according to BM process. BM, brain metastases; BBB, blood–brain barrier; TME, tumor microenvironment; EV, extracellular vesicle; TILs, tumor infiltrating lymphocytes; PTEN, phosphatase and tensin homolog.


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