Molecular and cellular mechanisms underlying brain metastasis of breast cancer

被引:105
|
作者
Hosonaga, Mari [1 ,2 ]
Saya, Hideyuki [1 ]
Arima, Yoshimi [1 ]
机构
[1] Keio Univ, Sch Med, Inst Adv Med Res, Div Gene Regulat,Shinjuku Ku, 35 Shinano Machi, Tokyo 1608582, Japan
[2] Japanese Fdn Canc Res, Canc Inst Hosp, Breast Med Oncol Dept, Koto Ku, 3-8-31 Ariake, Tokyo 1358550, Japan
关键词
Breast cancer; Brain metastasis; Astrocyte; STAT3; PI3K-Akt; xCT; GRADED PROGNOSTIC ASSESSMENT; TUMOR-CELLS; SURVIVAL; INHIBITION; MELANOMA; GROWTH; SULFASALAZINE; COMBINATION; TRANSPORTER; PORTRAITS;
D O I
10.1007/s10555-020-09881-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis of cancer cells to the brain occurs frequently in patients with certain subtypes of breast cancer. In particular, patients with HER2-positive or triple-negative breast cancer are at high risk for the development of brain metastases. Despite recent advances in the treatment of primary breast tumors, the prognosis of breast cancer patients with brain metastases remains poor. A better understanding of the molecular and cellular mechanisms underlying brain metastasis might be expected to lead to improvements in the overall survival rate for these patients. Recent studies have revealed complex interactions between metastatic cancer cells and their microenvironment in the brain. Such interactions result in the activation of various signaling pathways related to metastasis in both cancer cells and cells of the microenvironment including astrocytes and microglia. In this review, we focus on such interactions and on their role both in the metastatic process and as potential targets for therapeutic intervention.
引用
收藏
页码:711 / 720
页数:10
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