Melanoma Brain Metastasis: Mechanisms, Models, and Medicine

被引:46
作者
Kircher, David A. [1 ]
Silvis, Mark R. [2 ]
Cho, Joseph H. [1 ]
Holmen, Sheri L. [1 ,2 ,3 ]
机构
[1] Univ Utah, Dept Oncol Sci, Hlth Sci Ctr, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Surg, Hlth Sci Ctr, Salt Lake City, UT 84112 USA
[3] Univ Utah, Huntsman Canc Inst, Hlth Sci Ctr, Salt Lake City, UT 84112 USA
关键词
melanoma; brain metastases; mechanisms; models; clinical trials; GRADED PROGNOSTIC ASSESSMENT; ENDOTHELIAL GROWTH-FACTOR; MALIGNANT-MELANOMA; RADIATION-THERAPY; OPEN-LABEL; STEREOTACTIC RADIOSURGERY; EXTRACELLULAR S100A4; BREAST-CANCER; PROMOTES DEVELOPMENT; PI3K PATHWAY;
D O I
10.3390/ijms17091468
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of brain metastases in patients with advanced stage melanoma is common, but the molecular mechanisms responsible for their development are poorly understood. Melanoma brain metastases cause significant morbidity and mortality and confer a poor prognosis; traditional therapies including whole brain radiation, stereotactic radiotherapy, or chemotherapy yield only modest increases in overall survival (OS) for these patients. While recently approved therapies have significantly improved OS in melanoma patients, only a small number of studies have investigated their efficacy in patients with brain metastases. Preliminary data suggest that some responses have been observed in intracranial lesions, which has sparked new clinical trials designed to evaluate the efficacy in melanoma patients with brain metastases. Simultaneously, recent advances in our understanding of the mechanisms of melanoma cell dissemination to the brain have revealed novel and potentially therapeutic targets. In this review, we provide an overview of newly discovered mechanisms of melanoma spread to the brain, discuss preclinical models that are being used to further our understanding of this deadly disease and provide an update of the current clinical trials for melanoma patients with brain metastases.
引用
收藏
页数:29
相关论文
共 193 条
[1]   Structure and function of the blood-brain barrier [J].
Abbott, N. Joan ;
Patabendige, Adjanie A. K. ;
Dolman, Diana E. M. ;
Yusof, Siti R. ;
Begley, David J. .
NEUROBIOLOGY OF DISEASE, 2010, 37 (01) :13-25
[2]   Connexin43 Reduces Melanoma Growth within a Keratinocyte Microenvironment and during Tumorigenesis in Vivo [J].
Ableser, Mark J. ;
Penuela, Silvia ;
Lee, Jack ;
Shao, Qing ;
Laird, Dale W. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (03) :1592-1603
[3]   Temozolomide for the treatment of brain metastases associated with metastatic melanoma: A phase II study [J].
Agarwala, SS ;
Kirkwood, JM ;
Gore, M ;
Dreno, B ;
Thatcher, N ;
Czarnetski, B ;
Atkins, M ;
Buzaid, A ;
Skarlos, D ;
Rankin, EM .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (11) :2101-2107
[4]   Clinical outcomes of melanoma brain metastases treated with stereotactic radiation and anti-PD-1 therapy [J].
Ahmed, K. A. ;
Stallworth, D. G. ;
Kim, Y. ;
Johnstone, P. A. S. ;
Harrison, L. B. ;
Caudell, J. J. ;
Yu, H. H. M. ;
Etame, A. B. ;
Weber, J. S. ;
Gibney, G. T. .
ANNALS OF ONCOLOGY, 2016, 27 (03) :434-441
[5]   Genomic Classification of Cutaneous Melanoma [J].
Akbani, Rehan ;
Akdemir, Kadir C. ;
Aksoy, B. Arman ;
Albert, Monique ;
Ally, Adrian ;
Amin, Samirkumar B. ;
Arachchi, Harindra ;
Arora, Arshi ;
Auman, J. Todd ;
Ayala, Brenda ;
Baboud, Julien ;
Balasundaram, Miruna ;
Balu, Saianand ;
Barnabas, Nandita ;
Bartlett, John ;
Bartlett, Pam ;
Bastian, Boris C. ;
Baylin, Stephen B. ;
Behera, Madhusmita ;
Belyaev, Dmitry ;
Benz, Christopher ;
Bernard, Brady ;
Beroukhim, Rameen ;
Bir, Natalie ;
Black, Aaron D. ;
Bodenheimer, Tom ;
Boice, Lori ;
Boland, Genevieve M. ;
Bono, Riccardo ;
Bootwalla, Moiz S. ;
Bosenberg, Marcus ;
Bowen, Jay ;
Bowlby, Reanne ;
Bristow, Christopher A. ;
Brockway-Lunardi, Laura ;
Brooks, Denise ;
Brzezinski, Jakub ;
Bshara, Wiam ;
Buda, Elizabeth ;
Burns, William R. ;
Butterfield, Yaron S. N. ;
Button, Michael ;
Calderone, Tiffany ;
Cappellini, Giancarlo Antonini ;
Carter, Candace ;
Carter, Scott L. ;
Cherney, Lynn ;
Cherniack, Andrew D. ;
Chevalier, Aaron ;
Chin, Lynda .
CELL, 2015, 161 (07) :1681-1696
[6]   Perturbations of the AKT signaling pathway in human cancer [J].
Altomare, DA ;
Testa, JR .
ONCOGENE, 2005, 24 (50) :7455-7464
[7]  
AMER MH, 1978, CANCER-AM CANCER SOC, V42, P660, DOI 10.1002/1097-0142(197808)42:2<660::AID-CNCR2820420237>3.0.CO
[8]  
2-E
[9]  
[Anonymous], 2013, CHEMOTHER RES PRACT
[10]  
[Anonymous], 2016, JPN J CLIN IMMUNOL, DOI DOI 10.2177/JSCI.39.51