Mechanisms, Diagnosis and Treatment of Bone Metastases

被引:61
作者
Ban, Jozef [1 ]
Fock, Valerie [1 ]
Aryee, Dave N. T. [1 ,2 ]
Kovar, Heinrich [1 ,2 ]
机构
[1] St Anna Childrens Canc Res Inst, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Pediat, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
bone metastasis; metastatic niche; tumor microenvironment interactions; bone colonization; EMT; metastatic dormancy; bone reconstruction; metastasis targeted therapy; PROSTATE-CANCER CELLS; HUMAN BREAST-CANCER; DISSEMINATED TUMOR-CELLS; OSTEOBLAST DIFFERENTIATION; EWINGS-SARCOMA; N-CADHERIN; OSTEOSARCOMA CELLS; TGF-BETA; IN-VIVO; MORPHOGENETIC PROTEIN-7;
D O I
10.3390/cells10112944
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bone and bone marrow are among the most frequent metastatic sites of cancer. The occurrence of bone metastasis is frequently associated with a dismal disease outcome. The prevention and therapy of bone metastases is a priority in the treatment of cancer patients. However, current therapeutic options for patients with bone metastatic disease are limited in efficacy and associated with increased morbidity. Therefore, most current therapies are mainly palliative in nature. A better understanding of the underlying molecular pathways of the bone metastatic process is warranted to develop novel, well-tolerated and more successful treatments for a significant improvement of patients' quality of life and disease outcome. In this review, we provide comparative mechanistic insights into the bone metastatic process of various solid tumors, including pediatric cancers. We also highlight current and innovative approaches to biologically targeted therapy and immunotherapy. In particular, we discuss the role of the bone marrow microenvironment in the attraction, homing, dormancy and outgrowth of metastatic tumor cells and the ensuing therapeutic implications. Multiple signaling pathways have been described to contribute to metastatic spread to the bone of specific cancer entities, with most knowledge derived from the study of breast and prostate cancer. However, it is likely that similar mechanisms are involved in different types of cancer, including multiple myeloma, primary bone sarcomas and neuroblastoma. The metastatic rate-limiting interaction of tumor cells with the various cellular and noncellular components of the bone-marrow niche provides attractive therapeutic targets, which are already partially exploited by novel promising immunotherapies.
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页数:30
相关论文
共 311 条
[1]   Vicious cycle between myeloma cell binding to bone marrow stromal cells via VLA-4-VCAM-1 adhesion and macrophage inflammatory protein-1α and MIP-1β production [J].
Abe, Masahiro ;
Hiura, Kenji ;
Ozaki, Shuji ;
Kido, Shinsuke ;
Matsumoto, Toshio .
JOURNAL OF BONE AND MINERAL METABOLISM, 2009, 27 (01) :16-23
[2]   STAG2 loss rewires oncogenic and developmental programs to promote metastasis in Ewing sarcoma [J].
Adane, Biniam ;
Alexe, Gabriela ;
Seong, Bo Kyung A. ;
Lu, Diana ;
Hwang, Elizabeth E. ;
Hnisz, Denes ;
Lareau, Caleb A. ;
Ross, Linda ;
Lin, Shan ;
Dela Cruz, Filemon S. ;
Richardson, Melissa ;
Weintraub, Abraham S. ;
Wang, Sarah ;
Iniguez, Amanda Balboni ;
Dharia, Neekesh, V ;
Conway, Amy Saur ;
Robichaud, Amanda L. ;
Tanenbaum, Benjamin ;
Krill-Burger, John M. ;
Vazquez, Francisca ;
Schenone, Monica ;
Berman, Jason N. ;
Kung, Andrew L. ;
Carr, Steven A. ;
Aryee, Martin J. ;
Young, Richard A. ;
Crompton, Brian D. ;
Stegmaier, Kimberly .
CANCER CELL, 2021, 39 (06) :827-+
[3]   CXCR5 may be involved in the attraction of human metastatic neuroblastoma cells to the bone marrow [J].
Airoldi, Irma ;
Cocco, Claudia ;
Morandi, Fabio ;
Prigione, Ignazia ;
Pistoia, Vito .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2008, 57 (04) :541-548
[4]   N-MYC DOWN REGULATES NEURAL CELL-ADHESION MOLECULE EXPRESSION IN RAT NEUROBLASTOMA [J].
AKESON, R ;
BERNARDS, R .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (05) :2012-2016
[5]   N-cadherin gene expression in prostate carcinoma is modulated by integrin-dependent nuclear translocation of Twist1 [J].
Alexander, NR ;
Tran, NL ;
Rekapally, H ;
Summers, CE ;
Glackin, C ;
Heimark, RL .
CANCER RESEARCH, 2006, 66 (07) :3365-3369
[6]   Capecitabine Monotherapy is Efficient and Safe in All Line Settings in Patients with Metastatic and Advanced Breast Cancer [J].
Amari, Masakazu ;
Ishida, Takanori ;
Takeda, Motohiro ;
Ohuchi, Noriaki .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 40 (03) :188-193
[7]   Combination and sequential treatment in women with postmenopausal osteoporosis [J].
Anastasilakis, Athanasios D. ;
Polyzos, Stergios A. ;
Yavropoulou, Maria P. ;
Makras, Polyzois .
EXPERT OPINION ON PHARMACOTHERAPY, 2020, 21 (04) :477-490
[8]   Metastatic fractures of long limb bones [J].
Anract, P. ;
Biau, D. ;
Boudou-Rouquette, P. .
ORTHOPAEDICS & TRAUMATOLOGY-SURGERY & RESEARCH, 2017, 103 (01) :S41-S51
[9]   Targeting Macrophages: Friends or Foes in Disease? [J].
Ardura, Juan A. ;
Rackov, Gorjana ;
Izquierdo, Elena ;
Alonso, Veronica ;
Gortazar, Arancha R. ;
Escribese, Maria M. .
FRONTIERS IN PHARMACOLOGY, 2019, 10
[10]   Quantitative Assessment of Bone Metastasis in Prostate Cancer Using Synthetic Magnetic Resonance Imaging [J].
Arita, Yuki ;
Takahara, Taro ;
Yoshida, Soichiro ;
Kwee, Thomas C. ;
Yajima, Shugo ;
Ishii, Chikako ;
Ishii, Ryota ;
Okuda, Shigeo ;
Jinzaki, Masahiro ;
Fujii, Yasuhisa .
INVESTIGATIVE RADIOLOGY, 2019, 54 (10) :638-644