Bone metastasis and the metastatic niche

Verfasser / Beitragende:
[Guangwen Ren, Mark Esposito, Yibin Kang]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Medicine, 93/11(2015-11-01), 1203-1212
Format:
Artikel (online)
ID: 605544077
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024 7 0 |a 10.1007/s00109-015-1329-4  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00109-015-1329-4 
245 0 0 |a Bone metastasis and the metastatic niche  |h [Elektronische Daten]  |c [Guangwen Ren, Mark Esposito, Yibin Kang] 
520 3 |a The bone marrow has been long known to host a unique environment amenable to colonization by metastasizing tumor cells. Yet, the underlying molecular interactions within this specialized microenvironment which give rise to the high incidence of bone metastasis in breast and prostate cancer patients have long remained uncharacterized. With the recent description of the bone metastatic "niche,” considerable focus has been placed on understanding how the bone stroma contributes to each step of metastasis. Discoveries within this field have demonstrated that when cancer cells home to the niche in which hematopoietic and mesenchymal stem/progenitor cells normally reside, a bidirectional crosstalk emerges between the tumor cells and the bone metastatic stroma. This communication modulates every step of cancer cell metastasis to the bone, including the initial homing and seeding, formation of micrometastases, outgrowth of macrometastases, and the maintenance of long-term dormancy of disseminated tumor cells in the bone. In clinical practice, targeting the bone metastatic niche is evolving into a promising avenue for the prevention of bone metastatic relapse, therapeutic resistance, and other aspects of cancer progression. Here, we review the current knowledge concerning the role of the bone metastatic niche in bone metastasis. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Bone metastasis  |2 nationallicence 
690 7 |a Metastatic niche  |2 nationallicence 
690 7 |a Osteoblastic niche  |2 nationallicence 
690 7 |a Perivascular niche  |2 nationallicence 
690 7 |a Tumor dormancy  |2 nationallicence 
690 7 |a Hematopoiesis  |2 nationallicence 
700 1 |a Ren  |D Guangwen  |u Department of Molecular Biology, Princeton University, LTL255, Washington Road, 08544, Princeton, NJ, USA  |4 aut 
700 1 |a Esposito  |D Mark  |u Department of Molecular Biology, Princeton University, LTL255, Washington Road, 08544, Princeton, NJ, USA  |4 aut 
700 1 |a Kang  |D Yibin  |u Department of Molecular Biology, Princeton University, LTL255, Washington Road, 08544, Princeton, NJ, USA  |4 aut 
773 0 |t Journal of Molecular Medicine  |d Springer Berlin Heidelberg  |g 93/11(2015-11-01), 1203-1212  |x 0946-2716  |q 93:11<1203  |1 2015  |2 93  |o 109 
856 4 0 |u https://doi.org/10.1007/s00109-015-1329-4  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a review-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00109-015-1329-4  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ren  |D Guangwen  |u Department of Molecular Biology, Princeton University, LTL255, Washington Road, 08544, Princeton, NJ, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Esposito  |D Mark  |u Department of Molecular Biology, Princeton University, LTL255, Washington Road, 08544, Princeton, NJ, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kang  |D Yibin  |u Department of Molecular Biology, Princeton University, LTL255, Washington Road, 08544, Princeton, NJ, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Molecular Medicine  |d Springer Berlin Heidelberg  |g 93/11(2015-11-01), 1203-1212  |x 0946-2716  |q 93:11<1203  |1 2015  |2 93  |o 109