Skip to main content
Erschienen in: Current Osteoporosis Reports 4/2017

08.06.2017 | Cancer-induced Musculoskeletal Diseases (M Reagan and E Keller, Section Editors)

Hypoxia and Bone Metastatic Disease

verfasst von: Rachelle W. Johnson, Miranda E. Sowder, Amato J. Giaccia

Erschienen in: Current Osteoporosis Reports | Ausgabe 4/2017

Einloggen, um Zugang zu erhalten

Abstract

Purpose of Review

This review highlights our current knowledge of oxygen tensions in the bone marrow, and how low oxygen tensions (hypoxia) regulate tumor metastasis to and colonization of the bone marrow.

Recent Findings

The bone marrow is a relatively hypoxic microenvironment, but oxygen tensions fluctuate throughout the marrow cavity and across the endosteal and periosteal surfaces. Recent advances in imaging have made it possible to better characterize these fluctuations in bone oxygenation, but technical challenges remain. We have compiled evidence from multiple groups that suggests that hypoxia or hypoxia inducible factor (HIF) signaling may induce spontaneous metastasis to the bone and promote tumor colonization of bone, particularly in the case of breast cancer dissemination to the bone marrow.

Summary

We are beginning to understand oxygenation patterns within the bone compartment and the role for hypoxia and HIF signaling in tumor cell dissemination to the bone marrow, but further studies are warranted.
Literatur
1.
Zurück zum Zitat Brown JM, Giaccia AJ. The unique physiology of solid tumors: opportunities (and problems) for cancer therapy. Cancer res. 1998;58(7):1408–16.PubMed Brown JM, Giaccia AJ. The unique physiology of solid tumors: opportunities (and problems) for cancer therapy. Cancer res. 1998;58(7):1408–16.PubMed
2.
Zurück zum Zitat Schindl M, Schoppmann SF, Samonigg H, Hausmaninger H, Kwasny W, Gnant M, et al. Overexpression of hypoxia-inducible factor 1alpha is associated with an unfavorable prognosis in lymph node-positive breast cancer. Clinical Cancer Research: an Official Journal of the American Association for Cancer Research. 2002;8(6):1831–7. Schindl M, Schoppmann SF, Samonigg H, Hausmaninger H, Kwasny W, Gnant M, et al. Overexpression of hypoxia-inducible factor 1alpha is associated with an unfavorable prognosis in lymph node-positive breast cancer. Clinical Cancer Research: an Official Journal of the American Association for Cancer Research. 2002;8(6):1831–7.
3.
Zurück zum Zitat Bos R, van der Groep P, Greijer AE, Shvarts A, Meijer S, Pinedo HM, et al. Levels of hypoxia-inducible factor-1alpha independently predict prognosis in patients with lymph node negative breast carcinoma. Cancer. 2003;97(6):1573–81. doi:10.1002/cncr.11246.CrossRefPubMed Bos R, van der Groep P, Greijer AE, Shvarts A, Meijer S, Pinedo HM, et al. Levels of hypoxia-inducible factor-1alpha independently predict prognosis in patients with lymph node negative breast carcinoma. Cancer. 2003;97(6):1573–81. doi:10.​1002/​cncr.​11246.CrossRefPubMed
4.
Zurück zum Zitat Dales JP, Garcia S, Meunier-Carpentier S, Andrac-Meyer L, Haddad O, Lavaut MN, et al. Overexpression of hypoxia-inducible factor HIF-1alpha predicts early relapse in breast cancer: retrospective study in a series of 745 patients. International Journal of Cancer Journal International du Cancer. 2005;116(5):734–9. doi:10.1002/ijc.20984.CrossRefPubMed Dales JP, Garcia S, Meunier-Carpentier S, Andrac-Meyer L, Haddad O, Lavaut MN, et al. Overexpression of hypoxia-inducible factor HIF-1alpha predicts early relapse in breast cancer: retrospective study in a series of 745 patients. International Journal of Cancer Journal International du Cancer. 2005;116(5):734–9. doi:10.​1002/​ijc.​20984.CrossRefPubMed
5.
Zurück zum Zitat Generali D, Berruti A, Brizzi MP, Campo L, Bonardi S, Wigfield S, et al. Hypoxia-inducible factor-1alpha expression predicts a poor response to primary chemoendocrine therapy and disease-free survival in primary human breast cancer. Clinical Cancer Research : an Official Journal of the American Association for Cancer Research. 2006;12(15):4562–8. doi:10.1158/1078-0432.CCR-05-2690.CrossRef Generali D, Berruti A, Brizzi MP, Campo L, Bonardi S, Wigfield S, et al. Hypoxia-inducible factor-1alpha expression predicts a poor response to primary chemoendocrine therapy and disease-free survival in primary human breast cancer. Clinical Cancer Research : an Official Journal of the American Association for Cancer Research. 2006;12(15):4562–8. doi:10.​1158/​1078-0432.​CCR-05-2690.CrossRef
6.
Zurück zum Zitat Yamamoto Y, Ibusuki M, Okumura Y, Kawasoe T, Kai K, Iyama K, et al. Hypoxia-inducible factor 1alpha is closely linked to an aggressive phenotype in breast cancer. Breast Cancer res Treat. 2008;110(3):465–75. doi:10.1007/s10549-007-9742-1.CrossRefPubMed Yamamoto Y, Ibusuki M, Okumura Y, Kawasoe T, Kai K, Iyama K, et al. Hypoxia-inducible factor 1alpha is closely linked to an aggressive phenotype in breast cancer. Breast Cancer res Treat. 2008;110(3):465–75. doi:10.​1007/​s10549-007-9742-1.CrossRefPubMed
8.
Zurück zum Zitat Matsuo Y, Ding Q, Desaki R, Maemura K, Mataki Y, Shinchi H, et al. Hypoxia inducible factor-1 alpha plays a pivotal role in hepatic metastasis of pancreatic cancer: an immunohistochemical study. J Hepatobiliary Pancreat Sci. 2014;21(2):105–12. doi:10.1002/jhbp.6.CrossRefPubMed Matsuo Y, Ding Q, Desaki R, Maemura K, Mataki Y, Shinchi H, et al. Hypoxia inducible factor-1 alpha plays a pivotal role in hepatic metastasis of pancreatic cancer: an immunohistochemical study. J Hepatobiliary Pancreat Sci. 2014;21(2):105–12. doi:10.​1002/​jhbp.​6.CrossRefPubMed
9.
Zurück zum Zitat Ping W, Sun W, Zu Y, Chen W, Fu X. Clinicopathological and prognostic significance of hypoxia-inducible factor-1alpha in esophageal squamous cell carcinoma: a meta-analysis. Tumour Biol. 2014;35(5):4401–9. doi:10.1007/s13277-013-1579-0.CrossRefPubMed Ping W, Sun W, Zu Y, Chen W, Fu X. Clinicopathological and prognostic significance of hypoxia-inducible factor-1alpha in esophageal squamous cell carcinoma: a meta-analysis. Tumour Biol. 2014;35(5):4401–9. doi:10.​1007/​s13277-013-1579-0.CrossRefPubMed
13.
Zurück zum Zitat Epstein AC, Gleadle JM, McNeill LA, Hewitson KS, O'Rourke J, Mole DR, et al. C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell. 2001;107(1):43–54.CrossRefPubMed Epstein AC, Gleadle JM, McNeill LA, Hewitson KS, O'Rourke J, Mole DR, et al. C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell. 2001;107(1):43–54.CrossRefPubMed
15.
Zurück zum Zitat Ivan M, Haberberger T, Gervasi DC, Michelson KS, Gunzler V, Kondo K, et al. Biochemical purification and pharmacological inhibition of a mammalian prolyl hydroxylase acting on hypoxia-inducible factor. Proc Natl Acad Sci U S a. 2002;99(21):13459–64. doi:10.1073/pnas.192342099.CrossRefPubMedPubMedCentral Ivan M, Haberberger T, Gervasi DC, Michelson KS, Gunzler V, Kondo K, et al. Biochemical purification and pharmacological inhibition of a mammalian prolyl hydroxylase acting on hypoxia-inducible factor. Proc Natl Acad Sci U S a. 2002;99(21):13459–64. doi:10.​1073/​pnas.​192342099.CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Maxwell PH, Wiesener MS, Chang GW, Clifford SC, Vaux EC, Cockman ME, et al. The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. Nature. 1999;399(6733):271–5. doi:10.1038/20459.CrossRefPubMed Maxwell PH, Wiesener MS, Chang GW, Clifford SC, Vaux EC, Cockman ME, et al. The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. Nature. 1999;399(6733):271–5. doi:10.​1038/​20459.CrossRefPubMed
18.
Zurück zum Zitat Jaakkola P, Mole DR, Tian YM, Wilson MI, Gielbert J, Gaskell SJ, et al. Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. Science. 2001;292(5516):468–72. doi:10.1126/science.1059796.CrossRefPubMed Jaakkola P, Mole DR, Tian YM, Wilson MI, Gielbert J, Gaskell SJ, et al. Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. Science. 2001;292(5516):468–72. doi:10.​1126/​science.​1059796.CrossRefPubMed
19.
20.
Zurück zum Zitat Maynard MA, Qi H, Chung J, Lee EH, Kondo Y, Hara S, et al. Multiple splice variants of the human HIF-3 alpha locus are targets of the von Hippel-Lindau E3 ubiquitin ligase complex. J Biol Chem. 2003;278(13):11032–40. doi:10.1074/jbc.M208681200.CrossRefPubMed Maynard MA, Qi H, Chung J, Lee EH, Kondo Y, Hara S, et al. Multiple splice variants of the human HIF-3 alpha locus are targets of the von Hippel-Lindau E3 ubiquitin ligase complex. J Biol Chem. 2003;278(13):11032–40. doi:10.​1074/​jbc.​M208681200.CrossRefPubMed
22.
Zurück zum Zitat Wang GL, Semenza GL. General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia. Proc Natl Acad Sci U S a. 1993;90(9):4304–8.CrossRefPubMedPubMedCentral Wang GL, Semenza GL. General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia. Proc Natl Acad Sci U S a. 1993;90(9):4304–8.CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat Wang GL, Jiang BH, Rue EA, Semenza GL. Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. Proc Natl Acad Sci U S a. 1995;92(12):5510–4.CrossRefPubMedPubMedCentral Wang GL, Jiang BH, Rue EA, Semenza GL. Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. Proc Natl Acad Sci U S a. 1995;92(12):5510–4.CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Xiong J, O'Brien CA. Osteocyte RANKL: new insights into the control of bone remodeling. Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research. 2012;27(3):499–505. doi:10.1002/jbmr.1547.CrossRef Xiong J, O'Brien CA. Osteocyte RANKL: new insights into the control of bone remodeling. Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research. 2012;27(3):499–505. doi:10.​1002/​jbmr.​1547.CrossRef
28.
Zurück zum Zitat • Croucher PI, McDonald MM, Martin TJ. Bone metastasis: the importance of the neighbourhood. Nat rev Cancer. 2016;16(6):373–86. doi:10.1038/nrc.2016.44. A nice recent review of tumor metastasis and dormancy in the bone marrow. CrossRefPubMed • Croucher PI, McDonald MM, Martin TJ. Bone metastasis: the importance of the neighbourhood. Nat rev Cancer. 2016;16(6):373–86. doi:10.​1038/​nrc.​2016.​44. A nice recent review of tumor metastasis and dormancy in the bone marrow. CrossRefPubMed
30.
Zurück zum Zitat •• Spencer JA, Ferraro F, Roussakis E, Klein A, Wu J, Runnels JM, et al. Direct measurement of local oxygen concentration in the bone marrow of live animals. Nature. 2014;508(7495):269–73. doi:10.1038/nature13034. Showed quantitatively for the first time differences in oxygen tensions within different regions of the calvaria. CrossRefPubMedPubMedCentral •• Spencer JA, Ferraro F, Roussakis E, Klein A, Wu J, Runnels JM, et al. Direct measurement of local oxygen concentration in the bone marrow of live animals. Nature. 2014;508(7495):269–73. doi:10.​1038/​nature13034. Showed quantitatively for the first time differences in oxygen tensions within different regions of the calvaria. CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Chow DC, Wenning LA, Miller WM, Papoutsakis ET. Modeling pO2 distributions in the bone marrow hematopoietic compartment. I. Krogh’s model. Biophys J. 2001;81(2):675–84.CrossRefPubMedPubMedCentral Chow DC, Wenning LA, Miller WM, Papoutsakis ET. Modeling pO2 distributions in the bone marrow hematopoietic compartment. I. Krogh’s model. Biophys J. 2001;81(2):675–84.CrossRefPubMedPubMedCentral
32.
Zurück zum Zitat Harrison JS, Rameshwar P, Chang V, Bandari P. Oxygen saturation in the bone marrow of healthy volunteers. Blood. 2002;99(1):394.CrossRefPubMed Harrison JS, Rameshwar P, Chang V, Bandari P. Oxygen saturation in the bone marrow of healthy volunteers. Blood. 2002;99(1):394.CrossRefPubMed
34.
Zurück zum Zitat Branemark P-I. Experimental investigation of microcirculation in bone marrow. Angiology. 1961;12(7):293–305.CrossRef Branemark P-I. Experimental investigation of microcirculation in bone marrow. Angiology. 1961;12(7):293–305.CrossRef
35.
Zurück zum Zitat • Kusumbe AP, Ramasamy SK, Adams RH. Coupling of angiogenesis and osteogenesis by a specific vessel subtype in bone. Nature. 2014;507(7492):323–8. doi:10.1038/nature13145. Identified different vessel types in the bone, which link angiogenesis and osteogenesis, and show that these blood vessels decline with age. CrossRefPubMedPubMedCentral • Kusumbe AP, Ramasamy SK, Adams RH. Coupling of angiogenesis and osteogenesis by a specific vessel subtype in bone. Nature. 2014;507(7492):323–8. doi:10.​1038/​nature13145. Identified different vessel types in the bone, which link angiogenesis and osteogenesis, and show that these blood vessels decline with age. CrossRefPubMedPubMedCentral
41.
Zurück zum Zitat Nombela-Arrieta C, Pivarnik G, Winkel B, Canty KJ, Harley B, Mahoney JE, et al. Quantitative imaging of haematopoietic stem and progenitor cell localization and hypoxic status in the bone marrow microenvironment. Nat Cell Biol. 2013;15(5):533–43. doi:10.1038/ncb2730.CrossRefPubMedPubMedCentral Nombela-Arrieta C, Pivarnik G, Winkel B, Canty KJ, Harley B, Mahoney JE, et al. Quantitative imaging of haematopoietic stem and progenitor cell localization and hypoxic status in the bone marrow microenvironment. Nat Cell Biol. 2013;15(5):533–43. doi:10.​1038/​ncb2730.CrossRefPubMedPubMedCentral
42.
Zurück zum Zitat Winkler IG, Barbier V, Wadley R, Zannettino AC, Williams S, Levesque JP. Positioning of bone marrow hematopoietic and stromal cells relative to blood flow in vivo: serially reconstituting hematopoietic stem cells reside in distinct nonperfused niches. Blood. 2010;116(3):375–85. doi:10.1182/blood-2009-07-233437.CrossRefPubMed Winkler IG, Barbier V, Wadley R, Zannettino AC, Williams S, Levesque JP. Positioning of bone marrow hematopoietic and stromal cells relative to blood flow in vivo: serially reconstituting hematopoietic stem cells reside in distinct nonperfused niches. Blood. 2010;116(3):375–85. doi:10.​1182/​blood-2009-07-233437.CrossRefPubMed
43.
Zurück zum Zitat Lassailly F, Foster K, Lopez-Onieva L, Currie E, Bonnet D. Multimodal imaging reveals structural and functional heterogeneity in different bone marrow compartments: functional implications on hematopoietic stem cells. Blood. 2013;122(10):1730–40. doi:10.1182/blood-2012-11-467498.CrossRefPubMed Lassailly F, Foster K, Lopez-Onieva L, Currie E, Bonnet D. Multimodal imaging reveals structural and functional heterogeneity in different bone marrow compartments: functional implications on hematopoietic stem cells. Blood. 2013;122(10):1730–40. doi:10.​1182/​blood-2012-11-467498.CrossRefPubMed
44.
46.
Zurück zum Zitat Lo Celso C, Fleming HE, Wu JW, Zhao CX, Miake-Lye S, Fujisaki J, et al. Live-animal tracking of individual haematopoietic stem/progenitor cells in their niche. Nature. 2009;457(7225):92–6. doi:10.1038/nature07434.CrossRefPubMed Lo Celso C, Fleming HE, Wu JW, Zhao CX, Miake-Lye S, Fujisaki J, et al. Live-animal tracking of individual haematopoietic stem/progenitor cells in their niche. Nature. 2009;457(7225):92–6. doi:10.​1038/​nature07434.CrossRefPubMed
48.
49.
Zurück zum Zitat Finger EC, Castellini L, Rankin EB, Vilalta M, Krieg AJ, Jiang D, et al. Hypoxic induction of AKAP12 variant 2 shifts PKA-mediated protein phosphorylation to enhance migration and metastasis of melanoma cells. Proc Natl Acad Sci U S A. 2015;112(14):4441–6. doi:10.1073/pnas.1418164112.CrossRefPubMedPubMedCentral Finger EC, Castellini L, Rankin EB, Vilalta M, Krieg AJ, Jiang D, et al. Hypoxic induction of AKAP12 variant 2 shifts PKA-mediated protein phosphorylation to enhance migration and metastasis of melanoma cells. Proc Natl Acad Sci U S A. 2015;112(14):4441–6. doi:10.​1073/​pnas.​1418164112.CrossRefPubMedPubMedCentral
51.
Zurück zum Zitat Chaturvedi P, Gilkes DM, Wong CC, Kshitiz LW, Zhang H, et al. Hypoxia-inducible factor-dependent breast cancer-mesenchymal stem cell bidirectional signaling promotes metastasis. J Clin Invest. 2013;123(1):189–205. doi:10.1172/JCI64993.CrossRefPubMed Chaturvedi P, Gilkes DM, Wong CC, Kshitiz LW, Zhang H, et al. Hypoxia-inducible factor-dependent breast cancer-mesenchymal stem cell bidirectional signaling promotes metastasis. J Clin Invest. 2013;123(1):189–205. doi:10.​1172/​JCI64993.CrossRefPubMed
52.
Zurück zum Zitat Woelfle U, Cloos J, Sauter G, Riethdorf L, Janicke F, van Diest P, et al. Molecular signature associated with bone marrow micrometastasis in human breast cancer. Cancer res. 2003;63(18):5679–84.PubMed Woelfle U, Cloos J, Sauter G, Riethdorf L, Janicke F, van Diest P, et al. Molecular signature associated with bone marrow micrometastasis in human breast cancer. Cancer res. 2003;63(18):5679–84.PubMed
61.
Zurück zum Zitat Graham CH, Forsdike J, Fitzgerald CJ, Macdonald-Goodfellow S. Hypoxia-mediated stimulation of carcinoma cell invasiveness via upregulation of urokinase receptor expression. International Journal of Cancer Journal International du Cancer. 1999;80(4):617–23.CrossRefPubMed Graham CH, Forsdike J, Fitzgerald CJ, Macdonald-Goodfellow S. Hypoxia-mediated stimulation of carcinoma cell invasiveness via upregulation of urokinase receptor expression. International Journal of Cancer Journal International du Cancer. 1999;80(4):617–23.CrossRefPubMed
62.
Zurück zum Zitat Buchler P, Reber HA, Tomlinson JS, Hankinson O, Kallifatidis G, Friess H, et al. Transcriptional regulation of urokinase-type plasminogen activator receptor by hypoxia-inducible factor 1 is crucial for invasion of pancreatic and liver cancer. Neoplasia. 2009;11(2):196–206.CrossRefPubMedPubMedCentral Buchler P, Reber HA, Tomlinson JS, Hankinson O, Kallifatidis G, Friess H, et al. Transcriptional regulation of urokinase-type plasminogen activator receptor by hypoxia-inducible factor 1 is crucial for invasion of pancreatic and liver cancer. Neoplasia. 2009;11(2):196–206.CrossRefPubMedPubMedCentral
63.
Zurück zum Zitat Allgayer H, Heiss MM, Riesenberg R, Grutzner KU, Tarabichi A, Babic R, et al. Urokinase plasminogen activator receptor (uPA-R): one potential characteristic of metastatic phenotypes in minimal residual tumor disease. Cancer res. 1997;57(7):1394–9.PubMed Allgayer H, Heiss MM, Riesenberg R, Grutzner KU, Tarabichi A, Babic R, et al. Urokinase plasminogen activator receptor (uPA-R): one potential characteristic of metastatic phenotypes in minimal residual tumor disease. Cancer res. 1997;57(7):1394–9.PubMed
64.
Zurück zum Zitat Heiss MM, Allgayer H, Gruetzner KU, Funke I, Babic R, Jauch KW, et al. Individual development and uPA-receptor expression of disseminated tumour cells in bone marrow: a reference to early systemic disease in solid cancer. Nat med. 1995;1(10):1035–9.CrossRefPubMed Heiss MM, Allgayer H, Gruetzner KU, Funke I, Babic R, Jauch KW, et al. Individual development and uPA-receptor expression of disseminated tumour cells in bone marrow: a reference to early systemic disease in solid cancer. Nat med. 1995;1(10):1035–9.CrossRefPubMed
65.
Zurück zum Zitat Allgayer H, Heiss MM, Riesenberg R, Babic R, Jauch KW, Schildberg FW. Immunocytochemical phenotyping of disseminated tumor cells in bone marrow by uPA receptor and CK18: investigation of sensitivity and specificity of an immunogold/alkaline phosphatase double staining protocol. J Histochem Cytochem. 1997;45(2):203–12.CrossRefPubMed Allgayer H, Heiss MM, Riesenberg R, Babic R, Jauch KW, Schildberg FW. Immunocytochemical phenotyping of disseminated tumor cells in bone marrow by uPA receptor and CK18: investigation of sensitivity and specificity of an immunogold/alkaline phosphatase double staining protocol. J Histochem Cytochem. 1997;45(2):203–12.CrossRefPubMed
67.
Zurück zum Zitat Yu W, Kim J, Ossowski L. Reduction in surface urokinase receptor forces malignant cells into a protracted state of dormancy. J Cell Biol. 1997;137(3):767–77.CrossRefPubMedPubMedCentral Yu W, Kim J, Ossowski L. Reduction in surface urokinase receptor forces malignant cells into a protracted state of dormancy. J Cell Biol. 1997;137(3):767–77.CrossRefPubMedPubMedCentral
68.
Zurück zum Zitat • Johnson RW, Finger EC, Olcina MM, Vilalta M, Aguilera T, Miao Y, et al. Induction of LIFR confers a dormancy phenotype in breast cancer cells disseminated to the bone marrow. Nat Cell Biol. 2016;18(10):1078–89. doi:10.1038/ncb3408. Identified a hypoxia-dependent role for LIFR in breast cancer dormancy in the bone marrow. CrossRefPubMedPubMedCentral • Johnson RW, Finger EC, Olcina MM, Vilalta M, Aguilera T, Miao Y, et al. Induction of LIFR confers a dormancy phenotype in breast cancer cells disseminated to the bone marrow. Nat Cell Biol. 2016;18(10):1078–89. doi:10.​1038/​ncb3408. Identified a hypoxia-dependent role for LIFR in breast cancer dormancy in the bone marrow. CrossRefPubMedPubMedCentral
69.
Zurück zum Zitat Bromberg JF, Wrzeszczynska MH, Devgan G, Zhao Y, Pestell RG, Albanese C, et al. Stat3 as an oncogene. Cell. 1999;98(3):295–303.CrossRefPubMed Bromberg JF, Wrzeszczynska MH, Devgan G, Zhao Y, Pestell RG, Albanese C, et al. Stat3 as an oncogene. Cell. 1999;98(3):295–303.CrossRefPubMed
70.
Zurück zum Zitat Bromberg JF, Horvath CM, Besser D, Lathem WW, Darnell JE Jr. Stat3 activation is required for cellular transformation by v-src. Mol Cell Biol. 1998;18(5):2553–8.CrossRefPubMedPubMedCentral Bromberg JF, Horvath CM, Besser D, Lathem WW, Darnell JE Jr. Stat3 activation is required for cellular transformation by v-src. Mol Cell Biol. 1998;18(5):2553–8.CrossRefPubMedPubMedCentral
71.
Zurück zum Zitat Watson CJ, Miller WR. Elevated levels of members of the STAT family of transcription factors in breast carcinoma nuclear extracts. Br J Cancer. 1995;71(4):840–4.CrossRefPubMedPubMedCentral Watson CJ, Miller WR. Elevated levels of members of the STAT family of transcription factors in breast carcinoma nuclear extracts. Br J Cancer. 1995;71(4):840–4.CrossRefPubMedPubMedCentral
72.
Zurück zum Zitat Garcia R, Bowman TL, Niu G, Yu H, Minton S, Muro-Cacho CA, et al. Constitutive activation of Stat3 by the Src and JAK tyrosine kinases participates in growth regulation of human breast carcinoma cells. Oncogene. 2001;20(20):2499–513. doi:10.1038/sj.onc.1204349.CrossRefPubMed Garcia R, Bowman TL, Niu G, Yu H, Minton S, Muro-Cacho CA, et al. Constitutive activation of Stat3 by the Src and JAK tyrosine kinases participates in growth regulation of human breast carcinoma cells. Oncogene. 2001;20(20):2499–513. doi:10.​1038/​sj.​onc.​1204349.CrossRefPubMed
75.
Zurück zum Zitat • Fluegen G, Avivar-Valderas A, Wang Y, Padgen MR, Williams JK, Nobre AR, et al. Phenotypic heterogeneity of disseminated tumour cells is preset by primary tumour hypoxic microenvironments. Nat Cell Biol. 2017;19(2):120–32. doi:10.1038/ncb3465. Found that tumor hypoxia creates a distinct population of DTCs that are resistant to chemotherapy and may give rise to distant metastases. CrossRefPubMedPubMedCentral • Fluegen G, Avivar-Valderas A, Wang Y, Padgen MR, Williams JK, Nobre AR, et al. Phenotypic heterogeneity of disseminated tumour cells is preset by primary tumour hypoxic microenvironments. Nat Cell Biol. 2017;19(2):120–32. doi:10.​1038/​ncb3465. Found that tumor hypoxia creates a distinct population of DTCs that are resistant to chemotherapy and may give rise to distant metastases. CrossRefPubMedPubMedCentral
76.
Zurück zum Zitat Sosa MS, Parikh F, Maia AG, Estrada Y, Bosch A, Bragado P, et al. NR2F1 controls tumour cell dormancy via SOX9- and RARbeta-driven quiescence programmes. Nat Commun. 2015;6:6170. doi:10.1038/ncomms7170.CrossRefPubMed Sosa MS, Parikh F, Maia AG, Estrada Y, Bosch A, Bragado P, et al. NR2F1 controls tumour cell dormancy via SOX9- and RARbeta-driven quiescence programmes. Nat Commun. 2015;6:6170. doi:10.​1038/​ncomms7170.CrossRefPubMed
79.
Zurück zum Zitat Bragado P, Estrada Y, Parikh F, Krause S, Capobianco C, Farina HG, et al. TGF-beta2 dictates disseminated tumour cell fate in target organs through TGF-beta-RIII and p38alpha/beta signalling. Nat Cell Biol. 2013;15(11):1351–61. doi:10.1038/ncb2861.CrossRefPubMedPubMedCentral Bragado P, Estrada Y, Parikh F, Krause S, Capobianco C, Farina HG, et al. TGF-beta2 dictates disseminated tumour cell fate in target organs through TGF-beta-RIII and p38alpha/beta signalling. Nat Cell Biol. 2013;15(11):1351–61. doi:10.​1038/​ncb2861.CrossRefPubMedPubMedCentral
Metadaten
Titel
Hypoxia and Bone Metastatic Disease
verfasst von
Rachelle W. Johnson
Miranda E. Sowder
Amato J. Giaccia
Publikationsdatum
08.06.2017
Verlag
Springer US
Erschienen in
Current Osteoporosis Reports / Ausgabe 4/2017
Print ISSN: 1544-1873
Elektronische ISSN: 1544-2241
DOI
https://doi.org/10.1007/s11914-017-0378-8

Weitere Artikel der Ausgabe 4/2017

Current Osteoporosis Reports 4/2017 Zur Ausgabe

Osteoimmunology (MB Humphrey and M Nakamura, Section Editors)

Osteomacs and Bone Regeneration

Pediatrics (L Ward and E Imel, Section Editors)

Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility

Skeletal Development (P Trainor and K Svoboda, Section Editors)

microRNA Regulation of Skeletal Development

Arthropedia

Grundlagenwissen der Arthroskopie und Gelenkchirurgie. Erweitert durch Fallbeispiele, Videos und Abbildungen. 
» Jetzt entdecken

Update Orthopädie und Unfallchirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.