Changes in the peripheral blood and bone marrow from untreated advanced breast cancer patients that are associated with the establishment of bone metastases
Bone metastasis is an incurable complication of breast cancer affecting 70-80 % of advanced patients. It is a multistep process that includes tumour cell mobilisation, intravasation, survival in the circulation, extravasation, migration and proliferation in the bone marrow/bone. Although novel findi...
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| Otros Autores: | , , , , , , , , , |
| Formato: | Capítulo de libro |
| Lenguaje: | Inglés |
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2014
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| Acceso en línea: | Registro en Scopus DOI Handle Registro en la Biblioteca Digital |
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| LEADER | 31629caa a22016817a 4500 | ||
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| 001 | PAPER-23888 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518205539.0 | ||
| 008 | 190411s2014 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-84895071039 | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a CEXMD | ||
| 100 | 1 | |a Martinez, L.M. | |
| 245 | 1 | 0 | |a Changes in the peripheral blood and bone marrow from untreated advanced breast cancer patients that are associated with the establishment of bone metastases |
| 260 | |c 2014 | ||
| 270 | 1 | 0 | |m Chasseing, N.A.; Immunohematology Laboratory, Experimental Biology and Medicine Institute (IBYME), National Council of Scientific and Technical Research (CONICET), 2490 Vuelta de Obligado, 1428 Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina; email: achasseing@ibyme.conicet.gov.ar |
| 506 | |2 openaire |e Política editorial | ||
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| 520 | 3 | |a Bone metastasis is an incurable complication of breast cancer affecting 70-80 % of advanced patients. It is a multistep process that includes tumour cell mobilisation, intravasation, survival in the circulation, extravasation, migration and proliferation in the bone marrow/bone. Although novel findings demonstrate the bone marrow microenvironment significance in bone metastatic progression, a majority of studies have focused on end-stage disease and little is known about how the pre-metastatic niche arises in the bone marrow/bone tissues. We demonstrated a significant increase in patients' peripheral blood plasma ability to induce transendothelial migration of MCF-7 cells compared with healthy volunteers. Moreover, high RANKL, MIF and OPG levels in patients' peripheral blood could play a role in the intravasation, angiogenesis, survival and epithelial-mesenchymal transition of circulating tumour cells. Also, we observed a significant increase in patients' bone marrow plasma capacity to induce transendothelial migration of MDA-MB231 and MCF-7 cells compared with healthy volunteers. Furthermore, patients' bone marrow mesenchymal stem cells could control the recruitment of tumour cells, modifying the MCF-7 and MDA-MB231 cell migration. In addition, we found a significantly higher MDA-MB231 cell proliferation when we used patients' bone marrow plasma compared with healthy volunteers. Interestingly, PDGF-AB, ICAM-1 and VCAM-1 levels in patients' bone marrow were significantly higher than the values of healthy volunteers, suggesting that they could be involved in the cancer cell extravasation, bone resorption and cancer cell proliferation. We believe that these results can reveal new information about what alterations happen in the bone marrow of advanced breast cancer patients before bone colonisation, changes that create optimal soil for the metastatic cascade progression. © 2013 Springer Science+Business Media Dordrecht. |l eng | |
| 536 | |a Detalles de la financiación: National Council for Scientific Research | ||
| 536 | |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas, PICT2006 | ||
| 536 | |a Detalles de la financiación: National Science and Technology Development Agency | ||
| 536 | |a Detalles de la financiación: Acknowledgements We gratefully thank Marcela F. Bolontrade PhD (Laboratory of Molecular and Cellular Therapy, Fundación In-stituto Leloir, Buenos Aires, Argentina) for providing HMEC-1 cells. This work was supported by the Grant PIP2011 from the National Council of Scientific and Technical Research (CONICET), Argentina; Grant PICT2006 from the National Agency for Science and Technology, Argentina; Grant 2006–2008, 2009–2011 and 2011–2013 from the Roemmers Foundation, Argentina; and the Institute for Regenerative Medicine, Texas A&M Health Science Center, Temple, Texas, USA. | ||
| 593 | |a Immunohematology Laboratory, Experimental Biology and Medicine Institute (IBYME), National Council of Scientific and Technical Research (CONICET), 2490 Vuelta de Obligado, 1428 Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina | ||
| 593 | |a Texas AandM Health Science Center, College of Medicine, Institute for Regenerative Medicine at Scott and White, 5701 Airport Road, Temple, TX 76502, United States | ||
| 593 | |a Department of Bone Marrow Transplantation, Favaloro Fundation, 443 Solis, 1428 Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina | ||
| 593 | |a Department of Oncology, Iriarte Hospital, 770 Alison Bell, 1878 Quilmes Buenos Aires, Argentina | ||
| 593 | |a Department of Oncology, Central Militar Hospital, 726 Luis María Campos, 1426 Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina | ||
| 593 | |a Department of Hemotherapy, Central Militar Hospital, 726 Luis María Campos, 1426 Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina | ||
| 593 | |a Department of Diagnosis and Treatment, Central Militar Hospital, 726 Luis María Campos, 1426 Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a BONE MARROW |
| 690 | 1 | 0 | |a BONE METASTASIS |
| 690 | 1 | 0 | |a BREAST CANCER |
| 690 | 1 | 0 | |a MESENCHYMAL STEM CELLS |
| 690 | 1 | 0 | |a PRE-METASTATIC NICHE |
| 690 | 1 | 0 | |a APOPTOSIS |
| 690 | 1 | 0 | |a BONE MARROW |
| 690 | 1 | 0 | |a BONE NEOPLASMS |
| 690 | 1 | 0 | |a BREAST NEOPLASMS |
| 690 | 1 | 0 | |a CELL LINE, TUMOR |
| 690 | 1 | 0 | |a CELL PROLIFERATION |
| 690 | 1 | 0 | |a ENZYME-LINKED IMMUNOSORBENT ASSAY |
| 690 | 1 | 0 | |a FEMALE |
| 690 | 1 | 0 | |a HUMANS |
| 690 | 1 | 0 | |a IMMUNOHISTOCHEMISTRY |
| 690 | 1 | 0 | |a NEOPLASM METASTASIS |
| 700 | 1 | |a Vallone, V.B.F. | |
| 700 | 1 | |a Labovsky, V. | |
| 700 | 1 | |a Choi, H. | |
| 700 | 1 | |a Hofer, E.L. | |
| 700 | 1 | |a Feldman, L. | |
| 700 | 1 | |a Bordenave, R.H. | |
| 700 | 1 | |a Batagelj, E. | |
| 700 | 1 | |a Dimase, F. | |
| 700 | 1 | |a Villafañe, A.R. | |
| 700 | 1 | |a Chasseing, N.A. | |
| 773 | 0 | |d 2014 |g v. 31 |h pp. 213-232 |k n. 2 |p Clin. Exp. Metastasis |x 02620898 |t Clinical and Experimental Metastasis | |
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| 856 | 4 | 0 | |u https://doi.org/10.1007/s10585-013-9622-5 |y DOI |
| 856 | 4 | 0 | |u https://hdl.handle.net/20.500.12110/paper_02620898_v31_n2_p213_Martinez |y Handle |
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| 961 | |a paper_02620898_v31_n2_p213_Martinez |b paper |c PE | ||
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| 999 | |c 84841 | ||