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Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies

Acute myeloid leukemia (AML) arises from neoplastic transformation of hematopoietic stem and progenitor cells, and relapsed disease remains one of the greater challenges in treating this hematologic malignancy. This paper focuses on angiogenic aspects of AML including the significance and prognostic...

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Detalles Bibliográficos
Autores principales: Trujillo, Angelica, McGee, Christie, Cogle, Christopher R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167188/
https://www.ncbi.nlm.nih.gov/pubmed/21904549
http://dx.doi.org/10.1155/2012/128608
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author Trujillo, Angelica
McGee, Christie
Cogle, Christopher R.
author_facet Trujillo, Angelica
McGee, Christie
Cogle, Christopher R.
author_sort Trujillo, Angelica
collection PubMed
description Acute myeloid leukemia (AML) arises from neoplastic transformation of hematopoietic stem and progenitor cells, and relapsed disease remains one of the greater challenges in treating this hematologic malignancy. This paper focuses on angiogenic aspects of AML including the significance and prognostic value of bone marrow microvessel density and circulating cytokine levels. We show three general mechanisms whereby AML exploits angiogenic pathways, including direct induction of angiogenesis, paracrine regulation, and autocrine stimulation. We also present early evidence that leukemia cells contribute directly to vascular endothelia. Novel treatment strategies are proposed, and a review of relevant antiangiogenic clinical trials is presented. By understanding how blood vessels can serve as a reservoir for refractory and relapsed AML, new diagnostics and promising treatment strategies can be developed.
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spelling pubmed-31671882011-09-08 Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies Trujillo, Angelica McGee, Christie Cogle, Christopher R. J Oncol Review Article Acute myeloid leukemia (AML) arises from neoplastic transformation of hematopoietic stem and progenitor cells, and relapsed disease remains one of the greater challenges in treating this hematologic malignancy. This paper focuses on angiogenic aspects of AML including the significance and prognostic value of bone marrow microvessel density and circulating cytokine levels. We show three general mechanisms whereby AML exploits angiogenic pathways, including direct induction of angiogenesis, paracrine regulation, and autocrine stimulation. We also present early evidence that leukemia cells contribute directly to vascular endothelia. Novel treatment strategies are proposed, and a review of relevant antiangiogenic clinical trials is presented. By understanding how blood vessels can serve as a reservoir for refractory and relapsed AML, new diagnostics and promising treatment strategies can be developed. Hindawi Publishing Corporation 2012 2011-09-05 /pmc/articles/PMC3167188/ /pubmed/21904549 http://dx.doi.org/10.1155/2012/128608 Text en Copyright © 2012 Angelica Trujillo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Trujillo, Angelica
McGee, Christie
Cogle, Christopher R.
Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies
title Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies
title_full Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies
title_fullStr Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies
title_full_unstemmed Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies
title_short Angiogenesis in Acute Myeloid Leukemia and Opportunities for Novel Therapies
title_sort angiogenesis in acute myeloid leukemia and opportunities for novel therapies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167188/
https://www.ncbi.nlm.nih.gov/pubmed/21904549
http://dx.doi.org/10.1155/2012/128608
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