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ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development
With the advent of new agents targeting CD20, Bruton’s tyrosine kinase, and phosphoinositol-3 kinase for chronic lymphoid leukemia (CLL), more treatment options exist than ever before. B-cell lymphoma-2 (BCL-2) plays a major role in cellular apoptosis and is a druggable target. Small molecule inhibi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654800/ https://www.ncbi.nlm.nih.gov/pubmed/26589495 http://dx.doi.org/10.1186/s13045-015-0224-3 |
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author | Cang, Shundong Iragavarapu, Chaitanya Savooji, John Song, Yongping Liu, Delong |
author_facet | Cang, Shundong Iragavarapu, Chaitanya Savooji, John Song, Yongping Liu, Delong |
author_sort | Cang, Shundong |
collection | PubMed |
description | With the advent of new agents targeting CD20, Bruton’s tyrosine kinase, and phosphoinositol-3 kinase for chronic lymphoid leukemia (CLL), more treatment options exist than ever before. B-cell lymphoma-2 (BCL-2) plays a major role in cellular apoptosis and is a druggable target. Small molecule inhibitors of BCL-2 are in active clinical studies. ABT-199 (venetoclax, RG7601, GDC-0199) has been granted breakthrough designation by FDA for relapsed or refractory CLL with 17p deletion. In this review, we summarized the latest clinical development of ABT-199/venetoclax and other novel agents targeting the BCL-2 proteins. |
format | Online Article Text |
id | pubmed-4654800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46548002015-11-22 ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development Cang, Shundong Iragavarapu, Chaitanya Savooji, John Song, Yongping Liu, Delong J Hematol Oncol Review With the advent of new agents targeting CD20, Bruton’s tyrosine kinase, and phosphoinositol-3 kinase for chronic lymphoid leukemia (CLL), more treatment options exist than ever before. B-cell lymphoma-2 (BCL-2) plays a major role in cellular apoptosis and is a druggable target. Small molecule inhibitors of BCL-2 are in active clinical studies. ABT-199 (venetoclax, RG7601, GDC-0199) has been granted breakthrough designation by FDA for relapsed or refractory CLL with 17p deletion. In this review, we summarized the latest clinical development of ABT-199/venetoclax and other novel agents targeting the BCL-2 proteins. BioMed Central 2015-11-20 /pmc/articles/PMC4654800/ /pubmed/26589495 http://dx.doi.org/10.1186/s13045-015-0224-3 Text en © Cang et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Cang, Shundong Iragavarapu, Chaitanya Savooji, John Song, Yongping Liu, Delong ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development |
title | ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development |
title_full | ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development |
title_fullStr | ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development |
title_full_unstemmed | ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development |
title_short | ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development |
title_sort | abt-199 (venetoclax) and bcl-2 inhibitors in clinical development |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654800/ https://www.ncbi.nlm.nih.gov/pubmed/26589495 http://dx.doi.org/10.1186/s13045-015-0224-3 |
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