Emerging targets in human lymphoma: targeting the MYD88 mutation

James Q Wang,* Yogesh S Jeelall,* Keisuke Horikawa* Department of Immunology, The John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia *All authors contributed equally to this manuscript Abstract: B cell neoplasms co-opt the molecular machinery of normal B...

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Autores principales: Wang JQ, Jeelall YS, Horikawa K
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Publicado: Dove Medical Press 2013
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spelling oai:doaj.org-article:ff4e0887c6a4423ab1ae6b7efdc73c1c2021-12-02T00:33:22ZEmerging targets in human lymphoma: targeting the MYD88 mutation1179-9889https://doaj.org/article/ff4e0887c6a4423ab1ae6b7efdc73c1c2013-08-01T00:00:00Zhttp://www.dovepress.com/emerging-targets-in-human-lymphoma-targeting-the-myd88-mutation-a14017https://doaj.org/toc/1179-9889James Q Wang,* Yogesh S Jeelall,* Keisuke Horikawa* Department of Immunology, The John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia *All authors contributed equally to this manuscript Abstract: B cell neoplasms co-opt the molecular machinery of normal B cells for their survival. Technological advances in cancer genomics has significantly contributed to uncovering the root cause of aggressive lymphomas, revealing a previously unknown link between TLR signaling and B cell neoplasm. Recurrent oncogenic mutations in MYD88 have been found in 39% of the activated B cell-like subtype of diffuse large B cell lymphoma (ABC DLBCL). Interestingly, 29% of ABC DLBCL have a single amino acid substitution of proline for the leucine at position 265 (L265P), and the exact same variant has also been identified in a number of lymphoid malignancies. The MYD88 L265P variant was recently identified in 90% of Wadenstrom's macroglobulinemia patients. These recent developments warrant the need for novel diagnostic tools as well as targeted therapeutics. In this review, we discuss the physiological functions of MYD88 and focus on its role in B cell lymphomas, evaluating the potential for targeting oncogenic MYD88 in lymphoma. Keywords: MYD88, L265P mutation, lymphoma, targeted therapyWang JQJeelall YSHorikawa KDove Medical PressarticleDiseases of the blood and blood-forming organsRC633-647.5ENBlood and Lymphatic Cancer: Targets and Therapy, Vol 2013, Iss default, Pp 53-61 (2013)
institution DOAJ
collection DOAJ
language EN
topic Diseases of the blood and blood-forming organs
RC633-647.5
spellingShingle Diseases of the blood and blood-forming organs
RC633-647.5
Wang JQ
Jeelall YS
Horikawa K
Emerging targets in human lymphoma: targeting the MYD88 mutation
description James Q Wang,* Yogesh S Jeelall,* Keisuke Horikawa* Department of Immunology, The John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia *All authors contributed equally to this manuscript Abstract: B cell neoplasms co-opt the molecular machinery of normal B cells for their survival. Technological advances in cancer genomics has significantly contributed to uncovering the root cause of aggressive lymphomas, revealing a previously unknown link between TLR signaling and B cell neoplasm. Recurrent oncogenic mutations in MYD88 have been found in 39% of the activated B cell-like subtype of diffuse large B cell lymphoma (ABC DLBCL). Interestingly, 29% of ABC DLBCL have a single amino acid substitution of proline for the leucine at position 265 (L265P), and the exact same variant has also been identified in a number of lymphoid malignancies. The MYD88 L265P variant was recently identified in 90% of Wadenstrom's macroglobulinemia patients. These recent developments warrant the need for novel diagnostic tools as well as targeted therapeutics. In this review, we discuss the physiological functions of MYD88 and focus on its role in B cell lymphomas, evaluating the potential for targeting oncogenic MYD88 in lymphoma. Keywords: MYD88, L265P mutation, lymphoma, targeted therapy
format article
author Wang JQ
Jeelall YS
Horikawa K
author_facet Wang JQ
Jeelall YS
Horikawa K
author_sort Wang JQ
title Emerging targets in human lymphoma: targeting the MYD88 mutation
title_short Emerging targets in human lymphoma: targeting the MYD88 mutation
title_full Emerging targets in human lymphoma: targeting the MYD88 mutation
title_fullStr Emerging targets in human lymphoma: targeting the MYD88 mutation
title_full_unstemmed Emerging targets in human lymphoma: targeting the MYD88 mutation
title_sort emerging targets in human lymphoma: targeting the myd88 mutation
publisher Dove Medical Press
publishDate 2013
url https://doaj.org/article/ff4e0887c6a4423ab1ae6b7efdc73c1c
work_keys_str_mv AT wangjq emergingtargetsinhumanlymphomatargetingthemyd88mutation
AT jeelallys emergingtargetsinhumanlymphomatargetingthemyd88mutation
AT horikawak emergingtargetsinhumanlymphomatargetingthemyd88mutation
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