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Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments

The neurofibromatosis syndromes, including NF1, NF2, and schwannomatosis, are tumor suppressor syndromes characterized by multiple nervous system tumors, particularly Schwann cell neoplasms. NF-related tumors are mainly treated by surgery, and some of them have been treated by but are refractory to...

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Autores principales: Amaravathi, Anusha, Oblinger, Janet L., Welling, D. Bradley, Kinghorn, A. Douglas, Chang, Long-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485038/
https://www.ncbi.nlm.nih.gov/pubmed/34604034
http://dx.doi.org/10.3389/fonc.2021.698192
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author Amaravathi, Anusha
Oblinger, Janet L.
Welling, D. Bradley
Kinghorn, A. Douglas
Chang, Long-Sheng
author_facet Amaravathi, Anusha
Oblinger, Janet L.
Welling, D. Bradley
Kinghorn, A. Douglas
Chang, Long-Sheng
author_sort Amaravathi, Anusha
collection PubMed
description The neurofibromatosis syndromes, including NF1, NF2, and schwannomatosis, are tumor suppressor syndromes characterized by multiple nervous system tumors, particularly Schwann cell neoplasms. NF-related tumors are mainly treated by surgery, and some of them have been treated by but are refractory to conventional chemotherapy. Recent advances in molecular genetics and genomics alongside the development of multiple animal models have provided a better understanding of NF tumor biology and facilitated target identification and therapeutic evaluation. Many targeted therapies have been evaluated in preclinical models and patients with limited success. One major advance is the FDA approval of the MEK inhibitor selumetinib for the treatment of NF1-associated plexiform neurofibroma. Due to their anti-neoplastic, antioxidant, and anti-inflammatory properties, selected natural compounds could be useful as a primary therapy or as an adjuvant therapy prior to or following surgery and/or radiation for patients with tumor predisposition syndromes, as patients often take them as dietary supplements and for health enhancement purposes. Here we review the natural compounds that have been evaluated in NF models. Some have demonstrated potent anti-tumor effects and may become viable treatments in the future.
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spelling pubmed-84850382021-10-02 Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments Amaravathi, Anusha Oblinger, Janet L. Welling, D. Bradley Kinghorn, A. Douglas Chang, Long-Sheng Front Oncol Oncology The neurofibromatosis syndromes, including NF1, NF2, and schwannomatosis, are tumor suppressor syndromes characterized by multiple nervous system tumors, particularly Schwann cell neoplasms. NF-related tumors are mainly treated by surgery, and some of them have been treated by but are refractory to conventional chemotherapy. Recent advances in molecular genetics and genomics alongside the development of multiple animal models have provided a better understanding of NF tumor biology and facilitated target identification and therapeutic evaluation. Many targeted therapies have been evaluated in preclinical models and patients with limited success. One major advance is the FDA approval of the MEK inhibitor selumetinib for the treatment of NF1-associated plexiform neurofibroma. Due to their anti-neoplastic, antioxidant, and anti-inflammatory properties, selected natural compounds could be useful as a primary therapy or as an adjuvant therapy prior to or following surgery and/or radiation for patients with tumor predisposition syndromes, as patients often take them as dietary supplements and for health enhancement purposes. Here we review the natural compounds that have been evaluated in NF models. Some have demonstrated potent anti-tumor effects and may become viable treatments in the future. Frontiers Media S.A. 2021-09-17 /pmc/articles/PMC8485038/ /pubmed/34604034 http://dx.doi.org/10.3389/fonc.2021.698192 Text en Copyright © 2021 Amaravathi, Oblinger, Welling, Kinghorn and Chang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Amaravathi, Anusha
Oblinger, Janet L.
Welling, D. Bradley
Kinghorn, A. Douglas
Chang, Long-Sheng
Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments
title Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments
title_full Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments
title_fullStr Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments
title_full_unstemmed Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments
title_short Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments
title_sort neurofibromatosis: molecular pathogenesis and natural compounds as potential treatments
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485038/
https://www.ncbi.nlm.nih.gov/pubmed/34604034
http://dx.doi.org/10.3389/fonc.2021.698192
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