RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma

Metastasis is a complex process by which cancer cells escape from the primary tumor to colonize distant organs. RAC1 is a member of the RHO family of small guanosine triphosphatases that plays an important role in cancer migration, invasion, angiogenesis and metastasis. RAC1 activation has been rela...

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Autores principales: Paula Colón-Bolea, Rocío García-Gómez, Berta Casar
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/51e13b68bf2940e4a3bc15a599bab654
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spelling oai:doaj.org-article:51e13b68bf2940e4a3bc15a599bab6542021-11-25T16:51:44ZRAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma10.3390/biom111115542218-273Xhttps://doaj.org/article/51e13b68bf2940e4a3bc15a599bab6542021-10-01T00:00:00Zhttps://www.mdpi.com/2218-273X/11/11/1554https://doaj.org/toc/2218-273XMetastasis is a complex process by which cancer cells escape from the primary tumor to colonize distant organs. RAC1 is a member of the RHO family of small guanosine triphosphatases that plays an important role in cancer migration, invasion, angiogenesis and metastasis. RAC1 activation has been related to most cancers, such as cutaneous melanoma, breast, lung, and pancreatic cancer. RAC1P29S driver mutation appears in a significant number of cutaneous melanoma cases. Likewise, RAC1 is overexpressed or hyperactivated via signaling through oncogenic cell surface receptors. Thus, targeting RAC1 represents a promising strategy for cutaneous melanoma therapy, as well as for inhibition of other signaling activation that promotes resistance to targeted therapies. In this review, we focus on the role of RAC1 in metastatic cutaneous melanoma emphasizing the anti-metastatic potential of RAC1- targeting drugs.Paula Colón-BoleaRocío García-GómezBerta CasarMDPI AGarticleRAC1cutaneous melanomainvasionmetastasistherapy resistanceMicrobiologyQR1-502ENBiomolecules, Vol 11, Iss 1554, p 1554 (2021)
institution DOAJ
collection DOAJ
language EN
topic RAC1
cutaneous melanoma
invasion
metastasis
therapy resistance
Microbiology
QR1-502
spellingShingle RAC1
cutaneous melanoma
invasion
metastasis
therapy resistance
Microbiology
QR1-502
Paula Colón-Bolea
Rocío García-Gómez
Berta Casar
RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma
description Metastasis is a complex process by which cancer cells escape from the primary tumor to colonize distant organs. RAC1 is a member of the RHO family of small guanosine triphosphatases that plays an important role in cancer migration, invasion, angiogenesis and metastasis. RAC1 activation has been related to most cancers, such as cutaneous melanoma, breast, lung, and pancreatic cancer. RAC1P29S driver mutation appears in a significant number of cutaneous melanoma cases. Likewise, RAC1 is overexpressed or hyperactivated via signaling through oncogenic cell surface receptors. Thus, targeting RAC1 represents a promising strategy for cutaneous melanoma therapy, as well as for inhibition of other signaling activation that promotes resistance to targeted therapies. In this review, we focus on the role of RAC1 in metastatic cutaneous melanoma emphasizing the anti-metastatic potential of RAC1- targeting drugs.
format article
author Paula Colón-Bolea
Rocío García-Gómez
Berta Casar
author_facet Paula Colón-Bolea
Rocío García-Gómez
Berta Casar
author_sort Paula Colón-Bolea
title RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma
title_short RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma
title_full RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma
title_fullStr RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma
title_full_unstemmed RAC1 Activation as a Potential Therapeutic Option in Metastatic Cutaneous Melanoma
title_sort rac1 activation as a potential therapeutic option in metastatic cutaneous melanoma
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/51e13b68bf2940e4a3bc15a599bab654
work_keys_str_mv AT paulacolonbolea rac1activationasapotentialtherapeuticoptioninmetastaticcutaneousmelanoma
AT rociogarciagomez rac1activationasapotentialtherapeuticoptioninmetastaticcutaneousmelanoma
AT bertacasar rac1activationasapotentialtherapeuticoptioninmetastaticcutaneousmelanoma
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