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Emerging roles and mechanisms of semaphorins activity in cancer.
Bica, Cecilia; Tirpe, Alexandru; Nutu, Andreea; Ciocan, Cristina; Chira, Sergiu; Gurzau, Eugen S; Braicu, Cornelia; Berindan-Neagoe, Ioana.
Afiliación
  • Bica C; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania. Electronic address: cecilia.bica8@gmail.com.
  • Tirpe A; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania; Faculty of Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, 8 Victor Babes Street, 400012 Cluj-Napoca, Romania. Electronic
  • Nutu A; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania. Electronic address: nutu.andreea@umfcluj.ro.
  • Ciocan C; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania. Electronic address: cristina.ciocan@umfcluj.ro.
  • Chira S; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania. Electronic address: sergiu.chira@umfcluj.ro.
  • Gurzau ES; Cluj School of Public Health, College of Political, Administrative and Communication Sciences, Babes-Bolyai University, 7 Pandurilor Street, Cluj-Napoca, Romania; Environmental Health Center, 58 Busuiocului Street, 400240 Cluj-Napoca, Romania. Electronic address: egurzau@ehc.ro.
  • Braicu C; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania. Electronic address: cornelia.braicu@umfcluj.ro.
  • Berindan-Neagoe I; Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca 400337, Romania. Electronic address: ioana.neagoe@umfcluj.ro.
Life Sci ; 318: 121499, 2023 Apr 01.
Article en En | MEDLINE | ID: mdl-36775114
ABSTRACT
Semaphorins are regulatory molecules that are linked to the modulation of several cancer processes, such as angiogenesis, cancer cell invasiveness and metastasis, tumor growth, as well as cancer cell survival. Semaphorin (SEMA) activity depends on the cancer histotypes and their particularities. In broad terms, the effects of SEMAs result from their interaction with specific receptors/co-receptors - Plexins, Neuropilins and Integrins - and the subsequent effects upon the downstream effectors (e.g. PI3K/AKT, MAPK/ERK). The present article serves as an integrative review work, discussing the broad implications of semaphorins in cancer, focusing on cell proliferation/survival, angiogenesis, invasion, metastasis, stemness, and chemo-resistance/response whilst highlighting their heterogeneity as a family. Herein, we emphasized that semaphorins are largely implicated in cancer progression, interacting with the tumor microenvironment components. Whilst some SEMAs (e.g. SEMA3A, SEMA3B) function widely as tumor suppressors, others (e.g. SEMA3C) act as pro-tumor semaphorins. The differences observed in terms of the biological structure of SEMAs and the particularities of each cancer histotypes require that each semaphorin be viewed as a unique entity, and its roles must be researched accordingly. A more in-depth and comprehensive view of the molecular mechanisms that promote and sustain the malignant behavior of cancer cells is of utmost importance.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Semaforinas / Neoplasias Límite: Humans Idioma: En Revista: Life Sci Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Semaforinas / Neoplasias Límite: Humans Idioma: En Revista: Life Sci Año: 2023 Tipo del documento: Article
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