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      The Neurokinin-1 Receptor Antagonist Aprepitant: An Intelligent Bullet against Cancer?

      review-article
      1 , 2 , *
      Cancers
      MDPI
      apoptosis, antitumor, antimetastasis, anti-angiogenesis, NK-1 receptor, substance P, drug repositioning, Emend

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          Abstract

          Simple Summary

          Due to the lack of selectivity and the severe side-effects, cytostatics are the drugs of the present but not of the future and consequently new anticancer strategies must be developed. After binding to the neurokinin-1 receptor (NK-1R), NK-1R antagonists exert antitumor actions (antiproliferative, antimetastasis), are safe and do not cause serious side-effects. Aprepitant, a non-peptide NK-1R antagonist, is currently used in clinical practice as antiemetic but this compound also shows antitumor effects against a broad-spectrum of cancers. Our aim is to review the multiple antitumor actions exerted by aprepitant and to show the potential use of this drug as an antitumor agent. Aprepitant could be considered as an intelligent bullet against cancer. The data support the reprofiling of aprepitant for a new therapeutic use as an antitumor agent. The administration of aprepitant in cancer patients to prevent recurrence/metastasis after surgical procedures, thrombosis and thromboembolism is also suggested.

          Abstract

          Neurokinin-1 receptor (NK-1R) antagonists exert antitumor action, are safe and do not cause serious side-effects. These antagonists (via the NK-1R) exert multiple actions against cancer: antiproliferative and anti-Warburg effects and apoptotic, anti-angiogenic and antimetastatic effects. These multiple effects have been shown for a broad spectrum of cancers. The drug aprepitant (an NK-1R antagonist) is currently used in clinical practice as an antiemetic. In in vivo and in vitro studies, aprepitant also showed the aforementioned multiple antitumor actions against many types of cancer. A successful combination therapy (aprepitant and radiotherapy) has recently been reported in a patient suffering from lung carcinoma: the tumor mass disappeared and side-effects were not observed. Aprepitant could be considered as an intelligent bullet against cancer. The administration of aprepitant in cancer patients to prevent recurrence and metastasis after surgical procedures, thrombosis and thromboembolism is discussed, as is the possible link, through the substance P (SP)/NK-1R system, between cancer and depression. Our main aim is to review the multiple antitumor actions exerted by aprepitant, and the use of this drug is suggested in cancer patients. Altogether, the data support the reprofiling of aprepitant for a new therapeutic use as an antitumor agent.

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          Metastasis: a question of life or death.

          The metastatic process is highly inefficient--very few of the many cells that migrate from the primary tumour successfully colonize distant sites. One proposed mechanism to explain this inefficiency is provided by the cancer stem cell model, which hypothesizes that micrometastases can only be established by tumour stem cells, which are few in number. However, recent in vitro and in vivo observations indicate that apoptosis is an important process regulating metastasis. Here we stress that the inhibition of cell death, apart from its extensively described function in primary tumour development, is a crucial characteristic of metastatic cancer cells.
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            FoxM1 promotes β-catenin nuclear localization and controls Wnt target-gene expression and glioma tumorigenesis.

            Wnt/β-catenin signaling is essential for stem cell regulation and tumorigenesis, but its molecular mechanisms are not fully understood. Here, we report that FoxM1 is a downstream component of Wnt signaling and is critical for β-catenin transcriptional function in tumor cells. Wnt3a increases the level and nuclear translocation of FoxM1, which binds directly to β-catenin and enhances β-catenin nuclear localization and transcriptional activity. Genetic deletion of FoxM1 in immortalized neural stem cells abolishes β-catenin nuclear localization. FoxM1 mutations that disrupt the FoxM1-β-catenin interaction or FoxM1 nuclear import prevent β-catenin nuclear accumulation in tumor cells. FoxM1-β-catenin interaction controls Wnt target gene expression, is required for glioma formation, and represents a mechanism for canonical Wnt signaling during tumorigenesis. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Thromboembolism is a leading cause of death in cancer patients receiving outpatient chemotherapy.

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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                20 September 2020
                September 2020
                : 12
                : 9
                : 2682
                Affiliations
                [1 ]Research Laboratory on Neuropeptides (IBIS), Virgen del Rocío University Hospital, 41013 Sevilla, Spain; mmunoz@ 123456cica.es
                [2 ]Institute of Neurosciences of Castilla y León (INCYL), Laboratory of Neuroanatomy of the Peptidergic Systems, University of Salamanca, c/ Pintor Fernando Gallego, 1, 37007 Salamanca, Spain
                Author notes
                [* ]Correspondence: covenas@ 123456usal.es ; Tel.: +34-923-294-400
                Author information
                https://orcid.org/0000-0002-2853-8481
                https://orcid.org/0000-0001-5677-8266
                Article
                cancers-12-02682
                10.3390/cancers12092682
                7564414
                32962202
                5b88d937-c586-44a7-8660-0ec6582abb30
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 August 2020
                : 17 September 2020
                Categories
                Review

                apoptosis,antitumor,antimetastasis,anti-angiogenesis,nk-1 receptor,substance p,drug repositioning,emend

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