Neurotensin and its high affinity receptor 1 as a potential pharmacological target in cancer therapy
Identifieur interne : 000C78 ( Main/Exploration ); précédent : 000C77; suivant : 000C79Neurotensin and its high affinity receptor 1 as a potential pharmacological target in cancer therapy
Auteurs : Zherui Wu [France] ; Daniel Martinez-Fong [Mexique] ; Jean Trédaniel [France] ; Patricia Forgez [France]Source :
- Frontiers in Endocrinology [ 1664-2392 ] ; 2013.
Abstract
Cancer is a worldwide health problem. Personalized treatment represents a future advancement for cancer treatment, in part due to the development of targeted therapeutic drugs. These molecules are expected to be more effective than current treatments and less harmful to normal cells. The discovery and validation of new targets are the foundation and the source of these new therapies. The neurotensinergic system has been shown to enhance cancer progression in various cancers such as pancreatic, prostate, lung, breast, and colon cancer. It also triggers multiple oncogenic signaling pathways, such as the PKC/ERK and AKT pathways. In this review, we discuss the contribution of the neurotensinergic system to cancer progression, as well as the regulation and mechanisms of the system in order to highlight its potential as a therapeutic target, and its prospect for its use as a treatment in certain cancers.
Url:
DOI: 10.3389/fendo.2012.00184
PubMed: 23335914
PubMed Central: 3547287
Affiliations:
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wicri:level="1"><nlm:aff id="aff2"><institution>Departamento de Fisiologïa, Biofïsica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional</institution><country>Mexico City, Mexico</country></nlm:aff><country xml:lang="fr">Mexique</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Tredaniel, Jean" sort="Tredaniel, Jean" uniqKey="Tredaniel J" first="Jean" last="Trédaniel">Jean Trédaniel</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>INSERM-UPMC UMR_S938, Hôpital Saint-Antoine</institution><country>Paris, France</country></nlm:aff><country xml:lang="fr">France</country><wicri:regionArea></wicri:regionArea></affiliation><affiliation wicri:level="1"><nlm:aff id="aff3"><institution>Unité de Cancérologie Thoracique, Groupe Hospitalier Paris Saint-Joseph/Université Paris Descartes</institution><country>Paris, France</country></nlm:aff><country xml:lang="fr">France</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Forgez, Patricia" sort="Forgez, Patricia" uniqKey="Forgez P" first="Patricia" last="Forgez">Patricia Forgez</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>INSERM-UPMC UMR_S938, Hôpital Saint-Antoine</institution><country>Paris, France</country></nlm:aff><country xml:lang="fr">France</country><wicri:regionArea></wicri:regionArea></affiliation></author></analytic><series><title level="j">Frontiers in Endocrinology</title><idno type="eISSN">1664-2392</idno><imprint><date when="2013">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Cancer is a worldwide health problem. Personalized treatment represents a future advancement for cancer treatment, in part due to the development of targeted therapeutic drugs. These molecules are expected to be more effective than current treatments and less harmful to normal cells. The discovery and validation of new targets are the foundation and the source of these new therapies. The neurotensinergic system has been shown to enhance cancer progression in various cancers such as pancreatic, prostate, lung, breast, and colon cancer. It also triggers multiple oncogenic signaling pathways, such as the PKC/ERK and AKT pathways. In this review, we discuss the contribution of the neurotensinergic system to cancer progression, as well as the regulation and mechanisms of the system in order to highlight its potential as a therapeutic target, and its prospect for its use as a treatment in certain cancers.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Alifano, M" uniqKey="Alifano M">M. Alifano</name></author><author><name sortKey="Loi, M" uniqKey="Loi M">M. Loi</name></author><author><name sortKey="Camilleri Broet, S" uniqKey="Camilleri Broet S">S. Camilleri-Broet</name></author><author><name sortKey="Dupouy, S" uniqKey="Dupouy S">S. Dupouy</name></author><author><name sortKey="Regnard, J F" uniqKey="Regnard J">J. F. Regnard</name></author><author><name sortKey="Forgez, P" uniqKey="Forgez P">P. Forgez</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Alifano, M" uniqKey="Alifano M">M. 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Zeng</name></author><author><name sortKey="Wu, J S" uniqKey="Wu J">J. S. Wu</name></author><author><name sortKey="Moyer, M P" uniqKey="Moyer M">M. P. Moyer</name></author><author><name sortKey="Pothoulakis, C" uniqKey="Pothoulakis C">C. Pothoulakis</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhao, D" uniqKey="Zhao D">D. Zhao</name></author><author><name sortKey="Zhan, Y" uniqKey="Zhan Y">Y. Zhan</name></author><author><name sortKey="Zeng, H" uniqKey="Zeng H">H. Zeng</name></author><author><name sortKey="Koon, H W" uniqKey="Koon H">H. W. Koon</name></author><author><name sortKey="Moyer, M P" uniqKey="Moyer M">M. P. Moyer</name></author><author><name sortKey="Pothoulakis, C" uniqKey="Pothoulakis C">C. Pothoulakis</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>France</li><li>Mexique</li></country></list><tree><country name="France"><noRegion><name sortKey="Wu, Zherui" sort="Wu, Zherui" uniqKey="Wu Z" first="Zherui" last="Wu">Zherui Wu</name></noRegion><name sortKey="Forgez, Patricia" sort="Forgez, Patricia" uniqKey="Forgez P" first="Patricia" last="Forgez">Patricia Forgez</name><name sortKey="Tredaniel, Jean" sort="Tredaniel, Jean" uniqKey="Tredaniel J" first="Jean" last="Trédaniel">Jean Trédaniel</name><name sortKey="Tredaniel, Jean" sort="Tredaniel, Jean" uniqKey="Tredaniel J" first="Jean" last="Trédaniel">Jean Trédaniel</name></country><country name="Mexique"><noRegion><name sortKey="Martinez Fong, Daniel" sort="Martinez Fong, Daniel" uniqKey="Martinez Fong D" first="Daniel" last="Martinez-Fong">Daniel Martinez-Fong</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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