Neurotensin Receptor-1 Expression in Human Prostate Cancer: A Pilot Study on Primary Tumors and Lymph Node Metastases.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
07 Apr 2019
Historique:
received: 01 03 2019
revised: 27 03 2019
accepted: 01 04 2019
entrez: 10 4 2019
pubmed: 10 4 2019
medline: 28 7 2019
Statut: epublish

Résumé

Neurotensin and its high-affinity receptor, NTR₁, are involved in the growth of various tumors. Few data are available regarding NTR₁ expression in normal and tumoral human prostate tissue samples. NTR₁ expression was assessed using immunohistochemistry in 12 normal prostate tissues, 11 benign prostatic hyperplasia (BPH), 44 prostate cancers, and 15 related metastatic lymph nodes (one per patient, when available). NTR₁-staining was negative in normal prostate and BPH samples. NTR₁ was overexpressed in four out of 44 (9.1%) primary tumors. There was no clear association between NTR₁ overexpression and age, PSA-values, Gleason score, pT-status, nodal-status, or margin. NTR₁ was expressed at a high level of five out of 15 (33.3%) metastatic lymph nodes. NTR₁ overexpression was thus more frequent in metastatic lymph nodes than in primary tumors (

Identifiants

pubmed: 30959962
pii: ijms20071721
doi: 10.3390/ijms20071721
pmc: PMC6479796
pii:
doi:

Substances chimiques

Neuropeptides 0
Receptors, Neurotensin 0
neurotensin type 1 receptor 0

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : TRAIL
ID : ANR-10-LABX-57

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Auteurs

Clément Morgat (C)

CNRS, INCIA, UMR 5287, F-33000 Bordeaux, France. clement.morgat@u-bordeaux.fr.
University of Bordeaux, INCIA, UMR 5287, F-33000 Bordeaux, France. clement.morgat@u-bordeaux.fr.
Department of Nuclear Medicine, University Hospital of Bordeaux, F-33000 Bordeaux, France. clement.morgat@u-bordeaux.fr.

Adrien Chastel (A)

CNRS, INCIA, UMR 5287, F-33000 Bordeaux, France. adrien.chastel@chu-bordeaux.fr.
University of Bordeaux, INCIA, UMR 5287, F-33000 Bordeaux, France. adrien.chastel@chu-bordeaux.fr.
Department of Nuclear Medicine, University Hospital of Bordeaux, F-33000 Bordeaux, France. adrien.chastel@chu-bordeaux.fr.

Vincent Molinie (V)

Department of Pathology, University Hospital of Martinique, 97261 Fort de France, France. Vincent.MOLINIE@chu-martinique.fr.

Romain Schollhammer (R)

CNRS, INCIA, UMR 5287, F-33000 Bordeaux, France. romain.scho@gmail.com.
University of Bordeaux, INCIA, UMR 5287, F-33000 Bordeaux, France. romain.scho@gmail.com.
Department of Nuclear Medicine, University Hospital of Bordeaux, F-33000 Bordeaux, France. romain.scho@gmail.com.

Gaétan Macgrogan (G)

Surgical Pathology unit, Department of BioPathology, Institut Bergonié, F-33076 Bordeaux, France. G.MacGrogan@bordeaux.unicancer.fr.
INSERM, ACTION U1218, F-33076 Bordeaux, France. G.MacGrogan@bordeaux.unicancer.fr.

Valérie Vélasco (V)

Surgical Pathology unit, Department of BioPathology, Institut Bergonié, F-33076 Bordeaux, France. V.Velasco@bordeaux.unicancer.fr.
INSERM, ACTION U1218, F-33076 Bordeaux, France. V.Velasco@bordeaux.unicancer.fr.

Bernard Malavaud (B)

Department of Urology, University Hospital of Toulouse, F-31000 Toulouse, France. bernard.malavaud@me.com.

Philippe Fernandez (P)

CNRS, INCIA, UMR 5287, F-33000 Bordeaux, France. philippe.fernandez@chu-bordeaux.fr.
University of Bordeaux, INCIA, UMR 5287, F-33000 Bordeaux, France. philippe.fernandez@chu-bordeaux.fr.
Department of Nuclear Medicine, University Hospital of Bordeaux, F-33000 Bordeaux, France. philippe.fernandez@chu-bordeaux.fr.

Elif Hindié (E)

CNRS, INCIA, UMR 5287, F-33000 Bordeaux, France. elif.hindie@chu-bordeaux.fr.
University of Bordeaux, INCIA, UMR 5287, F-33000 Bordeaux, France. elif.hindie@chu-bordeaux.fr.
Department of Nuclear Medicine, University Hospital of Bordeaux, F-33000 Bordeaux, France. elif.hindie@chu-bordeaux.fr.

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