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L-amino acid transporter 1 may be a prognostic marker for local progression of prostatic cancer under expectant management.
Yanagisawa, Nobuyuki; Satoh, Takefumi; Hana, Kiyomi; Ichinoe, Masaaki; Nakada, Norihiro; Endou, Hitoshi; Okayasu, Isao; Murakumo, Yoshiki.
Afiliación
  • Yanagisawa N; Department of Pathology, Kitasato University School of Medicine, Kanagawa, Japan.
  • Satoh T; Department of Pathology of Biological Responses, Kitasato University Graduate School of Medical Science, Kanagawa, Japan.
  • Hana K; Department of Urology, Kitasato University School of Medicine, Kanagawa, Japan.
  • Ichinoe M; J-Pharma Co., Ltd., Kanagawa, Japan.
  • Nakada N; Department of Pathology, Kitasato University School of Medicine, Kanagawa, Japan.
  • Endou H; Department of Pathology of Biological Responses, Kitasato University Graduate School of Medical Science, Kanagawa, Japan.
  • Okayasu I; Department of Pathology, Kitasato University School of Medicine, Kanagawa, Japan.
  • Murakumo Y; Department of Pathology of Biological Responses, Kitasato University Graduate School of Medical Science, Kanagawa, Japan.
Cancer Biomark ; 15(4): 365-74, 2015.
Article en En | MEDLINE | ID: mdl-25835180
ABSTRACT

BACKGROUND:

Oncocytic L-amino acid transporter (LAT) 1 could be a target of new molecular therapy against malignancies.

OBJECTIVE:

To assess the correlation between overexpression of LAT1 and local progression (LP) in prostatic carcinoma (PC) patients under expectant management (EM).

METHODS:

This retrospective study analyzed 109 patients with PC who received EM from 1991 to 2006. The expression of LAT1, LAT2, and CD98, as well as Ki-67 labeling indices (LI), was analyzed immunohistochemically in first biopsy or TUR samples diagnosed as adenocarcinomas.

RESULTS:

Of the 109 patients, 44 (40%) showed LP on clinical examinations, whereas 65 showed stable disease (SD). LAT1 score and intensity were significantly higher in the LP than in the SD group, as well as among Gleason score (GS)-low (GS < 7) patients who were associated with low-risk. When the LP group was subdivided by D'Amico risk category (low-, intermediate- and high-risk groups), each showed higher LAT1 expression than the SD group. LAT1 expression did not correlate with GS or Ki-67 LI.

CONCLUSIONS:

Independently of GS, aberrant overexpression of LAT1 in prostatic adenocarcinoma could predict LP under EM. Although prostate biopsy samples are small, LAT1 may be a novel prognostic biomarker of LP.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Adenocarcinoma / Biomarcadores de Tumor / Transportador de Aminoácidos Neutros Grandes 1 Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Cancer Biomark Asunto de la revista: BIOQUIMICA / NEOPLASIAS Año: 2015 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Adenocarcinoma / Biomarcadores de Tumor / Transportador de Aminoácidos Neutros Grandes 1 Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Cancer Biomark Asunto de la revista: BIOQUIMICA / NEOPLASIAS Año: 2015 Tipo del documento: Article País de afiliación: Japón