Expression of Glucose Metabolism-Related Proteins in Adrenal Neoplasms.

Adrenal cortical adenoma Adrenal cortical carcinoma Glucose metabolism Immunohistochemistry Pheochromocytoma

Journal

Pathobiology : journal of immunopathology, molecular and cellular biology
ISSN: 1423-0291
Titre abrégé: Pathobiology
Pays: Switzerland
ID NLM: 9007504

Informations de publication

Date de publication:
2021
Historique:
received: 08 04 2021
accepted: 01 07 2021
pubmed: 15 9 2021
medline: 14 1 2022
entrez: 14 9 2021
Statut: ppublish

Résumé

The aim of this study was to investigate the expression patterns of glucose metabolism-related proteins and their clinicopathologic implications in adrenal cortical neoplasms (ACN) and pheochromocytoma (PCC). Immunohistochemical staining was performed to evaluate glucose metabolism-related proteins (GLUT1, CAIX, hexokinase II, G6PDH, PHGDH, and SHMT1) in 132 ACN cases (115 adrenal cortical adenoma [ACA] and 17 adrenal cortical carcinoma [ACC]) and 189 PCC cases. Expression levels of GLUT1 in tumor cells ([T]; p < 0.001), GLUT1 in stromal cells ([S]; p < 0.001), G6PDH (p < 0.001), and SHMT1 (p = 0.002) were higher in ACN than in PCC. GLUT1 (T; p = 0.045) and PHGDH (p = 0.043) levels were higher in ACC than in ACA. In a univariate analysis of ACN, GLUT1 (T; p = 0.017), CAIX (S; p = 0.003), and PHGDH (p = 0.009) levels were correlated with a shorter overall survival (OS). GLUT1 (T; p = 0.001) and PHGDH (p < 0.001) were related to a shorter OS in PCC. GLUT1 (T) positivity (p = 0.043) in ACN predicted a poor OS in a multivariate Cox analysis. In PCC, high GAPP score (p = 0.026), GLUT1 (T; p = 0.002), and PHGDH (p < 0.001) were independent prognostic factors for poor OS. The adrenal gland tumors ACN and PCC had different expression patterns of glucose metabolism-related proteins (GLUT1, G6PDH, and SHMT1), with higher expression levels in ACN than in PCC. GLUT1 and PHGDH were significant prognostic factors in these adrenal neoplasms.

Identifiants

pubmed: 34518477
pii: 000518208
doi: 10.1159/000518208
doi:

Substances chimiques

Glucose Transporter Type 1 0
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

424-433

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Eun Kyung Kim (EK)

Department of Pathology, National Health Insurance Service Ilsan Hospital, Goyang, Republic of Korea.

Hye Min Kim (HM)

Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.

Ja Seung Koo (JS)

Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.

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Classifications MeSH