LGR6 is a prognostic biomarker for less differentiated tumors in lymph nodes of colon cancer patients.

CEA CXCL16 LGR5 LGR6 cancer stem cells colon cancer qRT-PCR regional lymph nodes

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2024
Historique:
received: 28 02 2024
accepted: 04 04 2024
medline: 8 5 2024
pubmed: 8 5 2024
entrez: 8 5 2024
Statut: epublish

Résumé

The aim was to investigate whether the stem cell marker LGR6 has prognostic value in colon cancer, alone or in combination with the prognostic biomarkers CEA and CXCL16. LGR6 mRNA levels were determined in 370 half lymph nodes of 121 colon cancer patients. Ability to predict relapse after curative surgery was estimated by Kaplan-Meier survival model and Cox regression analyses. Patients with high LGR6 levels [LGR6(+)] had a decreased mean survival time of 11 months at 5-year follow-up and 47 months at 12-year follow-up, respectively, with hazard ratios of 3.2 and 2.8. LGR6 mRNA analysis added prognostic value to CEA and CXCL16 mRNA analysis. In the poor prognosis groups CEA(+) and CXCL16(+), further division was achieved by LGR6 analysis. LGR6(+) patients had a very poor prognosis. LGR6 also identified a small number of CEA(-), TNM stage I patients who relapsed suggesting stem cell origin of these tumors. LGR6 and LGR5 levels correlated strongly in lymph nodes of stage I and IV patients but not in stage II patients, suggesting that these stem cell markers are differentially regulated. This study highlights LGR6 as a useful prognostic biomarker independently and in combination with CEA, CXCL16 or LGR5 identifying different risk groups.

Identifiants

pubmed: 38715790
doi: 10.3389/fonc.2024.1393075
pmc: PMC11074358
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1393075

Informations de copyright

Copyright © 2024 Eltorky, AbdelMageed, Ismail, Zahran, Guirgis, Olsson, Lindmark, Hammarström, Hammarström and Sitohy.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Hagar Eltorky (H)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Department of Biochemistry, Faculty of Science, Zagazig University, Zagazig, Egypt.

Manar AbdelMageed (M)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Department of Pathology, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt.

Hager Ismail (H)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Department of Clinical Pathology, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt.

Faten Zahran (F)

Department of Biochemistry, Faculty of Science, Zagazig University, Zagazig, Egypt.

Adel Guirgis (A)

Department of Molecular Biology, Genetic Engineering, and Biotechnology Research Institute, University of Sadat City, Sadat, Menoufia, Egypt.

Lina Olsson (L)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Gudrun Lindmark (G)

Institution of Clinical Sciences, Lund University, Lund, Sweden.

Marie-Louise Hammarström (ML)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Sten Hammarström (S)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Basel Sitohy (B)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.

Classifications MeSH