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LGR6 is a prognostic biomarker for less differentiated tumors in lymph nodes of colon cancer patients.
Eltorky, Hagar; AbdelMageed, Manar; Ismail, Hager; Zahran, Faten; Guirgis, Adel; Olsson, Lina; Lindmark, Gudrun; Hammarström, Marie-Louise; Hammarström, Sten; Sitohy, Basel.
Afiliação
  • Eltorky H; Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
  • AbdelMageed M; Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
  • Ismail H; Department of Biochemistry, Faculty of Science, Zagazig University, Zagazig, Egypt.
  • Zahran F; Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
  • Guirgis A; Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
  • Olsson L; Department of Pathology, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt.
  • Lindmark G; Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
  • Hammarström ML; Department of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
  • Hammarström S; Department of Clinical Pathology, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt.
  • Sitohy B; Department of Biochemistry, Faculty of Science, Zagazig University, Zagazig, Egypt.
Front Oncol ; 14: 1393075, 2024.
Article em En | MEDLINE | ID: mdl-38715790
ABSTRACT

Introduction:

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.

Methods:

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.

Results:

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.

Conclusion:

This study highlights LGR6 as a useful prognostic biomarker independently and in combination with CEA, CXCL16 or LGR5 identifying different risk groups.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article