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Correlation of clinicopathological features and LGR5 expression in colon adenocarcinoma
Affiliation:1. Division of Colorectal Surgery, Department of Surgery, Oregon Health and Science University, 3181 S.W. Sam Jackson Park Road, L223A, Portland, OR 97239, USA;2. Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA;3. Integrated Genomics Laboratory, Oregon Health and Science University, Portland, OR, USA;4. Arizona Cancer Center, Tucson, AZ, USA;5. Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA;1. Department of Dermatology, Complejo Asistencial Universitario de León, León, Spain;2. University of León, León, Spain;3. Department of Immunology, Complejo Asistencial Universitario de León, León, Spain;4. Department of Dermatology, Hospital del Río Hortega, Valladolid, Spain
Abstract:Colon cancer stem cells (CSCs) are closely related to tumorigenesis and treatment response, and LGR5 is currently the most robust and reliable CSC marker in colorectal cancer (CRC). However, LGR5 expression in CRC tumor budding (TB) is not well understood. We examined the clinicopathological and prognostic significance of LGR5 in CRC TB. LGR5 expression was evaluated by RNAscope, a newly developed RNA in situ hybridization technique, using a tissue microarray consisting of 55 patient samples of TB in colon adenocarcinoma (CA) selected from the medical archives at our hospital. Patients were stratified into negative and positive LGR5 expression groups. Tumor-infiltrating lymphocytes (TILs) and histological grade were lower in the LGR5-positive group compared with the LGR5-negative group (P = .0407 and P = .0436, respectively). There was no significant difference in overall survival between the LGR5-positive group and the LGR5-negative group (log-rank test, P = .6931). LGR5 expression did not remain a predictor of prognosis in univariate analysis (OR = 0.84, 95% CI: 0.33–2.02, P = .6928). LGR5 expression may be affected by TILs, which have been demonstrated to be associated with worse prognosis in the budding area of CA and is an important potential marker of prognosis.
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