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Correlation of clinicopathological features and LGR5 expression in colon adenocarcinoma.
Sato, Koichi; Uehara, Takeshi; Iwaya, Mai; Nakajima, Tomoyuki; Miyagawa, Yusuke; Ota, Hiroyoshi; Tanaka, Eiji.
Afiliação
  • Sato K; Department of Gastroenterology, National Hospital Organization, Shinshu Ueda Medical Center, Ueda, Japan.
  • Uehara T; Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan. Electronic address: tuehara@shinshu-u.ac.jp.
  • Iwaya M; Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Nakajima T; Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Miyagawa Y; First Department of Surgery, Shinshu University School of Medicine, Matsumoto, Japan.
  • Ota H; Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan; Department of Biomedical Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Tanaka E; Department for the Promotion of Regional Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Ann Diagn Pathol ; 48: 151587, 2020 Oct.
Article em En | MEDLINE | ID: mdl-32829068
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Adenocarcinoma / Neoplasias do Colo / Receptores Acoplados a Proteínas G Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Adenocarcinoma / Neoplasias do Colo / Receptores Acoplados a Proteínas G Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article