Your browser doesn't support javascript.
loading
Genomic and Pathologic Profiling of Very Well-Differentiated Gastric Adenocarcinoma of Intestinal Type: A Study With Emphasis on Diffuse-Type Transformation.
Rokutan, Hirofumi; Arai, Yasuhito; Kunita, Akiko; Yamasaki, Satoshi; Nakamura, Hiromi; Hama, Natsuko; Nakayama, Atsuhito; Hosoda, Fumie; Totoki, Yasushi; Fujishiro, Mitsuhiro; Seto, Yasuyuki; Shibata, Tatsuhiro; Ushiku, Tetsuo.
Afiliación
  • Rokutan H; Departments of Pathology.
  • Arai Y; Division of Cancer Genomics, National Cancer Center Research Institute, Tokyo.
  • Kunita A; Departments of Pathology.
  • Yamasaki S; Laboratory of Molecular Medicine, The Institute of Medical Science, The University of Tokyo.
  • Nakamura H; Division of Cancer Genomics, National Cancer Center Research Institute, Tokyo.
  • Hama N; Division of Cancer Genomics, National Cancer Center Research Institute, Tokyo.
  • Nakayama A; Departments of Pathology.
  • Hosoda F; Division of Cancer Genomics, National Cancer Center Research Institute, Tokyo.
  • Totoki Y; Division of Cancer Genomics, National Cancer Center Research Institute, Tokyo.
  • Fujishiro M; Department of Cancer Genome Informatics, Graduate School of Medicine, Osaka University, Osaka, Tokyo, Japan.
  • Seto Y; Gastroenterology.
  • Shibata T; Gastrointestinal Surgery.
  • Ushiku T; Laboratory of Molecular Medicine, The Institute of Medical Science, The University of Tokyo.
Am J Surg Pathol ; 48(6): 652-661, 2024 Jun 01.
Article en En | MEDLINE | ID: mdl-38584451
ABSTRACT
Very well-differentiated adenocarcinoma of intestinal type is a distinct subtype of gastric cancer characterized by anastomosing glands with a hand-in-hand pattern and low-grade cytologic atypia resembling intestinal metaplasia. This is a slow-growing neoplasm with an indolent clinical course; however, a subset demonstrates transformation into adenocarcinoma with higher-grade histology, typically diffuse-type carcinoma, and behaves aggressively. This study aimed to better characterize the genomic and pathologic features, with a focus on factors associated with diffuse-type transformation. A total of 58 cases with (n=31) and without (n=27) diffuse-type transformation were analyzed for molecular and pathologic features. First, comprehensive deep DNA sequencing was conducted in 18 cases (discovery cohort), followed by a digital droplet polymerase chain reaction of hot spot RHOA mutations in 40 cases (validation cohort). In total, RHOA mutations were the most common alteration (34%), followed by loss of ARID1A (12%), p53 alterations (10%), and CLDN18 ARHGAP26/6 fusions (3.4%). FGFR2 amplification was identified in an advanced case with a p53 alteration. Altered p53 expression was recognized only in higher-grade components and was significantly associated with advanced disease ( P =0.0015) and diffuse-type transformation ( P =0.026). A mixed mucin phenotype was also strongly correlated with advanced disease ( P <0.001) and diffuse-type transformation ( P <0.001). Decreased E-cadherin expression was frequently observed (74%) in poorly cohesive components. This study demonstrated that a subset of RHOA -mutant diffuse-type gastric cancers develops through the transformation of very well-differentiated adenocarcinoma of intestinal type. Our observations suggest a mixed mucin phenotype as a risk factor and alterations in p53 and E-cadherin as drivers of diffuse-type transformation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Gástricas / Adenocarcinoma / Biomarcadores de Tumor / Transformación Celular Neoplásica / Mutación Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Surg Pathol Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Gástricas / Adenocarcinoma / Biomarcadores de Tumor / Transformación Celular Neoplásica / Mutación Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Surg Pathol Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos