Microsatellite instability in solitary and sporadic gastric cancer

Authors

  • Rodrigo Oliva Perez University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Carlos Eduardo Jacob University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Fabricio L'ofreddo D'Ottaviano University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Conrado Alvarenga University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Adriana Safatle Ribeiro University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Ulysses Ribeiro Jr. University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Cláudio José Caldas Bresciani University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Bruno Zilberstein University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • José Eduardo Krieger University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Angelita Habr-Gama University of São Paulo; Faculty of Medicine; Hospital das Clínicas
  • Joaquim José Gama-Rodrigues University of São Paulo; Faculty of Medicine; Hospital das Clínicas

DOI:

https://doi.org/10.1590/S0041-87812004000500010

Keywords:

Gastric cancer, Genetics, Microsatellite instability

Abstract

Recently, the presence of microsatellite instability (MSI) has been reported in gastric cancer and associated with older age of presentation, distal tumor location, early disease staging, and better overall prognosis. Different characteristics in presentation and in tumor behavior may be explained by different genetic alterations during carcinogenesis of gastric cancer. Identification of specific genetic pathways in gastric cancer may have direct impact on prognosis and selection of treatment strategies. PATIENTS AND METHODS: All 24 patients were treated by radical surgery. Fragments of normal and tumor tissues were extracted from the specimen and stored at -80ºC before DNA purification and extraction. PCR amplification utilizing microsatellite markers was performed. Tumors presenting PCR products of abnormal sizes were considered positive for microsatellite instability (MSI+). RESULTS: Five patients (21%) had tumors that were MSI+ in at least 1 marker. In the group of patients with Lauren's intestinal-type gastric carcinoma, 3 had tumors that were MSI+ (23%), while in the group of diffuse-type gastric cancer, 2 patients had tumors that were MSI+ (19%). The mean age of presentation and the male:female ratio was similar in both groups. Tumors that were MSI+ were more frequently located in proximal portion of the stomach compared to microsatellite-stable (MSS) tumors (40% vs. 16%). Although there was a trend of patients with MSI+ tumors towards a proximal gastric tumor location, early staging, and negative lymph node metastasis, there was no statistical significance compared to those with MSS tumors (P >;.1). Comparison of overall and disease-free survival between gastric tumors that were MSI+ and those that were MSS found no statistically significant differences (P >;.1). CONCLUSIONS: Microsatellite instability is a frequent event in gastric carcinogenesis and shows a trend towards distinct clinical and pathological characteristics of gastric cancer.

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Published

2004-01-01

Issue

Section

Original Research

How to Cite

Perez, R. O., Jacob, C. E., D'Ottaviano, F. L., Alvarenga, C., Ribeiro, A. S., Ribeiro Jr., U., Bresciani, C. J. C., Zilberstein, B., Krieger, J. E., Habr-Gama, A., & Gama-Rodrigues, J. J. (2004). Microsatellite instability in solitary and sporadic gastric cancer . Revista Do Hospital Das Clínicas, 59(5), 279-285. https://doi.org/10.1590/S0041-87812004000500010