Literature DB >> 28475823

Down-regulated miRs specifically correlate with non-cardial gastric cancers and Lauren's classification system.

Laura Lorenzon1, Claudia Cippitelli2, Riccardo Avantifiori1, Stefania Uccini2, Deborah French2, Maria Rosaria Torrisi2, Danilo Ranieri2, Paolo Mercantini1, Valeria Canu3, Giovanni Blandino1, Marco Cavallini1.   

Abstract

BACKGROUND AND OBJECTIVES: Gastric cancers are usually characterized using Lauren's classification into intestinal and diffuse types. We previously documented the down-modulation of miR31, miR148a, miR204, and miR375 in gastric cancers. We aimed this manuscript to investigate these miRs with the end-points of diagnosis, Lauren's classification and prognosis.
METHODS: A total of 117 resected non-cardial adenocarcinomas were evaluated for miRs' expressions. The performance of miRs' expressions for cancer diagnosis was tested using ROC curves. Logistic regression was conducted with the end-point of Lauren's classification. Kaplan-Meier and Cox analyses were performed for OS, DFS, and DSS. miRs' targets were reviewed using PRISMA method and BCL-2 was further investigated in cell lines.
RESULTS: ROC curves documented that miRs' down-modulation was significant in differentiating cancer versus normal tissues. Diffuse type cancers were associated with female sex, young age, and miR375 higher expression. We confirmed BCL-2 as a miR204 target. However, survival analyses confirmed the pathologic criteria (advanced stages, LNR, and low LNH) as the significant variables correlated to worse prognosis.
CONCLUSIONS: The down-modulation of miR31, miR148a, miR204, and miR375 is significantly associated with non-cardial gastric cancers and miR375 is specifically linked to Lauren's classification. Nevertheless, standard pathological features display as the independent variables associated with worse prognosis.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  Lauren classification; gastric cancer; miR148a; miR204; miR31; miR375; non-cardial gastric cancer

Mesh:

Substances:

Year:  2017        PMID: 28475823     DOI: 10.1002/jso.24648

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  2 in total

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  2 in total

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