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.

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

RANIERI, DANILO;
2017-01-01

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
Inglese
Inglese
116
2
184
194
11
Esperti anonimi
gastric cancer
lauren classification
mir148a
mir204
mir31
mir375
non-cardial gastric cancer
adenocarcinoma
adult
age factors
aged
aged
80 and over
cell line
tumor
down-regulation
female
gene expression regulation
neoplastic
humans
janus kinase 2
male
micrornas
middle aged
prognosis
protein-serine-threonine kinases
proto-oncogene proteins c-bcl-2
pyruvate dehydrogenase (acetyl-transferring) kinase
roc curve
repressor proteins
retrospective studies
sensitivity and specificity
sex factors
stomach neoplasms
11
info:eu-repo/semantics/article
262
Lorenzon, Laura; Cippitelli, Claudia; Avantifiori, Riccardo; Uccini, Stefania; French, Deborah; Torrisi, Maria Rosaria; Ranieri, Danilo; Mercantini, P...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14085/21589
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