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Implication of Microsatellite Instability Pathway in Outcome of Colon Cancer in Moroccan Population.

Authors :
El Agy F
Otmani IE
Mazti A
Lahmidani N
Oussaden A
El Abkari M
Benjelloun EB
Moukit W
El Bouhaddouti H
Toughrai I
Hassani KM
Maazaz K
Benbrahim Z
Mellas N
El Rhazi K
Ouldim K
El Bardai S
Adil Ibrahimi S
Ait Taleb K
Bennis S
Laila C
Source :
Disease markers [Dis Markers] 2019 Dec 07; Vol. 2019, pp. 3210710. Date of Electronic Publication: 2019 Dec 07 (Print Publication: 2019).
Publication Year :
2019

Abstract

Background: Tumors with microsatellite instability (MSI tumors) have distinct clinicopathological features. However, the relation between these tumor subtypes and survival in colon cancer remains controversial. The aim of this study was to evaluate the overall survival (OS) in patients with MSI phenotype, in FES population.<br />Methods: The expression of MMR proteins was evaluated by immunohistochemistry for 330 patients. BRAF , KRAS , and NRAS mutations were examined by Sanger sequencing and pyrosequencing methods. The association of MSI status with a patient's survival was assessed by the Kaplan-Meier method and log-rank test.<br />Results: The mean age was 54.6 years (range of 19-90 years). The MSI status was found in 11.2% of our population. MSI tumors were significantly associated with male gender, younger patients, stage I-II, right localization, and a lower rate of lymph node and distant metastasis. The OS tends to be longer in MSI tumors than MSS tumors (109.71 versus 74.08), with a difference close to significance ( P = 0.05).<br />Conclusion: Our study demonstrates that MSI tumors have a particular clinicopathological features. The results of survival analysis indicate that the MSI status was not predictive of improved overall survival in our context with a lower statistical significance ( P = 0.05) after multivariate analysis.<br />Competing Interests: The authors report no conflicts of interest.<br /> (Copyright © 2019 Fatima El Agy et al.)

Details

Language :
English
ISSN :
1875-8630
Volume :
2019
Database :
MEDLINE
Journal :
Disease markers
Publication Type :
Academic Journal
Accession number :
31885734
Full Text :
https://doi.org/10.1155/2019/3210710