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

Author:

El Agy Fatima1ORCID,Otmani Ihssane El1ORCID,Mazti Asmae2,Lahmidani Nada3,Oussaden Abdelmalek4,El Abkari Mohamed3,Benjelloun El Bachir4,Moukit Wadih5ORCID,El Bouhaddouti Hicham4,Toughrai Imane4,Hassani Karim Ibn Majdoub4,Maazaz Khalid4,Benbrahim Zineb6ORCID,Mellas Nawfal6,El Rhazi Karima7,Ouldim Karim8,El Bardai Sanae2,Adil Ibrahimi Sidhi9,Ait Taleb Khalid9,Bennis Sanae10,Laila Chbani2

Affiliation:

1. Medical Center of Biomedical and Translational Research, Hassan II University Hospital, Fez, Morocco

2. Department of Pathological Anatomy, Hassan II University Hospital, Fez, Morocco

3. Department of Gastroenterology, Hassan II University Hospital, Fez, Morocco

4. Department of Visceral Surgery, Hassan II University Hospital, Fez, Morocco

5. Department of Obstetrics and Gynecology, Military Training Hospital Mohammed V, Rabat, Morocco

6. Department of Oncology, Hassan II University Hospital, Fez, Morocco

7. Laboratory of Epidemiology, Faculty of Medicine and Pharmacy, Fez, Morocco

8. Department of Medical Genetics and Ontogenetic, Hassan II University Hospital, Fez, Morocco

9. Department of General Surgery, Hassan II University Hospital, Fez, Morocco

10. Biomedical and Translational Research Laboratory, Faculty of Medicine and Pharmacy, Morocco

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. 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. 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). 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.

Publisher

Hindawi Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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