Radiotherapy Response in Microsatellite Instability Related Rectal Cancer.
- Author:
Joo Shik SHIN
1
;
Thein Ga TUT
;
Tao YANG
;
C Soon LEE
Author Information
1. Discipline of Pathology, University of Western Sydney School of Medicine, Liverpool, NSW, Australia. j.shin@uws.edu.au
- Publication Type:Review
- Keywords:
Rectal neoplasms;
Radiotherapy sensitivity;
Microsatellite instability;
DNA damage response;
DNA mismatch repair
- MeSH:
Apoptosis;
Cell Cycle Checkpoints;
Colorectal Neoplasms;
DNA;
DNA Damage;
DNA Mismatch Repair;
Humans;
Microsatellite Instability;
Microsatellite Repeats;
Proteins;
Radiation Injuries;
Radiation Tolerance;
Rectal Neoplasms;
Succinimides
- From:Korean Journal of Pathology
2013;47(1):1-8
- CountryRepublic of Korea
- Language:English
-
Abstract:
Preoperative radiotherapy may improve the resectability and subsequent local control of rectal cancers. However, the extent of radiation induced regression in these tumours varies widely between individuals. To date no reliable predictive marker of radiation sensitivity in rectal cancer has been identified. At the cellular level, radiation injury initiates a complex molecular network of DNA damage response (DDR) pathways that leads to cell cycle arrest, attempts at re-constituting the damaged DNA and should this fail, then apoptosis. This review presents the details which suggest the roles of DNA mismatch repair proteins, the lack of which define a distinct subset of colorectal cancers with microsatellite instability (MSI), in the DDR pathways. Hence routine assessment of the MSI status in rectal cancers may potentially serve as a predictor of radiotherapy response, thereby improving patient stratification in the administration of this otherwise toxic treatment.
