Microsatellite instability in colorectal cancer: Improved assessment using fluorescent polymerase chain reaction

1995 ◽  
Vol 109 (2) ◽  
pp. 465-471 ◽  
Author(s):  
Lynn Cawkwell ◽  
Ding Li ◽  
Fraser A. Lewis ◽  
Iain Martin ◽  
Michael F. Dixon ◽  
...  
2002 ◽  
Vol 126 (2) ◽  
pp. 202-204 ◽  
Author(s):  
Joerg Trojan ◽  
Jochen Raedle ◽  
Guenter Herrmann ◽  
Angela Brieger ◽  
Stefan Zeuzem

Abstract Microsatellite instability (MSI) is characteristic of hereditary nonpolyposis colorectal cancer (HNPCC). Owing to early onset of colorectal cancer before the age of 50 years and/or familial clustering of HNPCC-related malignancies, the diagnosis of HNPCC was suspected in 2 patients. Because no paraffin-embedded tumor tissue was available, we used archival 5-μm, hematoxylin-eosin–stained tumor specimen slides for direct MSI analysis. Tissue was microdissected and cells were lysed using 1% Triton. Fluorescence polymerase chain reaction amplification of a panel of 7 microsatellite markers, including all markers of the current international reference panel (BAT-25, BAT-26, D2S123, D5S346, and D17S250), demonstrated MSI in one patient and excluded MSI in the other. In conclusion, this study demonstrates the feasibility of MSI analysis by direct fluorescence polymerase chain reaction amplification using hematoxylin-eosin–stained tissue specimens without the need for prior DNA extraction.


Cells ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1401
Author(s):  
James Wei Tatt Toh ◽  
Puneet Singh ◽  
Venkata A. A. S. K. Tangirala ◽  
Alex Limmer ◽  
Kevin J. Spring

Background: Microsatellite instability (MSI) testing is important for the classification of Lynch syndrome, as a prognostic marker and as a guide for adjuvant chemotherapy in colorectal cancer (CRC). The gold standard for determining MSI status has traditionally been fluorescent multiplex polymerase chain reaction (PCR) and capillary gel electrophoresis (CGE). However, its use in the clinical setting has diminished and has been replaced by immunohistochemical (IHC) detection of loss of mismatch repair protein expression due to practicability and cost. The aim of this study was to develop a simple, cost-effective and accurate MSI assay based on CGE. Method: After amplification of microsatellites by polymerase chain reaction (PCR) using the National Cancer Institute (NCI) panel (BAT 25, BAT26, D5S346, D2S123, D17S250) of MSI markers, parallel CGE was utilized to classify colorectal cancers as MSI-H, MSI-L and MSS using the 5200 Fragment Analyzer System. Cell lines and patient cancer specimens were tested. DNA from 56 formalin-fixed paraffin-embedded cancer specimens and matched normal tissue were extracted and CGE was performed. An automated computational algorithm for MSI status determination was also developed. Results: Using the fragment analyser, MSI status was found to be 100% concordant with the known MSI status of cell lines and was 86% and 87% concordant with immunohistochemistry (IHC) from patient cancer specimens using traditional assessment and our MSI scoring system, respectively, for MSI determination. The misclassification rate was mainly attributed to IHC, with only one (1.8%) sampling error attributed to CGE testing. CGE was also able to distinguish MSI-L from MSI-H and MSS, which is not possible with IHC. An MSI score based on total allelic variability that can accurately determine MSI status was also successfully developed. A significant reduction in cost compared with traditional fluorescent multiplex PCR and CGE was achieved with this technique. Conclusions: A simple, cost-effective and reliable method of determining MSI status and an MSI scoring system based on an automatic computational algorithm to determine MSI status, as well as degree of allelic instability in colorectal cancer, has been developed using the 5200 Fragment Analyzer System.


2003 ◽  
Vol 23 (4) ◽  
pp. 287-291 ◽  
Author(s):  
J�r�me Solassol ◽  
Ha�ssam Rahil ◽  
Vincent Sapin ◽  
Didier Lemery ◽  
Bernard Dastugue ◽  
...  

2017 ◽  
Vol 07 (08) ◽  
Author(s):  
Cao Thi Tai Nguyen ◽  
Nguyen Trung Kien ◽  
Vu Thi Nhuan ◽  
Nguyen Dac Khoa ◽  
Nguyen Chung Vieng ◽  
...  

1999 ◽  
Vol 279 (1-2) ◽  
pp. 15-23 ◽  
Author(s):  
Moritoshi Kinoshita ◽  
Joshi Nakamura ◽  
Hiroko Kusaka ◽  
Toru Hadama ◽  
Kyoko Bago ◽  
...  

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