Evaluation of microsatellite instability in routine examinations of surgical samples

Context: Approximately 20%-30% of colon cancer cases have a hereditary basis. The genetic defect may involve mismatch repair (MMR) genes, which results in microsatellite instability (MSI). MMR-deficient colorectal cancer may occur due to germline mutation (Lynch syndrome) or be a sporadic one. A tum...

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Main Authors: Pawel Wlaszczuk (Author), Aleksandra Kuzbinska (Author), Zuzanna Dobrosz (Author), Piotr Palen (Author), Krzysztof Pawlicki (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2022-01-01T00:00:00Z.
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001 doaj_52aa7eb1cfee42d0aafd5cf64b5b21f1
042 |a dc 
100 1 0 |a Pawel Wlaszczuk  |e author 
700 1 0 |a Aleksandra Kuzbinska  |e author 
700 1 0 |a Zuzanna Dobrosz  |e author 
700 1 0 |a Piotr Palen  |e author 
700 1 0 |a Krzysztof Pawlicki  |e author 
245 0 0 |a Evaluation of microsatellite instability in routine examinations of surgical samples 
260 |b Wolters Kluwer Medknow Publications,   |c 2022-01-01T00:00:00Z. 
500 |a 0377-4929 
500 |a 10.4103/IJPM.IJPM_1398_20 
520 |a Context: Approximately 20%-30% of colon cancer cases have a hereditary basis. The genetic defect may involve mismatch repair (MMR) genes, which results in microsatellite instability (MSI). MMR-deficient colorectal cancer may occur due to germline mutation (Lynch syndrome) or be a sporadic one. A tumor's histological features, supported by a panel of immunohistochemistry stains, enables pathologists to assess the MMR status, which in turn has beneficial effects on clinical management. Aims: We aimed to show the relations between histopathological features identified during routine examinations and MMR genes' mutations. Methods and Material: We reviewed retrospectively the material of the Department of Pathology fulfilling the revised Bethesda Guidelines. Statistical Analysis Used: We used Chi-square test, Spearman test, and epidemiological analysis. Results: For the PMS2 gene, the positive predictive value (PPV) indicates that 91% of cases neither present any histological lesions nor have genetic abnormalities. The negative predictive value (NPV) indicates that only 50% of cases have both histological and genetic changes. For the MSH6 gene, the PPV indicates that 85% of tumors without specific histological features do not have genetic abnormalities. Conclusions: We advise universal staining for MLH1, MSH2, MSH6, and PMS2 in every newly diagnosed colon cancer, but due to costly analyses we suggest a protocol for the selection of cases for MMR examinations. 
546 |a EN 
690 |a colorectal carcinoma (crc) 
690 |a lynch syndrome (ls) 
690 |a microsatellite instability (msi) 
690 |a mismatch repair (mmr) 
690 |a Pathology 
690 |a RB1-214 
690 |a Microbiology 
690 |a QR1-502 
655 7 |a article  |2 local 
786 0 |n Indian Journal of Pathology and Microbiology, Vol 65, Iss 1, Pp 87-92 (2022) 
787 0 |n http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2022;volume=65;issue=1;spage=87;epage=92;aulast=Wlaszczuk 
787 0 |n https://doaj.org/toc/0377-4929 
856 4 1 |u https://doaj.org/article/52aa7eb1cfee42d0aafd5cf64b5b21f1  |z Connect to this object online.