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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Wolters Kluwer Medknow Publications,
2022-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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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. |