MMR deficiency is frequent in colorectal carcinomas with diffuse SLFN11 immunostaining: clinicopathologic and molecular study of 31 cases identified among 3,300 tumors
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
PubMed
40105034
PubMed Central
PMC11920882
DOI
10.1002/2056-4538.70025
Knihovny.cz E-zdroje
- Klíčová slova
- DNA damaging agents, Lynch syndrome, SLFN11, colorectal cancer, mismatch repair proteins, mucinous carcinoma,
- MeSH
- dospělí MeSH
- jaderné proteiny * metabolismus MeSH
- karcinom * metabolismus patologie MeSH
- kolon * metabolismus patologie MeSH
- kolorektální nádory * metabolismus patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikrosatelitní nestabilita * MeSH
- nádorové biomarkery metabolismus MeSH
- oprava chybného párování bází DNA MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- jaderné proteiny * MeSH
- nádorové biomarkery MeSH
- SLFN11 protein, human MeSH Prohlížeč
Schlafen 11 (SLFN11), a regulator of cell fate following DNA injury, sensitizes tumor cells to DNA-damaging agents. Patients with SLFN11-positive tumors may benefit from DNA-damaging chemotherapies. SLFN11 has been studied in different types of cancer including colorectal carcinomas. However, colorectal carcinomas with diffuse positivity (expression in ≥80% of tumor cells) have not been meticulously characterized. SLFN11 immunostaining of tumor microarrays (TMAs) with 3,300 primary CRCs identified 65 (~2.0%) tumors with focal staining (<10% of tumor nuclei positive), 83 (~2.5%) with patchy (≥10% and <80%) and 51 (~1.5%) with diffuse (≥80%) SLFN11 positivity. The latter was confirmed on full sections from donor blocks in 31 (~1%) cases, which were further studied including evaluation of additional immunohistochemical markers, genotyping with targeted DNA sequencing, and assessment of microsatellite instability. SLFN11-positive carcinomas were mostly (21/31, 68%) right-sided tumors with a female predominance (21/31, 68%) and median age of 67 years. Eighteen of 31 (58%) contained areas of mucinous differentiation. Deficiency of mismatch repair proteins was detected in 65% (20/31) of SLFN11-positive carcinomas. Moreover, MLH1 (n = 2), MSH2, MSH6, and PMS2 germline mutations were identified in 25% (5/20) of patients with mismatch repair deficient tumors. BRAF p.V600E mutation was found in 45% (9/20) of mismatch repair deficient, but only 1 of 11 proficient tumors. Colorectal carcinomas with diffuse SLFN11 positivity were often mismatch repair deficient tumors with their typical clinical, morphological, and molecular characteristics.
Bioptical Laboratory Ltd Plzen Czech Republic
Department of Clinical and Experimental Pathology Wrocław Medical University Wrocław Poland
Department of Molecular Diagnostics Holycross Cancer Center Kielce Poland
Laboratory of Pathology National Cancer Institute Bethesda MD USA
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