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Kansikas, Minttu; Vähätalo, Laura; Kantelinen, Jukka; Kasela, Mariann; Putula, Jaana; Døhlen, Anni; Paloviita, Pauliina; Kärkkäinen, Emmi; Lahti, Niklas; Arnez, Philippe; Kilpinen, Sami; Alcala-Repo, Beatriz; Pylvänäinen, Kirsi; Pöyhönen, Minna; Peltomäki, Päivi; Järvinen, Heikki J.; Seppälä, Toni T.; Renkonen-Sinisalo, Laura; Lepistö, Anna; Mecklin, Jukka-Pekka; Nyström, Minna

Tumor-independent Detection of Inherited Mismatch Repair Deficiency for the Diagnosis of Lynch Syndrome with High Specificity and Sensitivity

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  • Media type: E-Article
  • Title: Tumor-independent Detection of Inherited Mismatch Repair Deficiency for the Diagnosis of Lynch Syndrome with High Specificity and Sensitivity
  • Contributor: Kansikas, Minttu; Vähätalo, Laura; Kantelinen, Jukka; Kasela, Mariann; Putula, Jaana; Døhlen, Anni; Paloviita, Pauliina; Kärkkäinen, Emmi; Lahti, Niklas; Arnez, Philippe; Kilpinen, Sami; Alcala-Repo, Beatriz; Pylvänäinen, Kirsi; Pöyhönen, Minna; Peltomäki, Päivi; Järvinen, Heikki J.; Seppälä, Toni T.; Renkonen-Sinisalo, Laura; Lepistö, Anna; Mecklin, Jukka-Pekka; Nyström, Minna
  • Published: American Association for Cancer Research (AACR), 2023
  • Published in: Cancer Research Communications, 3 (2023) 3, Seite 361-370
  • Language: English
  • DOI: 10.1158/2767-9764.crc-22-0384
  • ISSN: 2767-9764
  • Origination:
  • Footnote:
  • Description: Lynch syndrome (LS) is the most common hereditary cancer syndrome. Early diagnosis improves prognosis and reduces health care costs, through existing cancer surveillance methods. The problem is finding and diagnosing the cancer predisposing genetic condition. The current workup involves a complex array of tests that combines family cancer history and clinical phenotypes with tumor characteristics and sequencing data, followed by a challenging task to interpret the found variant(s). On the basis of the knowledge that an inherited mismatch repair (MMR) deficiency is a hallmark of LS, we have developed and validated a functional MMR test, DiagMMR, that detects inherited MMR deficiency directly from healthy tissue without need of tumor and variant information. The validation included 119 skin biopsies collected from clinically pathogenic MMR variant carriers (MSH2, MSH6) and controls, and was followed by a small clinical pilot study. The repair reaction was performed on proteins extracted from primary fibroblasts and the interpretation was based on the MMR capability of the sample in relation to cutoff, which distinguishes MMR proficient (non-LS) from MMR deficient (LS) function. The results were compared with the reference standard (germline NGS). The test was shown to have exceptional specificity (100%) with high sensitivity (89%) and accuracy (97%). The ability to efficiently distinguish LS carriers from controls was further shown with a high area under the receiving operating characteristic (AUROC) value (0.97). This test offers an excellent tool for detecting inherited MMR deficiency linked to MSH2 or MSH6 and can be used alone or with conventional tests to recognize genetically predisposed individuals.Significance:Clinical validation of DiagMMR shows high accuracy in distinguishing individuals with hereditary MSH2 or MSH6 MMR deficiency (i.e., LS). The method presented overcomes challenges faced by the complexity of current methods and can be used alone or with conventional tests to improve the ability to recognize genetically predisposed individuals.
  • Access State: Open Access