Distinct Mutational Profile of Lynch Syndrome Colorectal Cancers Diagnosed under Regular Colonoscopy Surveillance

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http://hdl.handle.net/10138/333561

Lähdeviite

Ahadova , A , Pfuderer , P L , Ahtiainen , M , Ballhausen , A , Bohaumilitzky , L , Kösegi , S , Müller , N , Tang , Y L , Kosmalla , K , Witt , J , Endris , V , Stenzinger , A , von Knebel Doeberitz , M , Bläker , H , Renkonen-Sinisalo , L , Lepistö , A , Böhm , J , Mecklin , J-P , Seppälä , T T & Kloor , M 2021 , ' Distinct Mutational Profile of Lynch Syndrome Colorectal Cancers Diagnosed under Regular Colonoscopy Surveillance ' , Journal of clinical medicine , vol. 10 , no. 11 , 2458 . https://doi.org/10.3390/jcm10112458

Julkaisun nimi: Distinct Mutational Profile of Lynch Syndrome Colorectal Cancers Diagnosed under Regular Colonoscopy Surveillance
Tekijä: Ahadova, Aysel; Pfuderer, Pauline Luise; Ahtiainen, Maarit; Ballhausen, Alexej; Bohaumilitzky, Lena; Kösegi, Svenja; Müller, Nico; Tang, Yee Lin; Kosmalla, Kosima; Witt, Johannes; Endris, Volker; Stenzinger, Albrecht; von Knebel Doeberitz, Magnus; Bläker, Hendrik; Renkonen-Sinisalo, Laura; Lepistö, Anna; Böhm, Jan; Mecklin, Jukka-Pekka; Seppälä, Toni T.; Kloor, Matthias
Tekijän organisaatio: Staff Services
HUS Abdominal Center
Department of Surgery
Genome-Scale Biology (GSB) Research Program
II kirurgian klinikka
Clinicum
Digital Precision Cancer Medicine (iCAN)
ATG - Applied Tumor Genomics
Päiväys: 2021-06
Kieli: eng
Sivumäärä: 17
Kuuluu julkaisusarjaan: Journal of clinical medicine
ISSN: 2077-0383
DOI-tunniste: https://doi.org/10.3390/jcm10112458
URI: http://hdl.handle.net/10138/333561
Tiivistelmä: Regular colonoscopy even with short intervals does not prevent all colorectal cancers (CRC) in Lynch syndrome (LS). In the present study, we asked whether cancers detected under regular colonoscopy surveillance (incident cancers) are phenotypically different from cancers detected at first colonoscopy (prevalent cancers). We analyzed clinical, histological, immunological and mutational characteristics, including panel sequencing and high-throughput coding microsatellite (cMS) analysis, in 28 incident and 67 prevalent LS CRCs (n total = 95). Incident cancers presented with lower UICC and T stage compared to prevalent cancers (p < 0.0005). The majority of incident cancers (21/28) were detected after previous colonoscopy without any pathological findings. On the molecular level, incident cancers presented with a significantly lower KRAS codon 12/13 (1/23, 4.3% vs. 11/21, 52%; p = 0.0005) and pathogenic TP53 mutation frequency (0/17, 0% vs. 7/21, 33.3%; p = 0.0108,) compared to prevalent cancers; 10/17 (58.8%) incident cancers harbored one or more truncating APC mutations, all showing mutational signatures of mismatch repair (MMR) deficiency. The proportion of MMR deficiency-related mutational events was significantly higher in incident compared to prevalent CRC (p = 0.018). In conclusion, our study identifies a set of features indicative of biological differences between incident and prevalent cancers in LS, which should further be monitored in prospective LS screening studies to guide towards optimized prevention protocols.
Avainsanat: CARCINOMAS
CLINICAL MANAGEMENT
DATABASE
GUIDELINES
HEREDITARY
Lynch syndrome
MICROSATELLITE INSTABILITY
MSH2
RISK
SCREENING INTERVAL
TUMORS
cancer prevention
carcinogenesis
colonoscopy screening
colorectal cancer
incident cancer
microsatellite instability
mismatch repair deficiency
mutational profiling
3126 Surgery, anesthesiology, intensive care, radiology
3121 General medicine, internal medicine and other clinical medicine
Vertaisarvioitu: Kyllä
Tekijänoikeustiedot: cc_by
Pääsyrajoitteet: openAccess
Rinnakkaistallennettu versio: publishedVersion


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