| Literature DB >> 35618879 |
Alberto Puccini1,2, Kelsey Poorman3, Fabio Catalano2, Andreas Seeber4, Richard M Goldberg5, Mohamed E Salem6, Anthony F Shields7, Martin D Berger1, Francesca Battaglin1, Ryuma Tokunaga1, Madiha Naseem1, Wu Zhang1, Philip A Philip7, John L Marshall8, W Michael Korn3, Heinz-Josef Lenz9.
Abstract
Signet ring cell carcinoma (SRCC) is rare: about 10% of gastric cancer (GC) and 1% of colorectal cancer (CRC). SRCC is associated with poor prognosis, however the underlying molecular characteristics are unknown. SRCCs were analyzed using NGS, immunohistochemistry, and in situ hybridization. Tumor mutational burden (TMB) was calculated based on somatic nonsynonymous missense mutations, and microsatellite instability (MSI) was evaluated by NGS of known MSI loci. A total of 8500 CRC and 1100 GC were screened. Seventy-six SRCC were identified from the CRC cohort (<1%) and 98 from the GC cohort (9%). The most frequently mutated genes in CRC-SRCC were TP53 (47%), ARID1A (26%), APC (25%); in GC-SRCC were TP53 (42%), ARID1A (27%), CDH1 (11%). When compared to non-SRCC histology (N = 3522), CRC-SRCC (N = 37) more frequently had mutations in BRCA1 (11% vs 1%, P < 0.001) and less frequently mutations in APC (19% vs 78%, P < 0.001), KRAS (22% vs 51%, P = 0.001) and TP53 (47% vs 73%, P = 0.001). Among the GC cohort, SRCC (N = 54) had a higher frequency of mutations in CDH1, BAP1, and ERBB2, compared to non-SRCC (N = 540). Our data suggest that SRCCs harbor a similar molecular profile, regardless of the tumor location. Tailored therapy may become available for these patients.Entities:
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Year: 2022 PMID: 35618879 PMCID: PMC9457205 DOI: 10.1038/s41388-022-02350-6
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 8.756