Biased expression of mutant alleles in cancer-related genes in esophageal squamous cell carcinoma

• Published in: Esophagus : official journal of the Japan Esophageal Society 2022-04, Vol.19 (2), p.294-302
• Main Authors: Takahashi, Masahiko, Hosomichi, Kazuyoshi, Nakaoka, Hirofumi, Sakata, Haruhito, Uesato, Naoya, Murakami, Kentaro, Kano, Masayuki, Toyozumi, Takeshi, Matsumoto, Yasunori, Isozaki, Tetsuro, Sekino, Nobufumi, Otsuka, Ryota, Inoue, Itsuro, Matsubara, Hisahiro
• Format: Article
• Language: English
• Subjects: Alleles; Cell cycle; Esophageal cancer; Esophageal Neoplasms - genetics; Esophageal Squamous Cell Carcinoma - genetics; Gastroenterology; Humans; Medicine; Medicine & Public Health; Mutation; Original Article; Pathogenesis; Squamous cell carcinoma; Surgical Oncology; Thoracic Surgery; Transcription Factors - genetics; Tumor Suppressor Protein p53 - genetics; Tumor Suppressor Proteins - genetics
• ISSN: 1612-9059; 1612-9067
• DOI: 10.1007/s10388-021-00900-7

Background Recent progress of large-scale international studies has provided comprehensive catalogs of somatic mutations in cancers. Additionally, it has become evident that allelic imbalance in the abundance of somatic mutations between DNA and RNA were pervasive in various types of cancer. However, the allelic imbalance of the abundance of somatic mutations in esophageal squamous cell carcinoma (ESCC) has not been fully analyzed. Methods We performed exome sequencing for 25 Japanese patients with ESCC to detect a comprehensive catalog of somatic mutations in ESCC. Additionally, we performed mRNA sequencing to evaluate the allelic imbalance of the identified somatic mutations at the transcriptional level by comparing the mutant allele frequencies between RNA and DNA. Results The exome sequencing showed that TP53 and ZNF750 were significantly mutated genes. The expression levels of TP53 and ZNF750 were different depending on the mutation status. In almost all the tumors with missense mutations in TP53 and ZNF750 , the mutant allele frequencies were higher in the RNA sequencing than those in the exome sequencing, indicating that the mutant alleles were preferentially expressed. By examining the allelic imbalances for all the identified missense mutations, we demonstrated that genes showing preferential expressions of the mutant alleles were involved in the pathways including cell cycle, cell death, and chromatin modification. Conclusions The results of this study suggest that the allelic imbalance of the abundance of somatic mutations plays important roles in the initiation and progression of ESCC by modulating cancer-related biological pathways.