Molecular characteristics of patients with colorectal signet-ring cell carcinoma with different ABO blood groups

被引:0
作者
Zhang, Wan-Ning [1 ]
Liang, Wei-Jie [2 ]
Zhang, Ying [1 ]
Liang, Ming-Jian [1 ]
Zhang, Ming-Juan [1 ]
Chen, Qi [1 ]
Mo, Zhou-Pei [1 ]
Wu, Mei-Yi [1 ]
Weng, Xue-Zi [1 ]
Han, Rui [1 ]
Liang, Yong-Neng [1 ]
Ke, Miao-La [1 ]
Lin, Wen-Qian [1 ]
机构
[1] Sun Yat Sen Univ, State Key Lab Oncol South China, Canc Ctr, Guangzhou 510060, Peoples R China
[2] South China Univ Technol, Guangzhou Peoples Hosp 1, Dept Lab Med, Guangzhou 510180, Peoples R China
关键词
Colorectal neoplasms; Carcinoma; Signet ring cell; ABO blood -group system; Mutation; HLA antigens; CANCER; RISK; ADENOCARCINOMA; RECTUM;
D O I
10.1016/j.heliyon.2024.e34220
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Colorectal signet-ring cell carcinoma (SRCC) is a rare subtype of malignant adenocarcinoma, accounting for approximately 1 % of colorectal cancer (CRC) cases. Its biomarkers and molecular characteristics remain controversial, and there are no specific therapeutic targets or strategies for its clinical treatment. Methods: A retrospective study was conducted between January 2010 and December 2021. 1058 colorectal cancer cases from the Sun Yat-sen University Cancer Center and 489 cases from the Tumor Genome Atlas Project were included in the analysis, of which 64 were SRCC. Data extraction included patient demographics, blood types and risk factors, including clinical variables and genomics (either a 19-gene panel NGS or 1021-gene panel NGS). Univariate analyses were performed to identify factors significantly associated with overall survival. Results: The blood groups of 27 (42.2 %), 18 (28.1 %), 12 (18.8 %), and seven (10.9 %) patients were classified as O, A, B, and AB, respectively. We found that O was a unique blood group characterized by a low frequency of KRAS mutations, a high frequency of heterozygosity at each HLA class I locus, and a high tumor mutational burden (TMB). Patients in blood group A with high-frequency KRAS mutations and those in blood group B with anemia and metabolic abnormalities required targeted treatment. Furthermore, genetic alterations in SRCC differed from those in adenocarcinoma and mucinous adenocarcinoma. Conclusions: Our study revealed genomic changes in SRCC patients across different blood groups, which could advance the understanding and precise treatment of colorectal SRCC.
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