Zhang Wan-Ning, Liang Wei-Jie, Zhang Ying, Liang Ming-Jian, Zhang Ming-Juan, Chen Qi, Mo Zhou-Pei, Wu Mei-Yi, Weng Xue-Zi, Han Rui, Liang Yong-Neng, Ke Miao-La, Lin Wen-Qian
State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.
Department of Laboratory Medicine, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, 510180, China.
Heliyon. 2024 Jul 6;10(13):e34220. doi: 10.1016/j.heliyon.2024.e34220. eCollection 2024 Jul 15.
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.
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.
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.
Our study revealed genomic changes in SRCC patients across different blood groups, which could advance the understanding and precise treatment of colorectal SRCC.
结直肠印戒细胞癌(SRCC)是恶性腺癌的一种罕见亚型,约占结直肠癌(CRC)病例的1%。其生物标志物和分子特征仍存在争议,临床治疗尚无特异性治疗靶点或策略。
进行一项回顾性研究,研究时间为2010年1月至2021年12月。纳入分析的有来自中山大学肿瘤防治中心的1058例结直肠癌病例和来自肿瘤基因组图谱计划的489例病例,其中64例为SRCC。数据提取包括患者人口统计学、血型和危险因素,包括临床变量和基因组学(19基因panel NGS或1021基因panel NGS)。进行单因素分析以确定与总生存显著相关的因素。
27例(42.2%)、18例(28.1%)、12例(18.8%)和7例(10.9%)患者的血型分别为O型、A型、B型和AB型。我们发现O型是一种独特的血型,其特征为KRAS突变频率低、每个HLA I类位点杂合性频率高以及肿瘤突变负荷(TMB)高。具有高频KRAS突变的A型血患者和患有贫血及代谢异常的B型血患者需要靶向治疗。此外,SRCC的基因改变与腺癌和黏液腺癌不同。
我们的研究揭示了不同血型SRCC患者的基因组变化,这可能会促进对结直肠SRCC的理解和精准治疗。