Behmanesh Mohammad Amin, Rafiee Paniz, Eidikhosh Forough, Moridnia Abbas
Department of Histology, School of Medicine, Dezful University of Medical Sciences, Dezful, Iran.
Infectious and Tropical Diseases Research Center, Dezful University of Medical Sciences, Dezful, Iran.
Sci Rep. 2025 Aug 30;15(1):32003. doi: 10.1038/s41598-025-17399-y.
In 2020, colorectal cancer (CRC) had over 1.9 million new cases and around 0.9 million deaths, making it the third most common cancer and the second leading cause of cancer deaths globally. GNAS mutations have been found in several cancers, including colon cancer, particularly in codon 201, which activates cAMP signaling and may lead to metastasis. The study aimed to find the frequency of the GNAS c.602G > A (p.Arg201His) mutation in CRC and analyze the pathology of tumors with this mutation. We collected a total of 40 tissue samples. DNA was extracted and analyzed using the High-Resolution Melting method followed by sequencing. In this study, 40 CRC patients were examined, revealing GNAS heterozygous mutations in 14 cases. Among these, 6 were women and 8 were men. Most cases (9) were grade 1 tumors, with varying sizes: 3 patients had tumors larger than 5 cm, 6 had tumors between 3 and 5 cm, and 5 had tumors smaller than 3 cm. Lymphatic involvement was observed in 5 patients. This study found a significant link between tumor size and lymphatic involvement, vascular metastasis, and gender. This study found that the heterozygous GNAS c.602G > A (p.Arg201His) mutation was present in a significant number of patients with CRC. There was a notable association between tumor size and lymphatic involvement, tumor size and vascular metastasis, and tumor size and gender. These findings suggest that the mutation may contribute to tumor progression and aggressive behavior in CRC. Therefore, it is important to further investigate GNAS mutations, as they could serve as potential molecular markers for predicting disease progression and guiding therapeutic decisions in CRC patients.
2020年,结直肠癌(CRC)新增病例超过190万例,死亡病例约90万例,使其成为全球第三大常见癌症和第二大致癌死亡原因。已在包括结肠癌在内的多种癌症中发现GNAS突变,特别是在密码子201处,该突变激活cAMP信号传导并可能导致转移。本研究旨在确定CRC中GNAS c.602G>A(p.Arg201His)突变的频率,并分析具有该突变的肿瘤的病理学特征。我们共收集了40份组织样本。提取DNA并采用高分辨率熔解法进行分析,随后进行测序。在本研究中,对40例CRC患者进行了检查,发现14例存在GNAS杂合突变。其中,女性6例,男性8例。大多数病例(9例)为1级肿瘤,大小各异:3例患者的肿瘤大于5cm,6例患者的肿瘤在3至5cm之间,5例患者的肿瘤小于3cm。5例患者观察到有淋巴转移。本研究发现肿瘤大小与淋巴转移、血管转移和性别之间存在显著关联。本研究发现,相当数量的CRC患者存在GNAS c.602G>A(p.Arg201His)杂合突变。肿瘤大小与淋巴转移、肿瘤大小与血管转移以及肿瘤大小与性别之间存在显著关联。这些发现表明,该突变可能促进CRC的肿瘤进展和侵袭性。因此,进一步研究GNAS突变非常重要,因为它们可能作为预测CRC患者疾病进展和指导治疗决策的潜在分子标志物。