Rao Jun, Wang Xing, Wan Xianghui, Chen Chao, Xiong Xiaopeng, Xiong Aihua, Yang Zhiqing, Chen Lanyu, Wang Ting, Mao Lihua, Jiang Chunling, Zeng Jiquan, Zheng Zhi
The Second Affiliated Hospital of Nanchang Medical College, Jiangxi Cancer Institute, Jiangxi Cancer Hospital, Nanchang 330029, Jiangxi Province, China.
The First Affiliated Hospital of Nanchang Medical College, Jiangxi Provincial People's Hospital, Nanchang 330006, Jiangxi Province, China.
J Proteome Res. 2025 Jan 3;24(1):356-367. doi: 10.1021/acs.jproteome.4c00902. Epub 2024 Dec 19.
The prevalence rate of colorectal cancer (CRC) has dramatically increased in recent decades. However, robust CRC biomarkers with therapeutic value for early diagnosis are still lacking. To comprehensively reveal the molecular characteristics of CRC development, we employed a multiomics strategy to investigate eight different types of CRC samples. Proteomic analysis revealed 2022 and 599 differentially expressed tissue proteins between CRC and control groups in CRC patients and CRC mice, respectively. In patients with colorectal precancerous lesions, 25 and 34 significantly changed proteins were found between patients and healthy controls in plasma and white blood cells, respectively. Notably, vesicle-associated membrane protein-associated protein A (VAPA) was found to be consistently and significantly decreased in most types of CRC samples, and its level was also significantly correlated with increased overall survival of CRC patients. Furthermore, 37 significantly enriched pathways in CRC were further validated via metabolomics analysis. Ten VAPA-related pathways were found to be significantly enriched in CRC samples, among which PI3K-Akt signaling, central carbon metabolism in cancer, cholesterol metabolism, and ABC transporter pathways were also enriched in the premalignant stage. Our study identified VAPA and its associated pathways as key regulators, suggesting their potential applications in the early diagnosis and prognosis of CRC.
近几十年来,结直肠癌(CRC)的患病率急剧上升。然而,仍缺乏对早期诊断具有治疗价值的强大的CRC生物标志物。为了全面揭示CRC发生发展的分子特征,我们采用多组学策略研究了八种不同类型的CRC样本。蛋白质组学分析分别揭示了CRC患者和CRC小鼠的CRC组与对照组之间有2022种和599种差异表达的组织蛋白。在结直肠癌前病变患者中,血浆和白细胞中分别发现患者与健康对照之间有25种和34种显著变化的蛋白质。值得注意的是,在大多数类型的CRC样本中发现囊泡相关膜蛋白相关蛋白A(VAPA)持续且显著降低,其水平也与CRC患者总生存期的延长显著相关。此外,通过代谢组学分析进一步验证了CRC中37条显著富集的通路。发现10条与VAPA相关的通路在CRC样本中显著富集,其中PI3K-Akt信号通路、癌症中的中心碳代谢、胆固醇代谢和ABC转运蛋白通路在癌前阶段也有富集。我们的研究确定VAPA及其相关通路为关键调节因子,表明它们在CRC早期诊断和预后中的潜在应用。