Liu Xin, Zhang Sheng, Qiu Hao, Xie Zhi-Qiang, Tang Wei-Feng, Chen Yu, Wei Xi
Department of General Surgery, Changzhou Third People's Hospital, Changzhou 213001, Jiangsu Province, China.
Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang 212000, Jiangsu Province, China.
World J Gastrointest Oncol. 2025 Apr 15;17(4):102584. doi: 10.4251/wjgo.v17.i4.102584.
Accumulating studies indicated that maintain nuclei homeostasis was deemed to the protective factors for the occurrence of cancer. Thus, high-mobility group box 1 (HMGB1) might influence the risk and poorer prognoses of colorectal cancer (CRC).
This study was designed to investigate whether HMGB1 polymorphisms influence the risk and lymph node metastasis (LNM) of CRC.
Firstly, we designed an investigation with 1003 CRC patients and 1303 cancer-free controls to observe whether HMGB1 rs1412125 T > C and rs1045411 C > T SNPs could influence the risk of cancer. Subsequently, we carried out a correlation-analysis to assess whether these SNPs could alter the risk of LNM.
The current investigation suggested a relationship of HMGB1 rs1412125 SNP with the increased susceptibility of CRC. In a subgroup analysis, our findings suggested that this SNP could enhance an occurrence of CRC in ≥ 61 years, non-drinker and body mass index < 24 kg/m subgroups However, we found that there was null association between HMGB1 rs1412125 SNP and LNM, even in different CRC region. These observations were confirmed by calculating the power value (more than 0.8). The association of HMGB1 rs1045411 C > T SNP with CRC risk and LNM was not found in any compare.
This study highlights a possible association between HMGB1 rs1412125 polymorphism and the increased risk of CRC. In the future, more studies should be conducted to explore HMGB1 rs1412125 polymorphism in relation to CRC development.
越来越多的研究表明,维持细胞核稳态被认为是癌症发生的保护因素。因此,高迁移率族蛋白B1(HMGB1)可能影响结直肠癌(CRC)的发病风险和较差的预后。
本研究旨在探讨HMGB1基因多态性是否影响CRC的发病风险和淋巴结转移(LNM)。
首先,我们设计了一项针对1003例CRC患者和1303例无癌对照的调查,以观察HMGB1 rs1412125 T>C和rs1045411 C>T单核苷酸多态性(SNP)是否会影响癌症风险。随后,我们进行了相关性分析,以评估这些SNP是否会改变LNM的风险。
目前的调查表明,HMGB1 rs1412125 SNP与CRC易感性增加之间存在关联。在亚组分析中,我们的研究结果表明,该SNP可增加61岁及以上、不饮酒且体重指数<24 kg/m²亚组中CRC的发生率。然而,我们发现,即使在不同的CRC区域,HMGB1 rs1412125 SNP与LNM之间也无关联。通过计算检验效能值(大于0.8)证实了这些观察结果。在任何比较中均未发现HMGB1 rs1045411 C>T SNP与CRC风险和LNM之间存在关联。
本研究强调了HMGB1 rs1412125多态性与CRC风险增加之间可能存在关联。未来,应开展更多研究以探索HMGB1 rs1412125多态性与CRC发生发展的关系。