SATB2 和 CDX2 的表达缺失与结直肠癌中 DNA 错配修复蛋白缺乏和 BRAF 基因突变有关。

IF 1.2 4区 医学 Q3 PATHOLOGY Medical Molecular Morphology Pub Date : 2024-03-01 Epub Date: 2023-08-15 DOI:10.1007/s00795-023-00366-9
Jiezhen Li, Qiang Zeng, Jie Lin, Haijian Huang, Lingfeng Chen
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引用次数: 0

摘要

SATB2和CDX2蛋白的表达与结直肠癌(CRC)常见的分子改变和临床预后之间的关系仍有待进一步明确。我们收集了 1180 例 CRC 病例,并使用全切片免疫组化技术探讨了 SATB2 和 CDX2 的表达与 CRC 的临床病理特征、分子改变和总生存期之间的关系。我们的研究结果表明,SATB2和CDX2的阴性表达在MMR蛋白缺陷型CRC中比在MMR蛋白完善型CRC中更常见(分别为15.8% vs. 6.0%,P = 0.001;14.5% vs. 4.0%,P = 0.000)。与 BRAF 野生型 CRC 相比,SATB2 和 CDX2 的负表达在 BRAF 突变型 CRC 中更为常见(分别为 17.2% vs. 6.1%,P = 0.003;13.8% vs. 4.2%,P = 0.004)。SATB2和/或CDX2阴性表达与KRAS、NRAS和PIK3CA突变之间没有关系。SATB2和CDX2的不表达与CRC的不良组织病理学特征有关。在多变量分析中,SATB2 阴性表达(P = 0.030)、CDX2 阴性表达(P = 0.043)和晚期临床分期(P = 0.000)与 CRC 总生存率下降有关。总之,SATB2和CDX2在CRC中的缺失与MMR蛋白缺乏和BRAF突变有关,但与KRAS、NRAS和PIK3CA突变无关。SATB2和CDX2是CRC患者的预后生物标志物。
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Loss of SATB2 and CDX2 expression is associated with DNA mismatch repair protein deficiency and BRAF mutation in colorectal cancer.

The relationship between the expression of the SATB2 and CDX2 proteins and common molecular changes and clinical prognosis in colorectal cancer (CRC) still needs further clarification. We collected 1180 cases of CRC and explored the association between the expression of SATB2 and CDX2 and clinicopathological characteristics, molecular alterations, and overall survival of CRC using whole-slide immunohistochemistry. Our results showed that negative expression of SATB2 and CDX2 was more common in MMR-protein-deficient CRC than in MMR-protein-proficient CRC (15.8% vs. 6.0%, P = 0.001; 14.5% vs. 4.0%, P = 0.000, respectively). Negative expression of SATB2 and CDX2 was more common in BRAF-mutant CRC than in BRAF wild-type CRC (17.2% vs. 6.1%, P = 0.003; 13.8% vs. 4. 2%; P = 0.004, respectively). There was no relationship between SATB2 and/or CDX2 negative expression and KRAS, NRAS, and PIK3CA mutations. The lack of expression of SATB2 and CDX2 was associated with poor histopathological features of CRC. In multivariate analysis, negative expression of SATB2 (P = 0.030), negative expression of CDX2 (P = 0.043) and late clinical stage (P = 0.000) were associated with decreased overall survival of CRC. In conclusion, the lack of SATB2 and CDX2 expression in CRC was associated with MMR protein deficiency and BRAF mutation, but not with KRAS, NRAS and PIK3CA mutation. SATB2 and CDX2 are prognostic biomarkers in patients with CRC.

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来源期刊
Medical Molecular Morphology
Medical Molecular Morphology 医学-病理学
CiteScore
2.90
自引率
5.60%
发文量
30
审稿时长
>12 weeks
期刊介绍: Medical Molecular Morphology is an international forum for researchers in both basic and clinical medicine to present and discuss new research on the structural mechanisms and the processes of health and disease at the molecular level. The structures of molecules, organelles, cells, tissues, and organs determine their normal function. Disease is thus best understood in terms of structural changes in these different levels of biological organization, especially in molecules and molecular interactions as well as the cellular localization of chemical components. Medical Molecular Morphology welcomes articles on basic or clinical research in the fields of cell biology, molecular biology, and medical, veterinary, and dental sciences using techniques for structural research such as electron microscopy, confocal laser scanning microscopy, enzyme histochemistry, immunohistochemistry, radioautography, X-ray microanalysis, and in situ hybridization. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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