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通过低覆盖度全基因组测序分析检测到的染色体不稳定性可预测接受根治性膀胱切除术的膀胱癌患者的预后。

Chromosomal instability by low-coverage whole-genome sequencing assay predicts prognosis in bladder cancer patients underwent radical cystectomy.

作者信息

Ding Qi, Zhu Hailiang, Fan Bo, Wang Lisheng, Jin Xiaohua, Cao Cheng, Shi Ying, Fan Zhijiang, Tu Wenjian, Li Feng

机构信息

Department of Urology, The First People's Hospital of Changshu, The Changshu Hospital Affiliated to Soochow University, 1 Shuyuan Street, Changshu, 215500, China.

Department of Gastroenterology, The First People's Hospital of Changshu, The Changshu Hospital Affiliated to Soochow University, 1 Shuyuan Street, 215500, Changshu, China.

出版信息

BMC Med Genomics. 2025 Jun 5;18(1):103. doi: 10.1186/s12920-025-02172-x.

Abstract

PURPOSE

To investigate chromosomal instability (CIN) in tumor tissue from radical bladder resection and to evaluate whether it can be used as a biomarker for the molecular typing of (BC).

METHODS

DNA was extracted from formalin-fixed paraffin-embedded samples of 50 BC patients who were followed up to March 23 2023 using the Qiagen nucleic acid kits. We analyzed CIN in tumor of bladder by low-coverage whole genome sequencing (LC-WGS). Kaplan-Meier log-rank test was used to perform survival analysis. The association between variables and overall and progression-free survival was analyzed using the Cox proportional hazards model.

RESULTS

There were 44 genome segments with statistically significant changes in copy number. CIN was significantly correlated with tumor stage, lymph node metastasis, relapse and survival status. Patients with high CIN were found to have a worse survival, with a median overall survival (OS) of 15 months. In addition, patients with high CIN were more likely to relapse, with a median progression-free survival (PFS) of 7 months. Patients with low CIN showed better OS and PFS. However, there was no significant difference in OS and PFS between T2 and T3-T4 patients. Multivariate cox regression analysis showed that high CIN was an independent predictor of OS, and high CIN and muscle invasion were independent predictors of PFS. Furthermore, patients with abnormal copy number of a single chromosome also had a poor prognosis, with a median survival of 14-30 months for OS and 5-10 months for PFS, while negative patients had a better prognosis.

CONCLUSION

CIN was significantly correlated with tumor stage, lymph node metastasis, relapse and survival status of BC. Patients with high CIN or abnormal copy numbers of a single chromosome have a poor prognosis. CIN might be better than T stage in predicting the prognosis of patients with BC. Molecular typing of CIN can be used as an independent prognostic factor for BC.

摘要

目的

研究根治性膀胱切除术后肿瘤组织中的染色体不稳定性(CIN),并评估其是否可作为膀胱癌(BC)分子分型的生物标志物。

方法

使用Qiagen核酸试剂盒从50例BC患者的福尔马林固定石蜡包埋样本中提取DNA,这些患者随访至2023年3月23日。我们通过低覆盖度全基因组测序(LC-WGS)分析膀胱肿瘤中的CIN。采用Kaplan-Meier对数秩检验进行生存分析。使用Cox比例风险模型分析变量与总生存期和无进展生存期之间的关联。

结果

有44个基因组片段的拷贝数存在统计学显著变化。CIN与肿瘤分期、淋巴结转移、复发和生存状态显著相关。发现CIN高的患者生存较差,总生存期(OS)中位数为15个月。此外,CIN高的患者更易复发,无进展生存期(PFS)中位数为7个月。CIN低的患者显示出更好的OS和PFS。然而,T2和T3-T4期患者的OS和PFS无显著差异。多变量cox回归分析显示,高CIN是OS的独立预测因子,高CIN和肌肉浸润是PFS的独立预测因子。此外,单条染色体拷贝数异常的患者预后也较差,OS中位数为14 - 30个月,PFS中位数为5 - 10个月,而阴性患者预后较好。

结论

CIN与BC的肿瘤分期、淋巴结转移、复发和生存状态显著相关。CIN高或单条染色体拷贝数异常的患者预后较差。CIN在预测BC患者预后方面可能优于T分期。CIN的分子分型可作为BC的独立预后因素。

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