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青海地区乳腺癌PIK3CA和TP53基因热点突变的病理特征分析

Pathological Characteristics of Hotspot Mutations in PIK3CA and TP53 Genes in Breast Cancer Cases from Qinghai Province

  • 摘要:
    目的 分析青海地区汉族、藏族及回族乳腺癌患者PIK3CA和TP53基因热点突变的民族差异及其与临床病理特征的关系,为少数民族乳腺癌的精准防治提供分子依据。
    方法 回顾性收集2022年6月—2023年5月青海大学附属医院382例乳腺癌手术患者癌组织样本(汉族200例、藏族93例、回族89例),通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)检测PIK3CA(E542K、H1047R、E545K)和TP53(R273H、R175H)突变,分析突变与临床病理参数的相关性。
    结果 三个民族乳腺癌的pTNM、淋巴结转移、分子分型和PR状态存在显著差异。PIK3CA和TP53的总体突变率为48.95%藏族PIK3CA-p.E542K突变率显著高于汉族和回族,PIK3CA-p.E545K变异检出率低于汉族。PIK3CA-p.E542K突变与淋巴结转移风险升高相关;TP53-p.R175H突变与pTNM晚期分期、脉管侵犯及三阴性乳腺癌显著相关;PIK3CA-H1047R和E545K突变富集于腔面A型。
    结论 青海多民族乳腺癌突变谱存在显著差异,藏族人群PIK3CA-p.E542K高频突变可能为区域特异性防治靶点。基因突变与肿瘤侵袭性及分子分型密切相关,检测PIK3CA/TP53突变可为高原地区乳腺癌早期风险分层和个体化治疗提供依据。

     

    Abstract:
    Objective To analyze ethnic differences in hotspot mutations of the PIK3CA and TP53 genes among breast cancer patients from the Han, Tibetan, and Hui ethnic groups in Qinghai, China, and their associations with clinicopathological characteristics.
    Methods A total of 382 breast cancer tissue samples were retrospectively collected from surgical patients (June 2022–May 2023), comprising 200 Han, 93 Tibetan, and 89 Hui ethnicity. Mutations in PIK3CA (E542K, H1047R, and E545K) and TP53 (R273H and R175H) were detected by using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Correlations between mutations and clinicopathological parameters were analyzed.
    Results Significant differences were observed in pTNM stage, lymph node metastasis, molecular subtypes, and PR status among the three ethnic groups. The overall mutation rate of PIK3CA and TP53 was 48.95%. The PIK3CA-p.E542K mutation rate in Tibetan cohort was significantly higher than those in Han and Hui cohort, whereas the detection rate of the PIK3CA-p.E545K mutation was lower in Tibetan cohort than that in Han cohort. The PIK3CA-p.E542K mutation was associated with an increased risk of lymph node metastasis. The TP53-p.R175H mutation was significantly correlated with advanced pTNM stage, vascular invasion, and triple-negative breast cancer. The PIK3CA-H1047R and E545K mutations were enriched in the luminal A subtype of breast cancer.
    Conclusion Considerable ethnic disparities exist in breast cancer mutation profiles in Qinghai, with the high-frequency PIK3CA-p.E542K mutation in Tibetan population potentially serving as a region-specific therapeutic target. Mutations are closely linked to tumor aggressiveness and molecular subtypes, highlighting the value of PIK3CA/TP53 mutation detection for early risk stratification and personalized treatment of breast cancer in high-altitude populations.

     

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