沙特乳腺癌症患者PIK3CA、c-MET和c-KIT突变的表达及其临床意义

R. Nassir, G. Esheba, H. M. A. Elmoneim, Ahlam S. Altowairqi, G. Nouman
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引用次数: 0

摘要

目的:PIK3CA是癌症突变最常见的途径。PIK3CA/PPTEN通路作为分子治疗的可能靶点正在进行深入研究。PIK3CA/PPTEN通路的失调是对抗HER2治疗产生耐药性的重要机制。因此,我们旨在研究沙特人群中癌症患者的PIK3CA/PTEN。方法:应用PTEN免疫组织化学方法对98例患者进行检测。然后,我们应用下一代测序来确定与癌症发展相关的遗传变异及其与临床病理变量的相关性。结果:PTEN的表达与淋巴结转移(LNM)、肿瘤分期、淋巴管侵犯(LVI)和癌症三阴性(TNBC)显著相关。PIK3CA突变的发生率为33.3%,它与LNM、肿瘤分期和PTEN表达显著相关。在41.7%的病例中发现了c-MET突变,它与肿瘤分期和TNBC有关,而在20.8%的病例中检测到c-KIT突变,它仅与TNBC显著相关。PTEN阳性表达的患者总体生存率(OS)显著提高;相反,PIK3CA和c-MET患者的OS明显较差。结论:我们的研究证实了PIK3CA/PTEN通路在癌症患者中的重要性。PIK3CA和c-MET突变频率较高,与预后不良有关。c-MET和c-KIT基因在TNBC的发生中都具有重要作用。这些发现应该扩大到一个更大的群体研究,以改善临床结果和个性化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression and Clinical Significance of PIK3CA, c-MET and c-KIT Mutations in Saudi Breast Cancer Patients
Objective: PIK3CA is the most common pathway affected by mutations in breast cancer. PIK3CA/PTEN pathway is under intense investigation as a possible target for molecular therapy. Dysregulation PIK3CA/PTEN pathway is a substantial mechanism for the development of resistance to anti-HER2 therapy. Therefore, we aimed to study the PIK3CA/PTEN in breast cancer patients in Saudi population. Methods: We applied PTEN immunohistochemistry on 98 patients. Then, we applied next-generation sequencing to determine the genetic variations associated with the development of breast cancer and their correlations with clinicopathological variables. Results: PTEN expression was significantly correlated with lymph node metastasis (LNM), tumor stage, lymphovascular invasion (LVI) and triple negative breast cancer (TNBC). The prevalence of the PIK3CA mutation was 33.3% of cases and it was significantly associated with LNM, tumor stage, and with PTEN expression. c-MET mutation was identified in 41.7% of cases and it was associated with tumor stage and with TNBC, while c-KIT mutation was detected in 20.8% of cases, and it was significantly associated with TNBC only. Patients with positive PTEN expression had a significantly better overall survival (OS); on the contrary, patients with PIK3CA and c-MET had a significantly worse OS. Conclusion: Our study confirms the importance of PIK3CA/PTEN pathway in breast cancer patients. A high frequency of PIK3CA and c-MET mutations was detected and was associated with poor prognosis. Both c-MET and c-KIT genes have significant roles in developing TNBC. These findings should be expanded to a larger group study to improve the clinical outcomes and individualizing treatment.
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