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首页> 外文期刊>Journal of Translational Medicine >Mass spectrometry-based analysis of therapy-related changes in serum proteome patterns of patients with early-stage breast cancer
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Mass spectrometry-based analysis of therapy-related changes in serum proteome patterns of patients with early-stage breast cancer

机译:基于质谱的早期乳腺癌患者血清蛋白质组模式治疗相关变化的分析

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Background The proteomics approach termed proteome pattern analysis has been shown previously to have potential in the detection and classification of breast cancer. Here we aimed to identify changes in serum proteome patterns related to therapy of breast cancer patients. Methods Blood samples were collected before the start of therapy, after the surgical resection of tumors and one year after the end of therapy in a group of 70 patients diagnosed at early stages of the disease. Patients were treated with surgery either independently (26) or in combination with neoadjuvant chemotherapy (5) or adjuvant radio/chemotherapy (39). The low-molecular-weight fraction of serum proteome was examined using MALDI-ToF mass spectrometry, and then changes in intensities of peptide ions registered in a mass range between 2,000 and 14,000 Da were identified and correlated with clinical data. Results We found that surgical resection of tumors did not have an immediate effect on the mass profiles of the serum proteome. On the other hand, significant long-term effects were observed in serum proteome patterns one year after the end of basic treatment (we found that about 20 peptides exhibited significant changes in their abundances). Moreover, the significant differences were found primarily in the subgroup of patients treated with adjuvant therapy, but not in the subgroup subjected only to surgery. This suggests that the observed changes reflect overall responses of the patients to the toxic effects of adjuvant radio/chemotherapy. In line with this hypothesis we detected two serum peptides (registered m/z values 2,184 and 5,403 Da) whose changes correlated significantly with the type of treatment employed (their abundances decreased after adjuvant therapy, but increased in patients treated only with surgery). On the other hand, no significant correlation was found between changes in the abundance of any spectral component or clinical features of patients, including staging and grading of tumors. Conclusions The study establishes a high potential of MALDI-ToF-based analyses for the detection of dynamic changes in the serum proteome related to therapy of breast cancer patients, which revealed the potential applicability of serum proteome patterns analyses in monitoring the toxicity of therapy.
机译:背景技术蛋白质组学方法被称为蛋白质组模式分析,先前已被证明在乳腺癌的检测和分类中具有潜力。在这里,我们旨在确定与乳腺癌患者治疗相关的血清蛋白质组模式的变化。方法在70例早期诊断为疾病的患者中,从治疗开始前,手术切除肿瘤后和治疗结束后一年采集血液样本。患者分别接受手术治疗(26)或与新辅助化疗(5)或辅助放疗/化学疗法(39)结合使用。使用MALDI-ToF质谱法检查了血清蛋白质组的低分子量部分,然后鉴定了在2,000和14,000 Da之间的质量范围内记录的肽离子强度变化,并将其与临床数据相关联。结果我们发现手术切除肿瘤对血清蛋白质组的质量分布没有立即的影响。另一方面,在基础治疗结束一年后,血清蛋白质组模式观察到了显着的长期影响(我们发现约20种肽的丰度发生了显着变化)。此外,显着差异主要在辅助治疗的患者亚组中发现,而在仅接受手术治疗的亚组中则没有。这表明观察到的变化反映了患者对辅助放射/化学疗法毒性作用的总体反应。根据这一假设,我们检测到了两种血清肽(m / z值分别为2,184和5,403 Da),其变化与所用治疗类型显着相关(辅助治疗后其丰度降低,而仅接受手术治疗的患者其丰度降低)。另一方面,在患者的任何频谱成分的丰度变化或临床特征(包括肿瘤的分期和等级)之间均未发现显着相关性。结论该研究为检测与乳腺癌患者治疗有关的血清蛋白质组动态变化建立了基于MALDI-ToF的分析方法,具有很高的潜力,这揭示了血清蛋白质组模式分析在监测治疗毒性方面的潜在适用性。

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