研究目的
Detection of breast cancer (BC) metastasis at the early stage is important for the assessment of BC progression status.
研究成果
The combination of functional 18F-FDG-PET/MRI parameters and molecular determination of YY1 could represent a novel integrated approach to predict synchronous metastatic disease with more accuracy than 18F-FDG-PET/MRI alone.
研究不足
It was a retrospective study performed at a single institution with a relatively small number of patients, and recurrence was documented in very few subjects. Moreover, we were unable to analyze overall survival because there were no disease-related deaths among the study population. The ROI segmentation was performed automatically. A manual segmentation could provide more accurate data. The knowledge of the tumor status for each patient would allow a potential correlation between YY1 with the invasiveness of BC. A larger number of subjects with the same characteristics could improve data sensitivity and speci?city. The data could not be validated internally. An external validation of our ?ndings would allow us to generalize the results and discriminate YY1 trend in all BC subtypes.
1:Experimental Design and Method Selection:
The study combined imaging parameters from hybrid 18F-FDG-PET/MRI and the expression level of the transcriptional factor Yin Yang 1 (YY1) for the detection of early metastases.
2:Sample Selection and Data Sources:
The study enrolled suspected n = 217 BC patients that underwent 18F-FDG-PET/MRI scans. The analysis retrospectively included n = 55 subjects. n = 40 were BC patients and n = 15 imaging-negative female individuals were healthy subjects (HS).
3:List of Experimental Equipment and Materials:
Hybrid 18F-FDG-PET/MRI system (mMR Biograph; Siemens, Erlangen, Germany), Trizol solution (Life Technologies/Gibco, Italy), Histopaque-10771 (Sigma-Aldrich), phosphate-bu?ered saline (PBS) pH7.4 (Gibco; Life Technologies/Gibco, Italy).
4:4 (Gibco; Life Technologies/Gibco, Italy). Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: Peripheral blood mononuclear cells (PBMCs) and serum aliquots were isolated. RNA was obtained from PBMCs and YY1 expression level was evaluated by qRT-PCR. An ELISA was used to determine the amount of YY1 serum protein.
5:Data Analysis Methods:
Statistical comparison between subgroups was evaluated by Mann-Whitney U and Spearman’s tests.
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