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Methylation of SOX17 Gene in Plasma Circulating DNA and Its Correlation with Disease Status and Prognosis in Patients with Papillary Thyroid Carcinoma |
CHAO Xiangsong, SUN Jiabin, HOU Yinglong |
Jiamusi Central Hospital, Heilongjiang Jiamusi 154002, China |
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Abstract Objective: To explore the relationship between SOX17 gene methylation in plasma circulating DNA and the disease condition and prognosis of patients with papillary thyroid carcinoma (PTC). Methods: Thyroid cancer tissue and preoperative blood samples were collected from 152 PTC patients who underwent surgical resection between June 2022 and December 2023. Methylation-specific PCR (MSP) was used to detect SOX17 promoter methylation in PTC tissues and plasma circulating DNA. Results: MSP results showed that 71 out of 152 PTC tissue samples (46.7%) and 76 plasma circulating DNA samples (50.0%) exhibited SOX17 methylation. Spearman correlation analysis indicated a significant correlation between SOX17 methylation in plasma circulating DNA and PTC tissues (r=0.382, P<0.001). SOX17 methylation in PTC tissue and plasma circulating DNA was significantly associated with tumor stages Ⅱ~Ⅲ, tumor size ≥2cm, and lymph node metastasis (LNM) (P<0.05). Furthermore, SOX17 methylation in plasma circulating DNA was significantly related to the occurrence of extrathyroidal extension (ETE) (P<0.05). SOX17 methylation in plasma circulating DNA was identified as an independent factor influencing LNM and ETE in PTC patients (OR=9.564, 2.744; 95% CI=3.875~23.602, 1.109~6.792, P<0.05). The predictive ability of SOX17 methylation in plasma circulating DNA for LNM and ETE was relatively high, with an area under the curve (AUC) of 0.731 and 0.630 (sensitivity 74.0%, 65.6%; specificity 72.2%, 60.4%). In contrast, the predictive ability of SOX17 methylation in PTC tissues for LNM and ETE was lower, with an AUC of 0.604 and 0.562 (sensitivity 57.5%, 54.1%; specificity 63.3%, 58.2%). Conclusion: SOX17 promoter methylation in tumor tissue and plasma DNA exhibits high consistency during the occurrence and progression of PTC. Moreover, SOX17 promoter methylation in plasma DNA has a higher predictive value for LNM and ETE.
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