血管内皮生长因子在淋巴细胞性甲状腺炎患者甲状腺乳头状癌发病过程中的作用。

IF 2.5 Q3 ENDOCRINOLOGY & METABOLISM Minerva endocrinology Pub Date : 2023-12-01 Epub Date: 2022-07-01 DOI:10.23736/S2724-6507.22.03663-6
Nese E Gulcelik, Safak Akin, Kadriye Aydin, Cisel Aydin Mericoz, Yesim G Guler Tezel, Aydan Usman
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引用次数: 1

摘要

背景:血管内皮生长因子(VEGF血管内皮生长因子(VEGF)在自身免疫性慢性炎症和甲状腺乳头状癌(PTC)的发病机制中起着关键作用。我们假设,由于血管内皮生长因子在 PTC 和淋巴细胞性甲状腺炎(LT)中的表达都会增加,它可能会刺激 LT 患者的 PTC 的发展。为了评估这一点,我们对患有和未患有 LT 的 PTC 患者的肿瘤和邻近非肿瘤组织进行了检查:研究共纳入 50 名 PTC 患者(52.50±7.41 岁)和 17 名结节性甲状腺肿(NG)患者(50.47±10.38 岁)。根据是否存在 LT,PTC 患者被进一步分为两组。对所有患者的血管内皮生长因子进行免疫组化分析,并对 PTC 患者的肿瘤组织和邻近非肿瘤组织进行评估:结果:我们发现,PTC 患者的 VEGF 染色强度评分和标记甲状腺细胞的百分比明显高于 NG 患者(PC 结论:就我们所知,PTC 患者的 VEGF 染色强度评分和标记甲状腺细胞的百分比明显高于 NG 患者:据我们所知,我们的研究结果首次证明,有LT的PTC患者相邻非肿瘤组织中VEGF的表达高于无LT的患者,这表明在LT存在的情况下,VEGF的表达可能在PTC的进展中起作用。
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The role of vascular endothelial growth factor in the development of papillary thyroid carcinoma in patients with lymphocytic thyroiditis.

Background: Vascular endothelial growth factor (VEGF) plays a pivotal role in the pathogenesis of autoimmune chronic inflammatory conditions and papillary thyroid carcinoma (PTC). We hypothesized that, as VEGF expression is increased both in PTC and in lymphocytic thyroiditis (LT), it may stimulate the development of PTC in patients with LT. To evaluate this, we examined both tumor and adjacent non-tumoral tissues of PTC patients with and without LT.

Methods: A total of 50 patients with PTC (52.50±7.41 years) and 17 patients with nodular goiter (NG) (50.47±10.38 years) were included in the study. According to the presence of LT, patients with PTC were further divided into two groups. Immunohistochemical analyses of VEGF were conducted in all patients and for PTC patients, both tumor tissue and adjacent non-tumoral tissue were evaluated.

Results: The scores for intensity of staining and percentage of labeled thyrocytes for VEGF were found to be significantly higher in the PTC patients than in the NG patients (P<0.001, P<0.001, respectively). The tumor tissue revealed similar scores for PTC patients with LT and without LT. However, the scores in adjacent non-tumoral tissue were higher in PTC patients with LT than in patients without LT (P=0.004, P=0.01, respectively).

Conclusions: To the best of our knowledge, our results are the first to demonstrate that the expression of VEGF in adjacent non-tumoral tissue were higher in PTC patients with LT than in those without, which shows a possible role of VEGF expression in the progression of PTC in the presence of LT.

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