甲状腺乳头状癌合并桥本甲状腺炎肿瘤微环境相关趋化因子的临床意义
Clinical Significance of Tumor Microenvironment-related Chemokines in Papillary Thyroid Carcinoma Combined with Hashimoto"s Thyroiditis
投稿时间:2024-08-14  修订日期:2024-10-13
DOI:
中文关键词:  桥本甲状腺炎  甲状腺乳头状癌  趋化因子  免疫微环境
英文关键词:Hashimoto"s thyroiditis  Papillary Thyroid Carcinoma  Chemokines  Immune microenvironment
基金项目:国家自然科学基金项目(面上项目,重点项目,重大项目)
作者单位邮编
乔琳舒 杭州师范大学 311121
邵圣赞 浙江省人民医院 
戴 天 杭州师范大学 
吕 恬 浙江省人民医院 
葛明华* 浙江省人民医院 310014
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中文摘要:
      目的 :探讨甲状腺乳头状癌(Papillary Thyroid Carcinoma,PTC)合并桥本甲状腺炎(Hashimoto"s thyroiditis,HT)肿瘤微环境中相关趋化因子的临床意义。 方法:收集 2023年 5月-10月浙江省人民医院60例甲状腺乳头状癌患者病理组织切片,将其分为PTC with HT组、PTC without HT组、淋巴结转移(Lymph?Node?Metastases ,LNM) PTC with HT组以及LNM PTC without HT组。比较四组患者的发病年龄、性别、肿瘤大小、临床病理特点等临床资料,前期采用人源趋化因子芯片QAH-CHE-1进行基因筛选,利用免疫组化的方法检测四组患者甲状腺乳头状癌组织中趋化因子CCL21、CCL19、CCL8、CXCL5的表达。 结果 :HT较易发生于女性,PTC with HT患者的甲状腺腺外侵犯发生率高于不合并HT的患者,肿瘤直径相对更大。当淋巴结转移时,肿瘤多灶性以及甲状腺腺外侵犯的发生率更高,危险度分层也有中高危的风险。免疫组化结果显示CCL21、CCL19、CCL8、CXCL5在HT合并PTC组织中的阳性表达率高于不合并HT的PTC组织,当有淋巴结转移时,HT合并PTC组织阳性表达率更高,差异具有显著性(P<0.05)。 结论 :趋化因子CCL21、CCL19、CCL8、CXCL5可能与桥本甲状腺炎的慢性刺激在PTC的发生发展中所承担的角色及潜在分子机制相关。
英文摘要:
      Objective:To investigate the clinical significance of relevant chemokines in the tumor microenvironment of papillary thyroid carcinoma (PTC) combined with Hashimoto"s thyroiditis (HT). Methods:The pathological sections of 60 patients with papillary thyroid cancer from May to October 2023 in Zhejiang Provincial People"s Hospital , and were divided into PTC with HT group, PTC without HT group, Lymph Node Metastases (LNM) PTC with HT group and LNM PTC without HT group. Clinical data such as age of onset, gender, tumour size and clinicopathological characteristics of the four groups were compared. Protein chip identification was conducted in the early stage using the human chemokine microarray QAH-CHE-1. The expression of chemokines CCL21, CCL19, CCL8 and CXCL5 in the papillary thyroid cancer tissues of patients was detected by immunohistochemistry methods. Results:It is more likely for HT to occur in women, and patients with PTC and HT have a higher incidence of extra-adenoidal invasion of the thyroid gland than patients without HT, with relatively larger tumour diameters. When lymph node metastasis was present, the incidence of multifocal tumour as well as extra-thyroidal gland invasion was higher, and the risk stratification also had an intermediate to high risk. The immunohistochemical results demonstrated that the positive expression rate of CCL21, CCL19, CCL8, and CXCL5 was higher in PTC tissues combined with HT than in PTC tissues not combined with HT. Furthermore, when there were lymph node metastases, the positive expression rate of PTC tissues combined with HT was even higher, with a statistically significant difference (P < 0.05). Conclusion:Chemokines CCL21, CCL19, CCL8 and CXCL5 may be related to the role in the development of PTC against the backdrop of Hashimoto thyroiditis and the potential molecular mechanism.
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