Division of Otolaryngology, Department of Surgery, Faculty of Medicine, Université de Sherbrooke, CIUSSS de l'Estrie - CHUS, Hôpital Hôtel-Dieu de Sherbrooke, 580 Bowen S, Sherbrooke, QC, J1G 2E8, Canada.
Department of Pathology, Faculty of Medicine, Université de Sherbrooke, CIUSSS de l'Estrie - CHUS, Hôpital Hôtel-Dieu de Sherbrooke, 580 Bowen S, Sherbrooke, QC, J1G 2E8, Canada.
J Otolaryngol Head Neck Surg. 2018 Oct 19;47(1):63. doi: 10.1186/s40463-018-0311-x.
To date, no single molecular marker has been demonstrated as clinically useful in differentiating malignant from benign thyroid nodules when a fine needle aspiration falls in the "unknown significance" categories of the Bethesda Classification. PACE4, a member of the proprotein convertase family of enzymes, has been shown to play a major role in the pathogenesis of prostate cancer, through the formation of an oncogenic isoform named PACE4-altCT. PACE4 isoforms have also been suggested to play a role in other cancers, including thyroid cancer, but have never been investigated in a detailed manner. Our objective is to compare the histochemical distribution of the two major PACE4 isoforms in benign and malignant thyroid nodules, in order to determine their potential usefulness as discriminatory biomarkers.
Thyroid tissues of patients who underwent thyroidectomy were classified according to final pathology. Corresponding tissue sections were immunostained, using two previously validated antibodies raised against the C-terminal end of the two PACE4 isoforms, namely the full-length PACE4 protein (PACE4-FL) and its alternative isoform (PACE4-altCT). Nodules were compared with adjacent normal parenchyma and immunostaining was rated as "low" or "high" by a head and neck pathologist.
Non-lesional thyroid parenchyma did not express PACE4-FL (p = 0.002). As a group, malignant (n = 17) nodules expressed PACE4-FL significantly more than benign (n = 24) nodules (percentage of high immunostaining: 52.9% vs 4.2%; p = 0.001). Reciprocally, there was a statistically lower expression of PACE4-altCT in malignant nodules than in adjacent non-lesional parenchyma (p = 0.014). The specificity of a high PACE4-FL immunostaining in determining malignancy was 95.8% (95% CI, 78.9% to 99.9%).
This study supports the previously described relationship between PACE4-FL and PACE4-altCT through alternative splicing. It also suggests that PACE4-FL is a promising biomarker for thyroid malignancy. Its high specific expression for malignancy could make it an interesting "rule in" test for thyroid cancer. Further prospective, quantitative studies are currently being designed to address how measurements of PACE4 isoforms could be used in a clinical setting.
This study does not report the results of a health care intervention on human participants. It was nonetheless registered on ClinicalTrials.gov under reference number NCT03160482 .
迄今为止,当细针抽吸活检结果落入贝塞斯达分类的“意义不明”类别时,尚无单一分子标志物被证明在区分良恶性甲状腺结节方面具有临床意义。PACE4 是蛋白原转化酶家族的成员之一,已被证明在前列腺癌的发病机制中发挥主要作用,通过形成一种名为 PACE4-altCT 的致癌同工型。PACE4 同工型也被认为在其他癌症中发挥作用,包括甲状腺癌,但从未进行过详细研究。我们的目的是比较良性和恶性甲状腺结节中两种主要 PACE4 同工型的组织化学分布,以确定它们作为鉴别生物标志物的潜在用途。
根据最终病理将接受甲状腺切除术的患者的甲状腺组织进行分类。使用针对两种 PACE4 同工型 C 末端的两种先前验证的抗体对相应的组织切片进行免疫染色,即全长 PACE4 蛋白(PACE4-FL)及其替代同工型(PACE4-altCT)。将结节与相邻正常实质进行比较,由头颈部病理学家对免疫染色进行“低”或“高”评分。
非病变性甲状腺实质不表达 PACE4-FL(p=0.002)。作为一个组,恶性(n=17)结节的 PACE4-FL 表达明显高于良性(n=24)结节(高免疫染色百分比:52.9% vs 4.2%;p=0.001)。相反,恶性结节中 PACE4-altCT 的表达明显低于相邻非病变实质(p=0.014)。高 PACE4-FL 免疫染色确定恶性的特异性为 95.8%(95%CI,78.9%至 99.9%)。
这项研究支持了之前描述的 PACE4-FL 和 PACE4-altCT 通过选择性剪接之间的关系。它还表明 PACE4-FL 是甲状腺恶性肿瘤有前途的生物标志物。其对恶性肿瘤的高特异性表达可能使其成为甲状腺癌的有趣“规则内”检测。目前正在设计进一步的前瞻性、定量研究,以解决如何在临床环境中使用 PACE4 同工型的测量值。
本研究并未报告对人类参与者进行的医疗干预措施的结果。然而,它在 ClinicalTrials.gov 上以注册号 NCT03160482 进行了注册。