Wang Yinghao, Jin Yixiang, Bhandari Adheesh, Yao Zhihan, Yang Fan, Pan Yiyuan, Zheng Zhouci, Lv Shixu, Wang Ouchen
Department of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, People's Republic of China.
Onco Targets Ther. 2017 Dec 21;11:37-46. doi: 10.2147/OTT.S149613. eCollection 2018.
Thyroid cancer is the most commonly reported endocrine malignancy, and its increased incidence has been the highest in all human tumors in recent decades. To investigate the mechanism of papillary thyroid cancer (PTC) occurrence and progression, we performed RNA sequencing and found an upregulated gene, . However, the biological function of is still not clear.
We analyzed expression using The Cancer Genome Atlas (TCGA) database and hypothesized to be a gene associated with PTC. To test this hypothesis, we collected 89 pairs of thyroid nodules and adjacent normal thyroid tissues (56 pairs of PTCs, 33 pairs of benign thyroid nodules). Afterward, we performed real-time quantitative polymerase chain reaction (RT-qPCR) to investigate expression in thyroid nodule patients, and then analyzed clinicopathologic features. We performed proliferation, colony formation, migration, and invasion assays to determine the function of in PTC.
We demonstrated that plays oncogenic roles in PTC. The relative expression of is significantly upregulated in PTC compared with matched thyroid normal tissues in validated cohort and TCGA cohort (<0.001). We also checked area under the curve (AUC of receiver operator characteristic [ROC]) of 97.3% for validated cohort and 90.1% for TCGA cohort to differentiate PTC tumors from normal tissues. In clinicopathologic feature analysis, we found that upregulated is closely related to lymph node metastasis (=0.018). Furthermore, knockdown of inhibited the proliferation, colony formation, migration, and invasive capacity of PTC.
This study indicated that is a gene associated with PTC.
甲状腺癌是最常报道的内分泌恶性肿瘤,近几十年来其发病率的增长在所有人类肿瘤中位居榜首。为了探究甲状腺乳头状癌(PTC)发生和进展的机制,我们进行了RNA测序,发现了一个上调基因, 。然而, 的生物学功能仍不清楚。
我们使用癌症基因组图谱(TCGA)数据库分析 的表达,并假设 是与PTC相关的基因。为了验证这一假设,我们收集了89对甲状腺结节及相邻正常甲状腺组织(56对PTC,33对良性甲状腺结节)。随后,我们进行实时定量聚合酶链反应(RT-qPCR)以研究甲状腺结节患者中 的表达,然后分析临床病理特征。我们进行了增殖、集落形成、迁移和侵袭试验,以确定 在PTC中的功能。
我们证明 在PTC中发挥致癌作用。在验证队列和TCGA队列中,与匹配的甲状腺正常组织相比,PTC中 的相对表达显著上调(<0.001)。我们还检查了验证队列的曲线下面积(受试者操作特征曲线[ROC]的AUC)为97.3%,TCGA队列的为90.1%,以区分PTC肿瘤与正常组织。在临床病理特征分析中,我们发现 上调与淋巴结转移密切相关(=0.018)。此外,敲低 可抑制PTC的增殖、集落形成、迁移和侵袭能力。
本研究表明 是与PTC相关的基因。