Research Center, St. Pietro Fatebenefratelli Hospital, Rome, Italy.
PLoS One. 2011;6(6):e20665. doi: 10.1371/journal.pone.0020665. Epub 2011 Jun 17.
Galectin-3 (Gal-3) is an anti-apoptotic molecule involved in thyroid cells transformation. It is specifically overexpressed in thyroid tumour cells and is currently used as a preoperative diagnostic marker of thyroid malignancy. Gal-3 expression is downregulated by wt-p53 at the transcriptional level. In well-differentiated thyroid carcinomas (WDTCs) there is an unexplained paradoxical concomitant expression of Gal-3 and wt-p53. HIPK2 is a co-regulator of different transcription factors, and modulates basic cellular processes mainly through the activation of wt-p53. Since we demonstrated that HIPK2 is involved in p53-mediated Gal-3 downregulation, we asked whether HIPK2 deficiency might be responsible for such paradoxical Gal-3 overexpression in WDTC.
METHODOLOGY/PRINCIPAL FINDINGS: We analyzed HIPK2 protein and mRNA levels, as well as loss of heterozygosity (LOH) at the HIPK2 locus (7q32-34), in thyroid tissue samples. HIPK2 protein levels were high in all follicular hyperplasias (FHs) analyzed. Conversely, HIPK2 was undetectable in 91.7% of papillary thyroid carcinomas (PTCs) and in 60.0% of follicular thyroid carcinomas (FTCs). HIPK2 mRNA levels were upregulated in FH compared to normal thyroid tissue (NTT), while PTC showed mean HIPK2 mRNA levels lower than FH and, in 61.5% of cases, also lower than NTT. We found LOH at HIPK-2 gene locus in 37.5% of PTCs, 14.3% of FTCs and 18.2% of follicular adenomas. To causally link these data with Gal-3 upregulation, we performed in vitro experiments, using the PTC-derived K1 cells, in which HIPK2 expression was manipulated by RNA interference (RNAi) or plasmid-mediated overexpression. HIPK2 RNAi was associated with Gal-3 upregulation, while HIPK2 overexpression with Gal-3 downregulation.
CONCLUSIONS/SIGNIFICANCE: Our results indicate that HIPK2 expression and function are impaired in WDTCs, in particular in PTCs, and that this event explains Gal-3 overexpression typically observed in these types of tumours. Therefore, HIPK2 can be considered as a new tumour suppressor gene for thyroid cancers.
半乳糖凝集素-3(Gal-3)是一种参与甲状腺细胞转化的抗细胞凋亡分子。它在甲状腺肿瘤细胞中特异性过表达,目前被用作甲状腺恶性肿瘤的术前诊断标志物。Gal-3 的表达在转录水平上受到 wt-p53 的下调。在分化良好的甲状腺癌(WDTC)中,存在 Gal-3 和 wt-p53 同时表达的无法解释的矛盾现象。HIPK2 是不同转录因子的共调节剂,主要通过激活 wt-p53 来调节基本的细胞过程。由于我们已经证明 HIPK2 参与 p53 介导的 Gal-3 下调,我们想知道 HIPK2 缺陷是否是 WDTC 中这种矛盾的 Gal-3 过表达的原因。
方法/主要发现:我们分析了甲状腺组织样本中的 HIPK2 蛋白和 mRNA 水平以及 HIPK2 基因座(7q32-34)的杂合性丢失(LOH)。在所有分析的滤泡性增生(FH)中,HIPK2 蛋白水平均较高。相反,91.7%的甲状腺乳头状癌(PTC)和 60.0%的滤泡状甲状腺癌(FTC)中无法检测到 HIPK2。与正常甲状腺组织(NTT)相比,FH 中 HIPK2 mRNA 水平上调,而 PTC 中 HIPK2 mRNA 水平低于 FH,在 61.5%的情况下也低于 NTT。我们在 37.5%的 PTC、14.3%的 FTC 和 18.2%的滤泡性腺瘤中发现 HIPK-2 基因座的 LOH。为了将这些数据与 Gal-3 上调相关联,我们使用 PTC 衍生的 K1 细胞进行了体外实验,在这些细胞中,通过 RNA 干扰(RNAi)或质粒介导的过表达来操纵 HIPK2 表达。HIPK2 RNAi 与 Gal-3 上调相关,而 HIPK2 过表达与 Gal-3 下调相关。
结论/意义:我们的结果表明,HIPK2 在 WDTC 中,特别是在 PTC 中表达和功能受损,这一事件解释了通常在这些类型的肿瘤中观察到的 Gal-3 过表达。因此,HIPK2 可以被认为是甲状腺癌的一种新的肿瘤抑制基因。