Interaction of BANCR in the relationship between Hashimoto’s thyroiditis and papillary thyroid carcinoma expression patterns and possible molecular mechanisms

IF 3.2 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jiabo Zhang, Lingli Yao, Yu Guo
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引用次数: 0

Abstract

Background

Previous studies have established a connection between Hashimoto’s thyroiditis (HT) and an increased risk of papillary thyroid carcinoma (PTC). However, the molecular mechanisms driving this association are not well understood. The long non-coding RNA (lncRNA) BRAF-activated non-coding RNA (BANCR) has been implicated in various cancers, suggesting a potential role in the HT-PTC linkage.

Methods

This study investigated the expression levels of BANCR in PTC and HT samples, compared to control tissues. We also examined the association between BANCR expression and clinicopathological features, including lymph node metastasis. Furthermore, we explored the molecular mechanisms of BANCR in PTC pathogenesis and its potential as a therapeutic target.

Results

BANCR expression was significantly lower in PTC samples than in controls, while it was moderately increased in HT samples. In PTC cases with concurrent HT, BANCR expression was markedly reduced compared to normal tissues. Our analysis revealed BANCR’s role as an oncogene in PTC, influencing various cancer-related signaling pathways. Interestingly, no significant correlation was found between BANCR expression and lymph node metastasis.

Conclusion

Our findings underscore the involvement of BANCR in the connection between HT and PTC. The distinct expression patterns of BANCR in PTC and HT, especially in PTC with concurrent HT, provide new insights into the molecular interplay between these conditions. This study opens avenues for the development of innovative diagnostic and therapeutic strategies targeting BANCR in PTC and HT.

Abstract Image

BANCR在桥本氏甲状腺炎与甲状腺乳头状癌表达模式之间的相互作用及可能的分子机制。
背景:以往的研究已证实桥本氏甲状腺炎(HT)与甲状腺乳头状癌(PTC)风险增加之间存在联系。然而,导致这种关联的分子机制尚不十分清楚。长非编码 RNA(lncRNA)BRAF 激活的非编码 RNA(BANCR)与多种癌症有关联,这表明它在 HT-PTC 关联中可能发挥作用:本研究调查了与对照组织相比,BANCR 在 PTC 和 HT 样本中的表达水平。我们还研究了 BANCR 表达与临床病理特征(包括淋巴结转移)之间的关联。此外,我们还探讨了BANCR在PTC发病机制中的分子机制及其作为治疗靶点的潜力:结果:BANCR 在 PTC 样本中的表达明显低于对照组,而在 HT 样本中则适度升高。在并发 HT 的 PTC 病例中,与正常组织相比,BANCR 的表达明显降低。我们的分析表明,BANCR 在 PTC 中扮演着癌基因的角色,影响着各种与癌症相关的信号通路。有趣的是,BANCR的表达与淋巴结转移之间没有发现明显的相关性:我们的研究结果表明,BANCR 参与了 HT 与 PTC 之间的联系。BANCR在PTC和HT中的不同表达模式,尤其是在同时伴有HT的PTC中的不同表达模式,为这些疾病之间的分子相互作用提供了新的见解。这项研究为开发针对 PTC 和 HT 中 BANCR 的创新诊断和治疗策略开辟了道路。
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来源期刊
Journal of Gene Medicine
Journal of Gene Medicine 医学-生物工程与应用微生物
CiteScore
6.40
自引率
0.00%
发文量
80
审稿时长
6-12 weeks
期刊介绍: The aims and scope of The Journal of Gene Medicine include cutting-edge science of gene transfer and its applications in gene and cell therapy, genome editing with precision nucleases, epigenetic modifications of host genome by small molecules, siRNA, microRNA and other noncoding RNAs as therapeutic gene-modulating agents or targets, biomarkers for precision medicine, and gene-based prognostic/diagnostic studies. Key areas of interest are the design of novel synthetic and viral vectors, novel therapeutic nucleic acids such as mRNA, modified microRNAs and siRNAs, antagomirs, aptamers, antisense and exon-skipping agents, refined genome editing tools using nucleic acid /protein combinations, physically or biologically targeted delivery and gene modulation, ex vivo or in vivo pharmacological studies including animal models, and human clinical trials. Papers presenting research into the mechanisms underlying transfer and action of gene medicines, the application of the new technologies for stem cell modification or nucleic acid based vaccines, the identification of new genetic or epigenetic variations as biomarkers to direct precision medicine, and the preclinical/clinical development of gene/expression signatures indicative of diagnosis or predictive of prognosis are also encouraged.
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