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FBP1 过表达抑制甲状腺乳头状癌中的 HIF-1α。

FBP1 over-expression suppresses HIF-1α in papillary thyroid cancer.

机构信息

General Surgery Department, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.

Breast Surgery Department, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.

出版信息

Sci Rep. 2024 Nov 25;14(1):29167. doi: 10.1038/s41598-024-81017-6.

Abstract

Papillary thyroid carcinoma (PTC) is generally a slow-growing disease with a favorable 10-year survival rate. However, about 10% of PTC cases show significant aggressiveness, with tendencies for local invasion or distant metastasis, the mechanisms of which remain unclear. This study aims to identify predictive indicators and explore new potential targets for clinical treatment, highlighting the need for novel biomarkers and therapeutic targets. We analyzed FBP1 expression in PTC tissues. Cell proliferation, apoptosis, and invasion were evaluated with and without FBP1 overexpression in PTC cells to assess FBP1's effects. We then investigated whether FBP1 reduces PTC cell tumorigenesis and metastasis by regulating HIF-1α expression. FBP1 expression was reduced in PTC samples and showed a negative correlation with T stage. In vitro experiments indicated that FBP1 acts as a hypoxia response inhibitor, regulating tumor cells. Additionally, FBP1 inhibited the proliferation, apoptosis, and invasion of thyroid cancer cells by modulating HIF-1α expression. Our results provide new insights into the role of FBP1 in PTC progression and indicate that targeting the FBP1-HIF-1α axis could be a promising therapeutic approach for this disease.

摘要

甲状腺乳头状癌(PTC)通常是一种生长缓慢的疾病,其 10 年生存率较高。然而,约 10%的 PTC 病例表现出明显的侵袭性,倾向于局部侵犯或远处转移,其机制尚不清楚。本研究旨在寻找预测指标,并探索新的潜在治疗靶点,强调需要新的生物标志物和治疗靶点。我们分析了 PTC 组织中的 FBP1 表达。通过在 PTC 细胞中过表达 FBP1 或不表达 FBP1 来评估细胞增殖、凋亡和侵袭,以评估 FBP1 的作用。然后,我们研究了 FBP1 是否通过调节 HIF-1α 表达来降低 PTC 细胞的肿瘤发生和转移。FBP1 在 PTC 样本中的表达降低,与 T 分期呈负相关。体外实验表明,FBP1 作为缺氧反应抑制剂调节肿瘤细胞。此外,FBP1 通过调节 HIF-1α 表达抑制甲状腺癌细胞的增殖、凋亡和侵袭。我们的研究结果提供了 FBP1 在 PTC 进展中的作用的新见解,并表明靶向 FBP1-HIF-1α 轴可能是治疗这种疾病的一种有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/416b/11589751/97e5dcc59a47/41598_2024_81017_Fig1_HTML.jpg

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