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甲状旁腺激素样激素是头颈部癌症的不良预后标志物,并通过 RUNX2 调控促进细胞生长。

Parathyroid Hormone-Like Hormone is a Poor Prognosis Marker of Head and Neck Cancer and Promotes Cell Growth via RUNX2 Regulation.

机构信息

Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.

National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.

出版信息

Sci Rep. 2017 Jan 25;7:41131. doi: 10.1038/srep41131.

DOI:10.1038/srep41131
PMID:28120940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5264159/
Abstract

Parathyroid Hormone-Like Hormone (PTHLH) is an autocrine/paracrine ligand that is up-regulated in head and neck squamous cell carcinoma (HNSCC). However, the cellular function and regulatory mechanism in HNSCC remains obscure. We investigated the clinical significance of PTHLH in HNSCC patients, and verified the role of RUNX2/PTHLH axis, which is stimulated HNSCC cell growth. In patients, PTHLH is a poor prognosis marker. PTHLH expression lead to increasing the cell proliferation potential through an autocrine/paracrine role and elevating blood calcium level in Nod-SCID mice. In public HNSCC microarray cohorts, PTHLH is found to be co-expressed with RUNX2. Physiologically, PTHLH is regulated by RUNX2 and also acting as key calcium regulator. However, elevations of calcium concentration also increased the RUNX2 expression. PTHLH, calcium, and RUNX2 form a positive feedback loop in HNSCC. Furthermore, ectopic RUNX2 expression also increased PTHLH expression and promoted proliferation potential through PTHLH expression. Using cDNA microarray analysis, we found PTHLH also stimulated expression of cell cycle regulators, namely CCNA2, CCNE2, and CDC25A in HNSCC cells, and these genes are also up-regulated in HNSCC patients. In summary, our results reveal that PTHLH expression is a poor prognosis marker in HNSCC patients, and RUNX2-PTHLH axis contributes to HNSCC tumor growth.

摘要

甲状旁腺激素样激素(PTHLH)是一种自分泌/旁分泌配体,在头颈部鳞状细胞癌(HNSCC)中上调。然而,HNSCC 中的细胞功能和调节机制仍然不清楚。我们研究了 PTHLH 在 HNSCC 患者中的临床意义,并验证了 RUNX2/PTHLH 轴的作用,该轴刺激 HNSCC 细胞生长。在患者中,PTHLH 是预后不良的标志物。PTHLH 表达通过自分泌/旁分泌作用导致细胞增殖潜力增加,并在 Nod-SCID 小鼠中升高血钙水平。在公共 HNSCC 微阵列队列中,发现 PTHLH 与 RUNX2 共表达。在生理上,PTHLH 受 RUNX2 调节,也是关键的钙调节剂。然而,钙浓度的升高也增加了 RUNX2 的表达。PTHLH、钙和 RUNX2 在 HNSCC 中形成正反馈回路。此外,异位 RUNX2 表达也通过 PTHLH 表达增加 PTHLH 表达并促进增殖潜力。通过 cDNA 微阵列分析,我们发现 PTHLH 还刺激 HNSCC 细胞中细胞周期调节剂的表达,即 CCNA2、CCNE2 和 CDC25A,并且这些基因在 HNSCC 患者中也上调。总之,我们的结果表明,PTHLH 表达是 HNSCC 患者预后不良的标志物,RUNX2-PTHLH 轴促进 HNSCC 肿瘤生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/859dd856801d/srep41131-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/1bd480833ff1/srep41131-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/8a739b50561b/srep41131-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/d20812bd68e3/srep41131-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/cfe023af59c7/srep41131-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/98ce99c624ce/srep41131-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/859dd856801d/srep41131-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/1bd480833ff1/srep41131-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/8a739b50561b/srep41131-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/d20812bd68e3/srep41131-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/cfe023af59c7/srep41131-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/98ce99c624ce/srep41131-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4285/5264159/859dd856801d/srep41131-f6.jpg

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