Angiopoietin-like 4 is upregulated by amphiregulin and activates cell proliferation and migration through p38 kinase in head and neck squamous cell carcinoma

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Ajay Kumar, Emmanuel Asiedu, Eman Hefni, Cheryl Armstrong, Deepak Menon, Tao Ma, Lauren Sands, Eberechi Mbadugha, Akrit Sodhi, Abraham Schneider, Silvia Montaner
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Abstract

Background

Angiopoietin-like 4 is a molecular hallmark that correlates with the growth and metastasis of head and neck squamous cell carcinoma, one of the most prevalent cancers worldwide. However, the molecular mechanisms by which angiopoietin-like 4 promotes head and neck squamous cell carcinoma tumorigenesis are unclear.

Methods

Using well-characterized cell lines of head and neck squamous cell carcinoma development, including human normal oral keratinocytes, dysplastic oral keratinocytes, oral leukoplakia-derived oral keratinocytes, and head and neck squamous cell carcinoma cell lines, HN13, HN6, HN4, HN12, and CAL27, we investigated the signaling pathways upstream and downstream of angiopoietin-like 4-induced head and neck squamous cell carcinoma tumorigenesis.

Results

We found that both epidermal growth factor receptor ligands, epithelial growth factor, and amphiregulin led to angiopoietin-like 4 upregulation in normal oral keratinocytes and dysplastic oral keratinocytes and cooperated with the activation of hypoxia-inducible factor-1 in this effect. Interestingly, amphiregulin and angiopoietin-like 4 were increased in dysplastic oral keratinocytes and head and neck squamous cell carcinoma cell lines, and amphiregulin-induced activation of cell proliferation was dependent on angiopoietin-like 4. Although both p38 mitogen-activated protein kinases (p38 MAPK) and protein kinase B (AKT) were activated by angiopoietin-like 4, only pharmacological inhibition of p38 MAPK was sufficient to prevent head and neck squamous cell carcinoma cell proliferation and migration. We further observed that angiopoietin-like 4 promoted the secretion of interleukin 11 (IL-11), interleukin 12 (IL-12), interleukin-1 alpha (IL-1α), vascular endothelial growth factor, platelet-derived growth factor (PDGF), and tumour necrosis factor alpha (TNF-α), cytokines and chemokines previously implicated in head and neck squamous cell carcinoma pathogenesis.

Conclusion

Our results demonstrate that angiopoietin-like 4 is a downstream effector of amphiregulin and promotes head and neck squamous cell carcinoma development both through direct activation of p38 kinase as well as paracrine mechanisms.

在头颈部鳞状细胞癌中,血管生成素样 4 受安非拉酮上调,并通过 p38 激酶激活细胞增殖和迁移。
背景:血管生成素样 4 是头颈部鳞状细胞癌(全球最常见的癌症之一)生长和转移的分子标志。然而,血管生成素样 4 促进头颈部鳞状细胞癌肿瘤发生的分子机制尚不清楚:方法:我们利用表征良好的头颈部鳞状细胞癌细胞系,包括人类正常口腔角朊细胞、发育不良的口腔角朊细胞、口腔白斑衍生的口腔角朊细胞以及头颈部鳞状细胞癌细胞系 HN13、HN6、HN4、HN12 和 CAL27,研究了血管生成素样 4 诱导头颈部鳞状细胞癌肿瘤发生的上下游信号通路:结果:我们发现表皮生长因子受体配体、上皮生长因子和两性胰岛素都会导致血管生成素样 4 在正常口腔角朊细胞和发育不良的口腔角朊细胞中上调,并与缺氧诱导因子-1 的激活共同发挥作用。有趣的是,两性胰岛素和血管生成素样 4 在发育不良的口腔角朊细胞和头颈部鳞状细胞癌细胞系中均有增加,两性胰岛素诱导的细胞增殖激活依赖于血管生成素样 4。虽然 p38 丝裂原活化蛋白激酶(p38 MAPK)和蛋白激酶 B(AKT)都被类血管生成素 4 激活,但只有药物抑制 p38 MAPK 才能阻止头颈部鳞状细胞癌细胞的增殖和迁移。我们进一步观察到,类血管生成素 4 促进了白细胞介素 11(IL-11)、白细胞介素 12(IL-12)、白细胞介素-1 α(IL-1α)、血管内皮生长因子、血小板衍生生长因子(PDGF)和肿瘤坏死因子α(TNF-α)的分泌,这些细胞因子和趋化因子以前曾与头颈部鳞状细胞癌的发病机制有关:我们的研究结果表明,血管生成素样 4 是两性胰岛素的下游效应因子,通过直接激活 p38 激酶和旁分泌机制促进头颈部鳞状细胞癌的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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