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

Author:

Kumar Ajay1ORCID,Asiedu Emmanuel1,Hefni Eman12,Armstrong Cheryl1,Menon Deepak1,Ma Tao1,Sands Lauren1,Mbadugha Eberechi1,Sodhi Akrit3,Schneider Abraham14ORCID,Montaner Silvia14

Affiliation:

1. Department of Oncology and Diagnostic Sciences, School of Dentistry University of Maryland Baltimore Maryland USA

2. Department of Basic and Clinical Oral Sciences, College of Dental Medicine Umm Al Qura University Makkah Saudi Arabia

3. Wilmer Eye Institute Johns Hopkins University School of Medicine Baltimore Maryland USA

4. Greenebaum Comprehensive Cancer Center University of Maryland Baltimore Maryland USA

Abstract

AbstractBackgroundAngiopoietin‐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.MethodsUsing 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.ResultsWe 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.ConclusionOur 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.

Funder

Umm Al-Qura University

Saudi Arabian Cultural Mission

Publisher

Wiley

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