UMM Logo

Universitas Muhammadiyah Malang

Free Download Journals Directory

International Journal Of Bilogical Sciences

.: Home > International Journal Of Bilogical Sciences > 2014 > Volume 10 Number 7 > Yanchao Huang1,2, Nathan Benaich1,4, Christopher Tape1,5, Hang Fai Kwok1,3* and Gillian Murphy1*

Targeting the Sheddase Activity of ADAM17 by an Anti-ADAM17 Antibody D1(A12) Inhibits Head and Neck Squamous Cell Carcinoma Cell Proliferation and Motility via Blockage of Bradykinin Induced HERs Transactivation

Yanchao Huang1,2, Nathan Benaich1,4, Christopher Tape1,5, Hang Fai Kwok1,3* and Gillian Murphy1*
1. Cancer Research UK Cambridge Institute, University of Cambridge, Department of Oncology, UK 2. IONTAS Ltd, Hopkins Building, Tennis Court Rd., Cambridge CB2 1QW, UK (current address) 3. Faculty of Health Sciences, University of Macau, Macau (current address) 4. Centre for Stem Cells and Regenerative Medicine, King's College London School of Medicine, 28th Floor, Tower Wing, Guy’s Hospital, Great Maze Pond, London SE1 9RT, UK (current address) 5. The Institute of Cancer Research, 237 Fulham Road, London, SW3 6JB, UK (current address). * Joint senior authors.  Corresponding authors: (Y.H) / (H.F.K).
Abstract :

A disintegrin and metalloproteinase 17 (ADAM17) regulates key cellular processes including proliferation and migration through the shedding of a diverse array of substrates such as epidermal growth factor receptor (EGFR) ligands. ADAM17 is implicated in the pathogenesis of many diseases including rheumatoid arthritis and cancers such as head and neck squamous cell carcinoma (HNSCC). As a central mediator of cellular events, overexpressed EGFR is a validated molecular target in HNSCC. However, EGFR inhibition constantly leads to tumour resistance. One possible mechanism of resistance is the activation of alternative EGFR family receptors and downstream pathways via the release of their ligands. Here, we report that treating human HNSCC cells in vitro with a human anti-ADAM17 inhibitory antibody, D1(A12), suppresses proliferation and motility in the absence or presence of the EGFR tyrosine kinase inhibitor (TKI) gefitinib. Treatment with D1(A12) decreases both the endogenous and the bradykinin (BK)-stimulated shedding of HER ligands, accompanied by a reduction in the phosphorylation of HER receptors and downstream signalling pathways including STAT3, AKT and ERK. Knockdown of ADAM17, but not ADAM10, also suppresses HNSCC cell proliferation and migration. Furthermore, we show that heregulin (HRG) and heparin-binding epidermal growth factor like growth factor (HB-EGF) predominantly participate in proliferation and migration, respectively. Taken together, these results demonstrate that D1(A12)-mediated inhibition of cell proliferation, motility, phosphorylation of HER receptors and downstream signalling is achieved via reduced shedding of ADAM17 ligands. These findings underscore the importance of ADAM17 and suggest that D1(A12) might be an effective targeted agent for treating EGFR TKI-resistant HNSCC.

Keywords :
ADAM17, inhibitory antibody, HER receptor and ligands, cell proliferation and motility.

Date Deposited : 12 Feb 2016 10:08

Last Modified : 12 Feb 2016 10:08

Official URL:

Volume 10, Number 7, - 2014 , ISSN 1449-2288

Full Text Original
Abstract : pdf doc