4.8 Article

MUC4 regulates cellular senescence in head and neck squamous cell carcinoma through p16/Rb pathway

Journal

ONCOGENE
Volume 34, Issue 13, Pages 1698-1708

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2014.102

Keywords

-

Funding

  1. National Institutes of Health [RO1 CA133774, U54 CA163120, UO1 CA111294, P50 CA 127297, R21 CA156037, P20 RR021937]
  2. NATIONAL CANCER INSTITUTE [U01CA111294, P50CA127297, R21CA156037, U54CA163120, R01CA133774] Funding Source: NIH RePORTER
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [P20RR021937] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [P20GM103480] Funding Source: NIH RePORTER

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The limited effectiveness of therapy for patients with advanced stage head and neck squamous cell carcinoma (HNSCC) or recurrent disease is a reflection of an incomplete understanding of the molecular basis of HNSCC pathogenesis. MUC4, a high molecular weight glycoprotein, is differentially overexpressed in many human cancers and implicated in cancer progression and resistance to several chemotherapies. However, its clinical relevance and the molecular mechanisms through which it mediates HNSCC progression are not well understood. This study revealed a significant upregulation of MUC4 in 78% (68/87) of HNSCC tissues compared with 10% positivity (1/10) in benign samples (P = 0.006, odds ratio (95% confidence interval) = 10.74 (2.0-57.56). MUC4 knockdown (KD) in SCC1 and SCC10B HNSCC cell lines resulted in significant inhibition of growth in vitro and in vivo, increased senescence as indicated by an increase in the number of flat, enlarged and senescence-associated beta-galactosidase (SA-beta-Gal)positive cells. Decreased cellular proliferation was associated with G(0)/G(1) cell cycle arrest and decrease expression of cell cycle regulatory proteins like cyclin E, cyclin D1 and decrease in BrdU incorporation. Mechanistic studies revealed upregulation of p16, pRb dephosphorylation and its interaction with histone deacetylase 1/2. This resulted in decreased histone acetylation (H3K9) at cyclin E promoter leading to its downregulation. Orthotopic implantation of MUC4 KD SCC1 cells into the floor of the mouth in nude mice resulted in the formation of significantly smaller tumors (170 +/- 18.30 mg) compared to those (375 +/- 17.29 mg) formed by control cells (P = 0.00007). In conclusion, our findings showed that MUC4 overexpression has a critical role by regulating proliferation and cellular senescence of HNSCC cells. Downregulation of MUC4 may be a promising therapeutic approach for treating HNSCC patients.

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