The long-term objective of this application is to identify the molecular and genetic determinants which promote the invasive growth and metastasis of head and neck squamous cell carcinomas (SCC). The poor prognosis of patients with SCC is due to the high invasive growth potential of these tumors, resulting in early regional lymph node and subsequent distant metastasis. The invasive growth, which is instrumental in invasion and metastasis of SCC, is a complex multistage process in which cell-cell dissociation combines with movement, matrix degradation and survival. During the last funding period, we have demonstrated that hepatocyte growth factor (HGF)/c-Met inhibits anoikis induced by a loss of cell-matrix interaction and promotes SCC progression. In this competing renewal, we hypothesize that HGF/c-Met plays an integral role in the invasive growth by stimulating transcription of invasive genes. We propose to employ molecular and genetic approaches to examine how HGF-induced genes promote the invasive growth of SCC cells and how these genes are epigenetically regulated in SCC cells. There are four specific aims.
In Aim 1, we will examine how Mcl-1 induced by HGF inhibits anoikis which is critical for the invasive SCC cells and whether c-Met inhibitors abolish anoikis resistance induced by HGF.
In Aim 2, we will determine whether the AP-1 family member Fra-1 plays a role in invasive growth of SCC cells induced by HGF and is associated with SCC metastasis.
In Aim 3, we will explore how the transcription co-activators are recruited to the Fra-1 promoter to activate transcription.
In Aim 4, we will explore how histone methylation and chromatin remodeling regulate HGF-stimulating transcription and invasive growth. The novel findings from this application may have important implications in developing therapeutic strategies to interfere with the invasive growth and metastasis of SCC and other human cancers.

Public Health Relevance

Squamous cell carcinoma (SCC) is the most common cancer of the head and neck. Advanced SCC with metastasis is often incurable and possesses poor prognosis. Hepatocyte growth factor (HGF) has been found to play an important role in SCC metastasis by stimulating the invasive growth of SCC cells. The long-term objectives of this application are to understand why head and neck SCC and other malignant cancers frequently leave their original site and spread to local and distant organs. In this application, we will examine how HGF stimulates invasion and survival of SCC cells by inducing new gene expression. We will determine whether HGF target genes are abnormally expressed in human SCC tumors and are associated with metastasis. New findings from this study will help us to develop novel strategies for treating SCC and other human cancers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE015964-09
Application #
8269541
Study Section
Tumor Progression and Metastasis Study Section (TPM)
Program Officer
Venkatachalam, Sundaresan
Project Start
2004-04-01
Project End
2015-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
9
Fiscal Year
2012
Total Cost
$458,170
Indirect Cost
$114,324
Name
University of California Los Angeles
Department
Dentistry
Type
Schools of Dentistry
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Chang, Insoon; Wang, Cun-Yu (2016) Inhibition of HDAC6 Protein Enhances Bortezomib-induced Apoptosis in Head and Neck Squamous Cell Carcinoma (HNSCC) by Reducing Autophagy. J Biol Chem 291:18199-209
Plouffe, Steven W; Meng, Zhipeng; Lin, Kimberly C et al. (2016) Characterization of Hippo Pathway Components by Gene Inactivation. Mol Cell 64:993-1008
Ramadoss, S; Guo, G; Wang, C-Y (2016) Lysine demethylase KDM3A regulates breast cancer cell invasion and apoptosis by targeting histone and the non-histone protein p53. Oncogene :
Yu, Fa-Xing; Zhao, Bin; Guan, Kun-Liang (2015) Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer. Cell 163:811-28
Mo, Jung-Soon; Meng, Zhipeng; Kim, Young Chul et al. (2015) Cellular energy stress induces AMPK-mediated regulation of YAP and the Hippo pathway. Nat Cell Biol 17:500-10
Tang, Eric D; Wang, Cun-Yu (2015) YAP-mediated induction of monoacylglycerol lipase restrains oncogenic transformation. Cell Signal 27:836-40
Park, Hyun Woo; Kim, Young Chul; Yu, Bo et al. (2015) Alternative Wnt Signaling Activates YAP/TAZ. Cell 162:780-94
Li, Jiong; Chen, Xiaohong; Ding, Xiangming et al. (2013) LATS2 suppresses oncogenic Wnt signaling by disrupting β-catenin/BCL9 interaction. Cell Rep 5:1650-63
Ding, Xiangming; Pan, Hongya; Li, Jiong et al. (2013) Epigenetic activation of AP1 promotes squamous cell carcinoma metastasis. Sci Signal 6:ra28.1-13, S0-15
Wu, Longtao; Zhao, Jonathan C; Kim, Jung et al. (2013) ERG is a critical regulator of Wnt/LEF1 signaling in prostate cancer. Cancer Res 73:6068-79

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