Literature DB >> 31932491

Cannabinoids Promote Progression of HPV-Positive Head and Neck Squamous Cell Carcinoma via p38 MAPK Activation.

Chao Liu1,2, Sayed H Sadat1, Koji Ebisumoto1, Akihiro Sakai1, Bharat A Panuganti3, Shuling Ren1,2, Yusuke Goto1, Sunny Haft1, Takahito Fukusumi1, Mizuo Ando1, Yuki Saito1, Theresa Guo4, Pablo Tamayo1, Huwate Yeerna1, William Kim1, Jacqueline Hubbard5, Andrew B Sharabi6, J Silvio Gutkind1, Joseph A Califano7,3.   

Abstract

PURPOSE: Human papillomavirus (HPV)-related head and neck squamous cell carcinoma (HNSCC) is associated with daily marijuana use and is also increasing in parallel with increased marijuana use in the United States. Our study is designed to define the interaction between cannabinoids and HPV-positive HNSCC. EXPERIMENTAL
DESIGN: The expression of cannabinoid receptors CNR1 and CNR2 was analyzed using The Cancer Genome Atlas (TCGA) HNSCC data. We used agonists, antagonists, siRNAs, or shRNA-based models to explore the roles of CNR1 and CNR2 in HPV-positive HNSCC cell lines and animal models. Cannabinoid downstream pathways involved were determined by Western blotting and analyzed in a primary HPV HNSCC cohort with single-sample gene set enrichment analysis (ssGSEA) and the OncoGenome Positioning System (Onco-GPS).
RESULTS: In TCGA cohort, the expression of CNR1 and CNR2 was elevated in HPV-positive HNSCC compared with HPV-negative HNSCC, and knockdown of CNR1/CNR2 expression inhibited proliferation in HPV-positive HNSCC cell lines. Specific CNR1 and CNR2 activation as well as nonselective cannabinoid receptor activation in cell lines and animal models promoted cell growth, migration, and inhibited apoptosis through p38 MAPK pathway activation. CNR1/CNR2 antagonists suppressed cell proliferation and migration and induced apoptosis. Using whole-genome expression analysis in a primary HPV HNSCC cohort, we identified specific p38 MAPK pathway activation signature in tumors from HPV HNSCC patients with objective measurement of concurrent cannabinoid exposure.
CONCLUSIONS: Cannabinoids can promote progression of HPV-positive HNSCC through p38 MAPK pathway activation. ©2020 American Association for Cancer Research.

Entities:  

Year:  2020        PMID: 31932491      PMCID: PMC7538010          DOI: 10.1158/1078-0432.CCR-18-3301

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  53 in total

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Journal:  Clin Chem       Date:  2011-08-11       Impact factor: 8.327

Review 2.  G protein regulation of MAPK networks.

Authors:  Z G Goldsmith; D N Dhanasekaran
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3.  Use of cannabinoids in cancer care: palliative care.

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4.  A role for p38 MAPK in head and neck cancer cell growth and tumor-induced angiogenesis and lymphangiogenesis.

Authors:  Kantima Leelahavanichkul; Panomwat Amornphimoltham; Alfredo A Molinolo; John R Basile; Sittichai Koontongkaew; J Silvio Gutkind
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Review 5.  The PI3K/Akt/mTOR axis in head and neck cancer: functions, aberrations, cross-talk, and therapies.

Authors:  R Vander Broek; S Mohan; D F Eytan; Z Chen; C Van Waes
Journal:  Oral Dis       Date:  2013-12-23       Impact factor: 3.511

6.  Cannabinoid receptor-2 immunoreactivity is associated with survival in squamous cell carcinoma of the head and neck.

Authors:  Thomas J W Klein Nulent; Paul J Van Diest; Petra van der Groep; Frank K J Leusink; Cas L J J Kruitwagen; Ronald Koole; Ellen M Van Cann
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7.  Evaluation of cannabinoid CB1 and CB2 receptors expression in mobile tongue squamous cell carcinoma: associations with clinicopathological parameters and patients' survival.

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8.  Cannabinoids induce cancer cell proliferation via tumor necrosis factor alpha-converting enzyme (TACE/ADAM17)-mediated transactivation of the epidermal growth factor receptor.

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Review 2.  Unintended Effects of GPCR-Targeted Drugs on the Cancer Phenotype.

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