Identification of Lethal microRNAs Specific for Head and Neck Cancer

Purpose: The prognosis of head and neck squamous cell carcinomas (HNSCC) remains disappointing and the development of novel anti-cancer agents is urgently awaited. We identified by a functional genetic screen microRNAs that are selectively lethal for head and neck cancer cells but not for normal cells. We further investigated the genes targeted by these microRNAs. Experimental Design: A retroviral expression library of human microRNAs was introduced in HNSCC cell lines and normal oropharyngeal keratinocytes to identify tumor-selective lethal microRNAs. Potential downstream gene targets of these microRNAs were identified by gene expression profiling and validated by functional assays. Results: We identified six microRNAs that selectively inhibit proliferation of head and neck cancer cells. By gene expression profiling and 3′-untranslated region (UTR) luciferase reporter assays, we showed that the ataxia telangiectasia mutated (ATM) gene is a common target for at least two and likely three of these microRNAs. Specific inhibition of ATM resulted in a similar tumor-specific lethal effect, whereas the phenotype was reverted in rescue experiments. Conclusions: These six microRNAs might be developed as novel anti-cancer agents and highlight ATM as an interesting novel therapeutic target for head and neck cancer. Clin Cancer Res; 19(20); 5647–57. ©2013 AACR.

[1]  S. Gibbs,et al.  Adenovirus retargeting to surface expressed antigens on oral mucosa , 2010, The journal of gene medicine.

[2]  Igor Jurisica,et al.  Identification of a microRNA signature associated with progression of leukoplakia to oral carcinoma. , 2009, Human molecular genetics.

[3]  G. Snow,et al.  Biological evidence that human papillomaviruses are etiologically involved in a subgroup of head and neck squamous cell carcinomas , 2001, International journal of cancer.

[4]  A. Jemal,et al.  Global Cancer Statistics , 2011 .

[5]  J. Ferlay,et al.  Global Cancer Statistics, 2002 , 2005, CA: a cancer journal for clinicians.

[6]  Y. Yuzawa,et al.  In vivo silencing of a molecular target by short interfering RNA electroporation: tumor vascularization correlates to delivery efficiency , 2008, Molecular Cancer Therapeutics.

[7]  Y. Shiloh ATM and related protein kinases: safeguarding genome integrity , 2003, Nature Reviews Cancer.

[8]  Weihua Hu,et al.  Association between High miR-211 microRNA Expression and the Poor Prognosis of Oral Carcinoma , 2008, Journal of dental research.

[9]  M. Welters,et al.  Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma , 1996, Genes, chromosomes & cancer.

[10]  P. Pandolfi,et al.  A ceRNA Hypothesis: The Rosetta Stone of a Hidden RNA Language? , 2011, Cell.

[11]  D. Sidransky,et al.  Evidence for a causal association between human papillomavirus and a subset of head and neck cancers. , 2000, Journal of the National Cancer Institute.

[12]  Mariette Schrier,et al.  A Genetic Screen Implicates miRNA-372 and miRNA-373 As Oncogenes in Testicular Germ Cell Tumors , 2006, Cell.

[13]  N. Park,et al.  miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras. , 2011, Biochemical and biophysical research communications.

[14]  Yandan Yao,et al.  MiR-21 Indicates Poor Prognosis in Tongue Squamous Cell Carcinomas as an Apoptosis Inhibitor , 2009, Clinical Cancer Research.

[15]  W. Cho OncomiRs: the discovery and progress of microRNAs in cancers , 2007, Molecular Cancer.

[16]  A. Jemal,et al.  Global cancer statistics , 2011, CA: a cancer journal for clinicians.

[17]  C. Croce,et al.  miR-15 and miR-16 induce apoptosis by targeting BCL2. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[18]  D. Bartel,et al.  The impact of microRNAs on protein output , 2008, Nature.

[19]  Elisabeth Bloemena,et al.  A noninvasive genetic screening test to detect oral preneoplastic lesions , 2005, Laboratory Investigation.

[20]  Y Taya,et al.  Activation of the ATM kinase by ionizing radiation and phosphorylation of p53. , 1998, Science.

[21]  C. R. Leemans,et al.  Genetic patterns in head and neck cancers that contain or lack transcriptionally active human papillomavirus. , 2004, Journal of the National Cancer Institute.

[22]  K. Coombes,et al.  miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue , 2009, Head & neck.

[23]  W. Krzyzosiak,et al.  Practical Aspects of microRNA Target Prediction , 2011, Current molecular medicine.

[24]  W. Filipowicz,et al.  Regulation of mRNA translation and stability by microRNAs. , 2010, Annual review of biochemistry.

[25]  D. Brachman,et al.  Molecular biology of head and neck cancer. , 1994, Seminars in oncology.

[26]  R. Brakenhoff,et al.  Immortalization of oral keratinocytes by functional inactivation of the p53 and pRb pathways , 2011, International journal of cancer.

[27]  Thomas D. Schmittgen,et al.  Analyzing real-time PCR data by the comparative CT method , 2008, Nature Protocols.