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A contemporary approach in treating pancreatic cancer with therapeutic MicroRNAs identified using computational appraoch.
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Cancer Science & Therapy

ISSN: 1948-5956

Open Access

A contemporary approach in treating pancreatic cancer with therapeutic MicroRNAs identified using computational appraoch.


5th World Congress on Cancer Therapy

September 28-30, 2015 Atlanta, USA

Jasjit K Banwait and Dhundy R Bastola

College of Information Science &Technology, University of Nebraska, USA

Posters-Accepted Abstracts: J Cancer Sci Ther

Abstract :

Cancer research has generated valuable body of knowledge about the mutations that play significant role in cell proliferation. These mutations have led to gain of function in oncogenes whereas detrimental loss of function in tumor suppressor genes. Pancreatic ductal adenocarcinoma (PDAC) is an aggressive and exceptionally fatal cancer. Only 6% of patients survive more than 5 years after diagnosis. Gemcitabine is the primary drug used to treat PDAC with a mere 6.8 month survival rate as monotherapy, and up to 11.1 months as combination therapy. A major barrier to PDAC treatment is that chemoresistance eventually renders conventional drug therapy ineffective. Hence, new, therapies are urgently needed to combat this deadly disease. Use of microRNA (miRNA) has recently emerged as a promising alternative therapeutic approach. These miRNAs are ~21 nucleotides long non-protein-coding RNAs that post-transcriptionally regulate gene expression through translational repression and/or mRNA degradation mechanism. Numerous studies support the role of miRNA dysregulation in the poor prognosis, resistance, invasion, metastasis, and epithelial�mesenchymal transition in PDAC. However, identifying new miRNAs that can treat PDAC and the mRNA(s) which are regulated to provide the therapeutic benefit remains a challenge. Several computational studies have been conducted to identify miRNAs and genes involved in PDAC. In this study, we developed a computational framework to integrate knowledgebases (miRNA-mRNA interaction, gene expression, biological process and metabolic pathway data) and identify candidate therapeutic miRNA(s). Our long-term goal is to facilitate the efficient discovery of novel therapeutic miRNA through computational approaches that build on biological insights and data.

Biography :

Email: jbanwait@unomaha.edu

Google Scholar citation report
Citations: 3968

Cancer Science & Therapy received 3968 citations as per Google Scholar report

Cancer Science & Therapy peer review process verified at publons

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