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Emerging role of small ribonucleic acids in gastrointestinal tumors

Iuliana ShapiraaCorresponding Author Informationemail address, Keith Sultanb1email address, Bhoomi Mehrotrac2email address, Daniel R. Budmand3email address

Accepted 27 January 2010. published online 08 February 2010.
Corrected Proof

Abstract 

Small regulatory ribonucleic acids (RNAs) are recently recognized as being connected with a growing list of common diseases such as: cancer, heart disease, diabetes and inflammation and to date more than 5,000 publications are recorded on PubMed alone. Specific pathways generate each class of RNAs and their activities converge in the process of silence interference.

In gastrointestinal malignancies microRNAs are deregulated, sometimes found in higher or lower levels depending on the type of malignancy and stage of the disease, functioning either as tumor suppressors or as oncogenes they interact forming regulatory loops with known transcription factors and signaling pathways. MiRNAs extracted from archived tissue biopsies can be used effectively as diagnostic, prognostic tools and molecular markers because they are stable over time and resistant to RNAse degradation. The distinct physiology of small RNAs may translate in more targeted cancer therapies in the near future.

a Hematology Oncology, Hofstra University School of Medicine, Monter Cancer Center, 450 Lakeville Road, Lake Success, NY 11042, USA

b Hofstra University School of Medicine, Division of Gastroenterology Hepatology and Nutrition, North Shore University Hospital, 300 Community Drive, Manhasset, NY 11030, USA

c Hofstra University School of Medicine, Hematology Oncology, Monter Cancer Center, 450 Lakeville Road, Lake Success, NY 11042, USA

d Hofstra University School of Medicine, Don Monti Division of Oncology, Monter Cancer Center of North Shore University Hospital, 450 Lakeville Road, Lake Success, NY 11042, USA

Corresponding Author InformationCorresponding author. Tel.: +1 516 734 8964; fax: +1 516 734 8950.

1 Tel.: +1 516 562 4281; fax: +1 516 562 2683.

2 Tel.: +1 516 734 8963; fax: +1 516 734 8924.

3 Tel.: +1 516 734 8958; fax: +1 516 734 8924.

PII: S1040-8428(10)00028-4

doi:10.1016/j.critrevonc.2010.01.013