iDentistry The Journal Volume 14 No.1 | Page 37

The Journal including several essential amino acids. The L- type amino acid transporter 1 (LAT1) is overexpressed to support cell growth in malignant tumors. Double-stranded RNA- mediated RNA interference (SiRNA) analysis can be used in a wide variety of eukaryotes to induce the sequence-specific inhibition of gene expression. In a current study RNAi has been found very successful for silencing LAT1 expression on the KB human oral squamous cell carcinoma. Steps in RNAi therapeutic development i. The initial step in this therapy is proper identification of the target gene which can be selected from various prime oncogenes, antiapoptotic genes or tumor promoting genes along with growth and angiogenic factors or their receptors. ii. The next step is the designing of siRNA sequences to achieve maximum efficiency. Adata processing algorithm that searches through the DNA or RNA sequences can be used for fulfilling the required criteria and displaying the resulting RNAi candidates ranked in their hierarchy of fit to the user supplied rule set(10). iii. Depending on the position and sequence of a given siRNA, specificity can be achieved. iv. The final step is the delivering of siRNA into the cells and organisms in a whole. Various successful delivery systems are available at present (refer fig.) viz. a) Direct delivery - Though it is a widely used technique yet it has less potentiality than the vector based delivery system. b) Vector based delivery - Both plasmid and viral vectors are technically more stable, potent and provide prolonged gene silencing. c) Nanoparticle based delivery system - It is one of the most recently proposed system which provide efficient specificity in the delivery of siRNA. In this technique large number of nanoparticles can be loaded into a protected environment followed by targeting them to the cancer cells which can be taken up efficiently by those cells and release RNA molecules into interior of the cells. Fig : siRNA delivery methods (GowharShafi) 36 Vol. 14 No. 1 Jan-Apr 2018