Ount and Lixisenatide web morphological differences presented in photomicrographs (Figure 6). As shown in Figure 6A and 6B, the cells treated with modified sequence have noticeably fewer cells as compared with the scrambled sequence where there appears to be more cells per view and packed closely to one another. Furthermore, under the same magnification, the morphology of the cells treated with the modified sequence appears longer and thinner with many side projections as compared with the scrambled sequence, which are more angular and more defined in shape (Figure 6C and 6D). These findings indicate the potential of the PS-modified SL2-B aptamer sequence in inhibiting the Hep 12926553 G2 cancer cells proliferation strongly and specifically. To determine the cell death mechanism in Hep G2 cells, annexin V apoptosis assay was performed and analyzed using flow cytometry. In Figure 7A, the R9 and R11 quadrant cells in flow cytometry scatterplot were counted and expressed as percentage of cells in late and early apoptosis phase respectively. Early apoptotic cells include cell population that is annexin V positive only (R11),Antiproliferative Activity of Aptamer on Cancererative activity in Hep G2 cells not only by inhibiting VEGF pathway but also the interconnected delta/jagged-notch signaling pathway in Hep G2 cells. Further studies are warranted to determine the effect of the modified aptamer on different notch ligands and other VEGF linked signaling pathways.aptamer sequence can potentially be useful in oligomer-based cancer therapeutic applications, though further preTunicamycin site clinical studies are required for better understanding of the SL2-B aptamer sequence and to evaluate its potential therapeutic value for cancer treatment.ConclusionsTo summarize, this work attempted to study the antiproliferative potential of SL2-B aptamer in cancer cells. From the data, we conclude that post-modification, the PS-modified SL2-B aptamer retained its binding affinity and specificity for the heparin-binding domain (HBD) of VEGF165 protein. Furthermore, compared to the unmodified aptamer, the modified SL2-B demonstrated good biostability and exhibited its sequence 
specific antiproliferative activity on Hep G2 cancer cells in hypoxia conditions. Thus, based on the results of this work, it appears that chemical modification can be a useful approach in prolonging the half-life of the SL2-B aptamer in the in vitro conditions. This newly obtained SL2-BAcknowledgmentsThe authors 1516647 thank Dr Tong Yen Wah (Department of Chemical and Biomolecular engineering, National University of Singapore) for providing the Hep G2 cancer cells.Author ContributionsConceived and designed the experiments: HK JJL BHB LLY. Performed the experiments: HK JJL. Analyzed the data: HK JJL BHB LLY. Contributed reagents/materials/analysis tools: HK JJL LLY. Wrote the paper: HK JJL LLY.
Beta emitting radionuclides have found widespread use in cancer therapy. A major advance in nuclear medicine was the development of targeted endo-radiotherapies with two targeted radiotherapy agents approved for clinical use. BEXXARH, labeled with 131I, is used to treat follicular lymphoma while ZevalinH, containing 90Y, is used for treatment of B cell non-Hodgkins lymphoma [1?]. Other targeted radiotherapy agents labeled with b2 emitters 131I, 90Y, 177Lu, and 188Re are showing promise in ongoing clinical trials [3?]. One of the challenges associated with b2 emitting targeted radionuclide therapies is, however, the inherent toxicity from the de.Ount and morphological differences presented in photomicrographs (Figure 6). As shown in Figure 6A and 6B, the cells treated with modified sequence have noticeably fewer cells as compared with the scrambled sequence where there appears to be more cells per view and packed closely to one another. Furthermore, under the same magnification, the morphology of the cells treated with the modified sequence appears longer and thinner with many side projections as compared with the scrambled sequence, which are more angular and more defined in shape (Figure 6C and 6D). These findings indicate the potential of the 
PS-modified SL2-B aptamer sequence in inhibiting the Hep 12926553 G2 cancer cells proliferation strongly and specifically. To determine the cell death mechanism in Hep G2 cells, annexin V apoptosis assay was performed and analyzed using flow cytometry. In Figure 7A, the R9 and R11 quadrant cells in flow cytometry scatterplot were counted and expressed as percentage of cells in late and early apoptosis phase respectively. Early apoptotic cells include cell population that is annexin V positive only (R11),Antiproliferative Activity of Aptamer on Cancererative activity in Hep G2 cells not only by inhibiting VEGF pathway but also the interconnected delta/jagged-notch signaling pathway in Hep G2 cells. Further studies are warranted to determine the effect of the modified aptamer on different notch ligands and other VEGF linked signaling pathways.aptamer sequence can potentially be useful in oligomer-based cancer therapeutic applications, though further preclinical studies are required for better understanding of the SL2-B aptamer sequence and to evaluate its potential therapeutic value for cancer treatment.ConclusionsTo summarize, this work attempted to study the antiproliferative potential of SL2-B aptamer in cancer cells. From the data, we conclude that post-modification, the PS-modified SL2-B aptamer retained its binding affinity and specificity for the heparin-binding domain (HBD) of VEGF165 protein. Furthermore, compared to the unmodified aptamer, the modified SL2-B demonstrated good biostability and exhibited its sequence specific antiproliferative activity on Hep G2 cancer cells in hypoxia conditions. Thus, based on the results of this work, it appears that chemical modification can be a useful approach in prolonging the half-life of the SL2-B aptamer in the in vitro conditions. This newly obtained SL2-BAcknowledgmentsThe authors 1516647 thank Dr Tong Yen Wah (Department of Chemical and Biomolecular engineering, National University of Singapore) for providing the Hep G2 cancer cells.Author ContributionsConceived and designed the experiments: HK JJL BHB LLY. Performed the experiments: HK JJL. Analyzed the data: HK JJL BHB LLY. Contributed reagents/materials/analysis tools: HK JJL LLY. Wrote the paper: HK JJL LLY.
Beta emitting radionuclides have found widespread use in cancer therapy. A major advance in nuclear medicine was the development of targeted endo-radiotherapies with two targeted radiotherapy agents approved for clinical use. BEXXARH, labeled with 131I, is used to treat follicular lymphoma while ZevalinH, containing 90Y, is used for treatment of B cell non-Hodgkins lymphoma [1?]. Other targeted radiotherapy agents labeled with b2 emitters 131I, 90Y, 177Lu, and 188Re are showing promise in ongoing clinical trials [3?]. One of the challenges associated with b2 emitting targeted radionuclide therapies is, however, the inherent toxicity from the de.