Analysis of TLR4 signaling and PI3K/Akt pathway activation in ren | 20950
Journal of Cell Science & Therapy

Journal of Cell Science & Therapy
Open Access

ISSN: 2157-7013

Analysis of TLR4 signaling and PI3K/Akt pathway activation in renal cancer cell line: A clinical approach

2nd World Congress on Cell Science & Stem Cell Research

November 12-14, 2012 Hilton San Antonio Airport, USA

Jatawa S K

Scientific Tracks Abstracts: J Cell Sci Ther

Abstract :

C ancer is uncontrolled growth of normal cells caused by a variety of genetic defects that occur in genes that encode for proteins involved in cell growth. There is a link between inflammation and cancer suggests that the mechanisms contributing to inflammation may also be critical for tumor formation. In present investigation, possible expression of TLR4 in renal cell lines of human, rabbit and rat has been tried to observe and finding demonstrate less expression of TLR4 noted in HEK293 cell lines while no expression observed in other two cell lines (NRK52E and RKK13). These findings suggest the possible role of inflammation in cancer. As LPS is a natural ligand for TLR4 activation there result is little bit controversial as compare to other studies similar to this but we know that LPS is natural component of bacteria those are responsible for various contamination but as we know kidney do not face any direct contact with bacterial infection so our finding is positively counterpart with the logic. These findings showed that TLR4 is possibly did not participate in renal cell carcinoma like other cancers viz . colorectal tumorigenesis and other cancers. On the other the phosphorylation of Akt, suggests that LPS related activity for Akt phosphorylation with all three cell lines but as the findings of PCR do not show any related activity of TLR4 with these cell lines. The development of renal cell carcinoma TLR4 did not play any direct role, alternatively Akt phosphorylation suggest there are certain other probable factor which may possibly alter the expression level. These factors are might be MyD88, activation of mTor pathway or cell proliferation process

Biography :

Mr. Suresh Kumar Jatawa has pursued Masters in Science (Biotechnology) in the year 2005 from Central University, Sagar, India. He is currently pursuing his doctoral studies at School of Biotechnology, Rajiv Gandhi Proudyogiki Vishwavidyalaya, Bhopal, India, in the field of Medical Biotechnology (Cancer Biology). He will be soon submitting his thesis for the award of degree. He has published more than 15 publications in well repute international and national journals