But, our klotho silencing results may eliminate this possibility. Though having no statistically significant selleck inhibitor change, the apoptosis of A549 cells tend to decrease after knockdown of klotho. And the changes of apoptosis-related genes bax/bcl-2 also supported that klotho may promote apoptosis of A549 cells. All these results suggested that the expression levels of anti-apoptotic bcl-2
decreased and pro-apoptotic bax increased, which might play a key role in klotho-induced apoptosis in the A549 cells. Conclusions In summary, klotho, a potential tumor suppressor, can inhibit the growth of lung cancer cells A549 and promote their apoptosis, this may be partly due to the inhibition of IGF-1/insulin pathways and involving regulating the expression of the apoptosis-related genes bax/bcl-2. The function of klotho is very complex, and the signal pathways in cancer development are interwound and cross-linking, so the exact role and working mechanisms of klotho in vitro and in vivo are still waiting to be explored. Further study of the biological functions of klotho may be helpful in developing new strategies in lung cancer treatment.
Acknowledgements This work was partly supported by the grants from the National Natural Science Foundation of China (No. 30971320), Foundation of Jiangsu Key Researchers in Medical Science (RC2007051), and Foundation of Jiangsu Health Department in Scientific Research (P200904). References 1. Jemal Janus kinase (JAK) A, Siegel
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