EMT is not required for lung metastasis but contributes to chemoresistance
EMT is not required for lung metastasis but contributes to chemoresistance
复制标题
DOI:
--
复制
发表时间:
2016
期刊:
影响因子:
--
通讯作者:
Kari R. Fischer;A. Durrans;Sharrell B Lee;J. Sheng;Fuhai Li;Stephen T. C. Wong;Hyejin Choi;Tina El Raye
中科院分区:
文献类型:
--
作者:
Kari R. Fischer;A. Durrans;Sharrell B Lee;J. Sheng;Fuhai Li;Stephen T. C. Wong;Hyejin Choi;Tina El Raye
The role of epithelial to mesenchymal transition (EMT) in metastasis is a longstanding source of controversy, largely due to an inability to monitor transient and reversible EMT phenotypes in vivo. We established an EMT lineage tracing system to monitor this process, using a mesenchymal-specific Cre-mediated fluorescent marker switch system in spontaneous breast-toUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms Correspondence to: Dingcheng Gao, dig2009@med.cornell.edu, Vivek Mittal, vim2010@med.cornell.edu. Author Contributions: D.G., K.R.F., and V.M. designed the experiments. K.R.F. and D.G. performed the experiments. A.D., S.L., H.C., T. E. R and S.R., provided technical support with experiments and animal work. L.T.V. and N.K.A. made critical comments to improve the study design. J.S., F.L., and S.W. performed RNA-sequencing analysis. J.T., and R.F.S. generated the Vim-Cre transgenic mice. K.R.F., D.G. and V.M. wrote and edited the manuscript with input from the other authors. All authors discussed the results and conclusions drawn from them. Competing financial interests: The authors declare no competing financial interests. HHS Public Access Author manuscript Nature. Author manuscript; available in PMC 2016 May 26. Published in final edited form as: Nature. 2015 November 26; 527(7579): 472–476. doi:10.1038/nature15748. A uhor M anscript