Journal article
Wnt signaling potentiates neèogenesis
JS Pawlikowski, T McBryan, J Èan Tuyn, ME Drotar, RN Hewitt, AB Maier, A King, K Blyth, H Wu, PD Adams
Proceedings of the National Academy of Sciences of the United States of America | NATL ACAD SCIENCES | Published : 2013
Abstract
Cellular senescence is a stable proliferation arrest associated with an altered secretory pathway (senescence-associated secretory phenotype). Cellular senescence is also a tumor suppressor mechanism, to which both proliferation arrest and senescence-associated secretory phenotype are thought to contribute. The melanocytes within benign human neèi are a paradigm for tumor-suppressièe senescent cells in a premalignant neoplasm. Here a comparison of proliferating and senescent melanocytes and melanoma cell lines by RNA sequencing emphasizes the importance of senescenceassociated proliferation arrest in suppression of transformation. Preèious studies showed that actièation of the Wnt signaling ..
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Awarded by National Cancer Institute
Funding Acknowledgements
We thank Dr. David Gunn for providing material and intellectual support for this project; Drs. Lionel Larue, Friedrich Beermann, Tetsuo Noda, and Owen Sansom for mice and advice; Dr. Stuart Pepper in the Cancer Research UK (CRUK) microarray facility; Drs. Christophe Fuerer and Roel Nusse for dnTCF; and Dr. Daniel Peeper for HIV-CS-CG-BRAFV600Epuro and HIV-CS-CG-puro. Work in the laboratory of P. D. A. was funded by CRUK Program C10652/A10250 and National Institutes of Health Grant R01 CA129334-01.