Activation of PKA leads to mesenchymal-to-epithelial transition and loss of tumor-initiating ability

Author:

Pattabiraman Diwakar R.1,Bierie Brian1,Kober Katharina Isabelle1,Thiru Prathapan1,Krall Jordan A.1,Zill Christina1,Reinhardt Ferenc1,Tam Wai Leong123,Weinberg Robert A.145

Affiliation:

1. Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

2. Genome Institute of Singapore, 60 Biopolis Street, Singapore.

3. Cancer Science Institute of Singapore, 14 Medical Drive, Singapore.

4. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

5. Ludwig Center for Molecular Oncology at MIT, Cambridge, MA 02142, USA.

Abstract

Have cancer stem cells MET their match? Solid tumors have been hypothesized to contain a subset of highly aggressive cells that fuel tumor growth and metastasis. The search is on for drugs that selectively kill or diminish the malignant properties of these tumor-initiating cells (TICs; previously called “cancer stem cells”). Pattabiraman et al. hypothesized that compounds that induce TICs to undergo a phenotypic change called the mesenchymal-to-epithelial transition (MET) would therefore cause TICs to lose their tumor-initiating ability. Indeed, drugs activating the protein kinase A signaling pathway triggered an epigenetic reprogramming of TICs that resulted in the cells acquiring a more benign epithelial-like phenotype. Science , this issue p. 10.1126/science.aad3680

Funder

National Health and Medical Research Council of Australia

National Research Foundation, Singapore

National Medical Research Council, Singapore

Ludwig Center for Molecular Oncology at MIT

Breast Cancer Research Foundation

Samuel Waxman Cancer Research Foundation

NIH

American Cancer Society

D. K. Ludwig Foundation Cancer Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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