Highlights
- •p53 limits the power of the proto-oncogene MYC to drive epidermal differentiation
- •Loss of p53 causes replication stress and mitotic slippage in human keratinocytes
- •p53 protects the proliferative potential of the keratinocyte stem cell compartment
- •Loss or mutation of p53 promotes human squamous differentiation and shedding
Summary
Tumor suppressor p53 is a major cellular guardian of genome integrity, and its inactivation is the most frequent genetic alteration in cancer, rising up to 80% in squamous cell carcinoma (SCC). By adapting the small hairpin RNA (shRNA) technology, we inactivated endogenous p53 in primary epithelial cells from the epidermis of human skin. We show that either loss of endogenous p53 or overexpression of a temperature-sensitive dominant-negative conformation triggers a self-protective differentiation response, resulting in cell stratification and expulsion. These effects follow DNA damage and exit from mitosis without cell division. p53 preserves the proliferative potential of the stem cell compartment and limits the power of proto-oncogene MYC to drive cell cycle stress and differentiation. The results provide insight into the role of p53 in self-renewal homeostasis and help explain why p53 mutations do not initiate skin cancer but increase the likelihood that cancer cells will appear.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
Received: May 6, 2014; Received in revised form: August 14, 2014; Accepted: October 3, 2014; Published Online: November 06, 2014
© 2014 The Authors. Published by Elsevier Inc. User rights governed by an Open Access license.
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