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Cell-to-Cell Variation in p53 Dynamics Leads to Fractional Killing.

Paek, Andrew L. ; Liu, Julia C. ; Loewer, Alexander ; Forrester, William C. ; Lahav, Galit (2016)
Cell-to-Cell Variation in p53 Dynamics Leads to Fractional Killing.
In: Cell, 165 (3)
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

Many chemotherapeutic drugs kill only a fraction of cancer cells, limiting their efficacy. We used live-cell imaging to investigate the role of p53 dynamics in fractional killing of colon cancer cells in response to chemotherapy. We found that both surviving and dying cells reach similar levels of p53, indicating that cell death is not determined by a fixed p53 threshold. Instead, a cell's probability of death depends on the time and levels of p53. Cells must reach a threshold level of p53 to execute apoptosis, and this threshold increases with time. The increase in p53 apoptotic threshold is due to drug-dependent induction of anti-apoptotic genes, predominantly in the inhibitors of apoptosis (IAP) family. Our study underlines the importance of measuring the dynamics of key players in response to chemotherapy to determine mechanisms of resistance and optimize the timing of combination therapy.

Typ des Eintrags: Artikel
Erschienen: 2016
Autor(en): Paek, Andrew L. ; Liu, Julia C. ; Loewer, Alexander ; Forrester, William C. ; Lahav, Galit
Art des Eintrags: Bibliographie
Titel: Cell-to-Cell Variation in p53 Dynamics Leads to Fractional Killing.
Sprache: Englisch
Publikationsjahr: 2016
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Cell
Jahrgang/Volume einer Zeitschrift: 165
(Heft-)Nummer: 3
Kurzbeschreibung (Abstract):

Many chemotherapeutic drugs kill only a fraction of cancer cells, limiting their efficacy. We used live-cell imaging to investigate the role of p53 dynamics in fractional killing of colon cancer cells in response to chemotherapy. We found that both surviving and dying cells reach similar levels of p53, indicating that cell death is not determined by a fixed p53 threshold. Instead, a cell's probability of death depends on the time and levels of p53. Cells must reach a threshold level of p53 to execute apoptosis, and this threshold increases with time. The increase in p53 apoptotic threshold is due to drug-dependent induction of anti-apoptotic genes, predominantly in the inhibitors of apoptosis (IAP) family. Our study underlines the importance of measuring the dynamics of key players in response to chemotherapy to determine mechanisms of resistance and optimize the timing of combination therapy.

Fachbereich(e)/-gebiet(e): 10 Fachbereich Biologie
10 Fachbereich Biologie > Systems Biology of the Stress Response
Hinterlegungsdatum: 19 Mai 2016 07:14
Letzte Änderung: 19 Mai 2016 07:14
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