TAp73 is a structural homologue of the pre-eminent tumour suppressor p53. However, unlike p53, TAp73 is rarely mutated, and instead is frequently overexpressed in human tumours. It remains unclear whether TAp73 affords an advantage to tumour cells and if so, what the underlying mechanism is. Here we show that TAp73 supports the proliferation of human and mouse tumour cells. TAp73 activates the expression of glucose-6-phosphate dehydrogenase (G6PD), the rate-limiting enzyme of the pentose phosphate pathway (PPP). By stimulating G6PD, TAp73 increases PPP flux and directs glucose to the production of NADPH and ribose, for the synthesis of macromolecules and detoxification of reactive oxygen species (ROS). The growth defect of TAp73-deficient cells can be rescued by either enforced G6PD expression or the presence of nucleosides plus an ROS scavenger. These findings establish a critical role for TAp73 in regulating metabolism, and connect TAp73 and the PPP to oncogenic cell growth.
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We thank G. Melino (University Rome Tor Vergata, Rome, Italy), C. Chen (Albany Medical College, Albany, USA), A. Tullo (University of Rome La Sapienza, Rome, Italy), U. M. Moll (Stony Brook University, Stony Brook, New York, USA), M. C. Marín (Harvard Medical School, Boston, USA), B. Vogelstein (Johns Hopkins University, Baltimore, USA), W. El-Deiry (Penn State Hershey Cancer Institute, Pennsylvania, USA) for expression plasmids, antibodies and/or cell lines; W. Wang, Y. Mei, N. Li, X. Wang, W. Tan, E. Witze and K. E. Wellen for technical assistance; and C. O’Neill for help with manuscript preparation. Supported by China National Natural Science Foundation (31030046), Chinese Academy of Sciences (XDA01020104), Ministry of Science and Technology of China (2010CB912804 and 2011CB966302) and the Ministry of Education of China (20123402130006) to M.W., and US National Institutes of Health (CA088868 and GM060911) and the Department of Defense (W81XWH-10-1-0468) to X.Y.
The authors declare no competing financial interests.
Integrated supplementary information
(a) Schematic representation of p53 and the TAp73 and ΔNp73 isoform classes. Each p73 isoform class comprises various splicing variants (α, β, γ etc.) that differ in their C-terminal regions. TA: transactivation domain. DBD: DNA-binding domain. OD: oligomerization domain. SAM: sterile alpha motif. (b) TAp73+/+ and TAp73−/− MEF cells cultured for 4 days were stained with crystal violet. (c) Representative images of animals two weeks after injected with TAp73+/+ and TAp73−/− MEF cells. (d) U2OS cells stably expressing control or TAp73 shRNA were stained with crystal violet at day 6. (e,f) Proliferation of two independent clones of ΔNp73−/− and ΔNp73+/+ MEFs in culture and images of crystal violet staining at day 6. Data are means ± SD (n = 3 independent experiments).
(a) The pentose phosphate pathway and its link with glycolysis. FBP: fructose 1,6-biphosphate. PEP: phosphoenolpyruvate. TCA cycle: tricarboxylic acid cycle. (b) Expression of G6PD and TAp73 proteins in U2OS cells transfected with control siRNA or p73 siRNA, plus control vector or siRNA-resistant plasmid encoding Flag-TAp73. Western blots represent two independent experiments. (c) Semiquantitative RT-PCR analysis of ΔNp73 expression in HeLa, U2OS, H1299, and p53+/+ HCT116 cells. (d) Comparison of effect of p73 and ΔNp73 on G6PD expression in p73, ΔNp73 or control siRNA in HeLa cells by RT-PCR. (e) U2OS cells were infected with lentiviruses expressing a TAp73 shRNA or a control shRNA and cultured for the indicated time. The expression of G6PD, TAp73, and actin was analyzed by Western blot. The data represents three independent experiments. (f) mRNA expression in H1299 cells stably expressing control shRNA, p63 shRNA, or TAp73 shRNA was assayed by RT-PCR. (g) Quantitative RT-PCR analysis of G6PD expression in H1299 cells transfected with increasing amounts of control plasmid or plasmid expressing the indicated p53 family proteins. Data are means ± SD (n = 3 independent experiments). (h) A549 cells were treated with 1 μg/ml doxorubicin for 24 hour and protein expression was analyzed by Western blot. (i) Luciferase reporter assay of 293T cells transfected with p73 RE-luciferase construct or control construct, plus TAp73 or ΔNp73. Data are means ± SD (n = 3 independent experiments). (j) H1299 cells were transfected with increasing amounts of Flag-p53R175H, Flag-p53R273H, or Flag-TAp73α as indicated. Protein expression was examined by Western blot. The data represents two independent experiments.
(a,b) NADPH levels (a) and relative NADP+/NADPH ratios (b) in ΔNp73+/+ and ΔNp73−/− MEF cells. Data are means ± SD (n = 3 independent experiments). (c) Relative NADPH levels in IMR90 cells transfected with control (−) or p73 siRNA. Data are means ± SD (n = 3 independent experiments). (d) NADP+/NADPH ratios of IMR90 cells treated with p73 or control siRNA. Data are means ± SD (n = 3 independent experiments). (e) Relative NADPH levels in p53+/+ and p53−/− HCT116 cells transfected with control (−) or p73 siRNA. Data are means ± SD (n = 3 independent experiments).
(a) TAp73+/+ and TAp73−/− MEF cells treated with control or G6pd siRNA. ROS was measured by 2′, 7′-di-chlorofluorescein (DCF) staining and flow cytometry (left), and protein expression by Western blot (Right). Western blots represent three independent experiments. (b) ROS levels in TAp73+/+ and TAp73−/− MEF cells that were treated with or without DHEA. (c) IMR90 cells were transfected with p73, G6PD, and control siRNA as indicated. ROS was measured. (d) TAp73+/+ and TAp73−/− MEF cells were treated with or without 50 mM H2O2 for 30 min and then cultured for 24 h in the presence or absence of DHEA. Cell viability was analyzed. Data are means ± SD (n = 3 independent experiments). (e) U2OS cells were transfected with control siRNA (−), p73 siRNA, and G6PD siRNA as indicated. Cells were treated with or without 250 μM H2O2 for 24 h and cell viability was analyzed by trypan blue staining. Data are means ± SD (n = 3 independent experiments).
(a,b) p53−/− and p21−/− HCT116 cells were transfected with control (−), p73, and G6PD siRNA as indicated. Cells were assayed for BrdU incorporation. Data are means ± SD (n = 3 independent experiments). (c,d) Cell-cycle profile of p53−/− (c) and p21−/− (d) HCT116 cells transfected with p73, G6PD, and control siRNA as indicated. Protein expression is shown below. Western blots represent three independent experiments. (e) Percentage of SA- β-gal positive cells in IMR90 culture that were transfected with control, p73, or G6PD siRNA, and cultured for 72 h. Protein expression is shown below. Data are means ± SD (n = 3 independent experiments). Western blots represent three independent experiments.
(a–c) Proliferation of p53+/+ (a), p53−/− (b), and p21−/− (c) HCT116 cells transfected with the control, G6PD, and p73 siRNAs as indicated. Data are means ± SD (n = 3 independent experiments). (d) Growth of U2OS cells transfected with control siRNA or p73 siRNA, plus control vector or Flag-G6PD. Data are means ± SD (n = 3 independent experiments). Protein expression is shown on the Right. Western blots represent three independent experiments. (e–h) Growth of TAp73+/+ and TAp73−/− MEF cells stably overexpressing G6PD or vector control. Cells were cultured in medium containing vehicle (e), NAC (f), four ribonucleosides and four deoxyribonucleosides (Nuc) (g), or both NAC and Nuc (h). Data are means ± SD (n = 3 independent experiments).
Supplementary Figure 7 G6PD levels are associated with breast cancer metastasis and a role for G6PD and TAp73 in tumor growth.
(a,b) G6PD levels are associated with breast cancer metastasis. (a) Cox multivariable regression for metastasis risk using the indicated variables was performed on a cohort of 871 breast cancer patients. Shown are the hazard ratio (HR) and p-values. (b) Kaplan-Meier survival curves for metastasis-free survival. The patients were stratified by mean G6PD levels (‘hi’ is greater than mean, ‘lo’ is less than or equal to mean). P-value was determined by the log-rank test. (c) Representative images of animals three weeks after injected with TAp73+/+ and TAp73−/− MEF cells stably overexpressing G6PD or vector control. (d) Mice were injected with TAp73+/+ and TAp73−/− MEF cells that were treated with control or G6pd siRNA, and were fed with water containing no NAC or 40 mM NAC. Representative images of animals at three weeks are shown.
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Du, W., Jiang, P., Mancuso, A. et al. TAp73 enhances the pentose phosphate pathway and supports cell proliferation. Nat Cell Biol 15, 991–1000 (2013). https://doi.org/10.1038/ncb2789
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