p53 Protects Cells from Death at the Heatstroke Threshold Temperature
When the core body temperature is higher than 40°C, life is threatened due to heatstroke. Tumor repressor p53 is required for heat-induced apoptosis at hyperthermia conditions (>41°C). However, its role in sub-heatstroke conditions (≤40°C) remains unclear. Here, we reveal that both zebrafish and...
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Published in: | Cell reports (Cambridge) Vol. 29; no. 11; pp. 3693 - 3707.e5 |
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Abstract | When the core body temperature is higher than 40°C, life is threatened due to heatstroke. Tumor repressor p53 is required for heat-induced apoptosis at hyperthermia conditions (>41°C). However, its role in sub-heatstroke conditions (≤40°C) remains unclear. Here, we reveal that both zebrafish and human p53 promote survival at 40°C, the heatstroke threshold temperature, by preventing a hyperreactive heat shock response (HSR). At 40°C, both Hsf1 and Hsp90 are activated. Hsf1 upregulates the expression of Hsc70 to trigger Hsc70-mediated protein degradation, whereas Hsp90 stabilizes p53 to repress the expression of Hsf1 and Hsc70, which prevents excessive HSR to maintain cell homeostasis. Under hyperthermia conditions, ATM is activated to phosphorylate p53 at S37, which increases BAX expression to induce apoptosis. Furthermore, growth of p53-deficient tumor xenografts, but not that of their p53+/+ counterparts, was inhibited by 40°C treatment. Our findings may provide a strategy for individualized therapy for p53-deficient cancers.
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•p53 promotes survival by preventing a hyperreactive heat shock response (HSR) at 40°C•Excessive HSC70-mediated protein degradation (hyperreactive HSR) causes death at 40°C•HSP90 stabilizes p53 without phosphorylation at S37 to repress HSR at 40°C•ATM phosphorylates p53 at S37 to induce apoptosis in hyperthermia conditions
Gong et al. report that in contrast to promoting apoptosis in hyperthermia conditions, both zebrafish and human tumor repressor p53 protect cells from death by preventing a hyperreactive heat shock response at 40°C, the heatstroke threshold temperature (HTT). They may provide a strategy for individualized therapy for p53-deficient cancers. |
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AbstractList | When the core body temperature is higher than 40°C, life is threatened due to heatstroke. Tumor repressor p53 is required for heat-induced apoptosis at hyperthermia conditions (>41°C). However, its role in sub-heatstroke conditions (≤40°C) remains unclear. Here, we reveal that both zebrafish and human p53 promote survival at 40°C, the heatstroke threshold temperature, by preventing a hyperreactive heat shock response (HSR). At 40°C, both Hsf1 and Hsp90 are activated. Hsf1 upregulates the expression of Hsc70 to trigger Hsc70-mediated protein degradation, whereas Hsp90 stabilizes p53 to repress the expression of Hsf1 and Hsc70, which prevents excessive HSR to maintain cell homeostasis. Under hyperthermia conditions, ATM is activated to phosphorylate p53 at S37, which increases BAX expression to induce apoptosis. Furthermore, growth of p53-deficient tumor xenografts, but not that of their p53
counterparts, was inhibited by 40°C treatment. Our findings may provide a strategy for individualized therapy for p53-deficient cancers. When the core body temperature is higher than 40°C, life is threatened due to heatstroke. Tumor repressor p53 is required for heat-induced apoptosis at hyperthermia conditions (>41°C). However, its role in sub-heatstroke conditions (≤40°C) remains unclear. Here, we reveal that both zebrafish and human p53 promote survival at 40°C, the heatstroke threshold temperature, by preventing a hyperreactive heat shock response (HSR). At 40°C, both Hsf1 and Hsp90 are activated. Hsf1 upregulates the expression of Hsc70 to trigger Hsc70-mediated protein degradation, whereas Hsp90 stabilizes p53 to repress the expression of Hsf1 and Hsc70, which prevents excessive HSR to maintain cell homeostasis. Under hyperthermia conditions, ATM is activated to phosphorylate p53 at S37, which increases BAX expression to induce apoptosis. Furthermore, growth of p53-deficient tumor xenografts, but not that of their p53+/+ counterparts, was inhibited by 40°C treatment. Our findings may provide a strategy for individualized therapy for p53-deficient cancers. [Display omitted] •p53 promotes survival by preventing a hyperreactive heat shock response (HSR) at 40°C•Excessive HSC70-mediated protein degradation (hyperreactive HSR) causes death at 40°C•HSP90 stabilizes p53 without phosphorylation at S37 to repress HSR at 40°C•ATM phosphorylates p53 at S37 to induce apoptosis in hyperthermia conditions Gong et al. report that in contrast to promoting apoptosis in hyperthermia conditions, both zebrafish and human tumor repressor p53 protect cells from death by preventing a hyperreactive heat shock response at 40°C, the heatstroke threshold temperature (HTT). They may provide a strategy for individualized therapy for p53-deficient cancers. When the core body temperature is higher than 40°C, life is threatened due to heatstroke. Tumor repressor p53 is required for heat-induced apoptosis at hyperthermia conditions (>41°C). However, its role in sub-heatstroke conditions (≤40°C) remains unclear. Here, we reveal that both zebrafish and human p53 promote survival at 40°C, the heatstroke threshold temperature, by preventing a hyperreactive heat shock response (HSR). At 40°C, both Hsf1 and Hsp90 are activated. Hsf1 upregulates the expression of Hsc70 to trigger Hsc70-mediated protein degradation, whereas Hsp90 stabilizes p53 to repress the expression of Hsf1 and Hsc70, which prevents excessive HSR to maintain cell homeostasis. Under hyperthermia conditions, ATM is activated to phosphorylate p53 at S37, which increases BAX expression to induce apoptosis. Furthermore, growth of p53-deficient tumor xenografts, but not that of their p53+/+ counterparts, was inhibited by 40°C treatment. Our findings may provide a strategy for individualized therapy for p53-deficient cancers. : Gong et al. report that in contrast to promoting apoptosis in hyperthermia conditions, both zebrafish and human tumor repressor p53 protect cells from death by preventing a hyperreactive heat shock response at 40°C, the heatstroke threshold temperature (HTT). They may provide a strategy for individualized therapy for p53-deficient cancers. Keywords: p53, heatstroke threshold temperature, hyperthermia temperature, cell death, Hsf1, Hsc70, Hsp90, ATM, zebrafish, human cell |
Author | Feng, Xin-Hua Yuan, Zhi-Min Gong, Lu Zhang, Qinghe Wang, Haihe Chen, Jun Xiao, Zhi-Xiong Yang, Weijun Tan, Wei-Qiang Yang, Lina Liu, Bin Pan, Xiao Yu, Luyang Chen, Shuming Peng, Jinrong |
Author_xml | – sequence: 1 givenname: Lu surname: Gong fullname: Gong, Lu organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 2 givenname: Qinghe surname: Zhang fullname: Zhang, Qinghe organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 3 givenname: Xiao surname: Pan fullname: Pan, Xiao organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 4 givenname: Shuming surname: Chen fullname: Chen, Shuming organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 5 givenname: Lina surname: Yang fullname: Yang, Lina organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 6 givenname: Bin surname: Liu fullname: Liu, Bin organization: Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, 74 Second Zhonshan Road, Guangzhou 510080, China – sequence: 7 givenname: Weijun surname: Yang fullname: Yang, Weijun organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 8 givenname: Luyang surname: Yu fullname: Yu, Luyang organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China – sequence: 9 givenname: Zhi-Xiong surname: Xiao fullname: Xiao, Zhi-Xiong organization: Center of Growth, Metabolism and Aging, College of Life Sciences, Sichuan University, Chengdu 610064, China – sequence: 10 givenname: Xin-Hua surname: Feng fullname: Feng, Xin-Hua organization: Life Sciences Institute and Innovation Center for Signaling Network, Zhejiang University, 866 Yu Hang Tang Road, Hangzhou 310058, China – sequence: 11 givenname: Haihe surname: Wang fullname: Wang, Haihe organization: Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, 74 Second Zhonshan Road, Guangzhou 510080, China – sequence: 12 givenname: Zhi-Min surname: Yuan fullname: Yuan, Zhi-Min organization: Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115, USA – sequence: 13 givenname: Jinrong surname: Peng fullname: Peng, Jinrong organization: College of Animal Sciences, Zhejiang University, 866 Yu Hang Tang Road, Hangzhou 310058, China – sequence: 14 givenname: Wei-Qiang surname: Tan fullname: Tan, Wei-Qiang email: tanweixxxx@zju.edu.cn organization: Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, No. 3 Qingchun Road East, Hangzhou 310016, China – sequence: 15 givenname: Jun surname: Chen fullname: Chen, Jun email: chenjun2009@zju.edu.cn organization: MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou 310058, China |
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Keywords | Hsp90 cell death Hsf1 hyperthermia temperature ATM human cell heatstroke threshold temperature zebrafish Hsc70 p53 |
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SubjectTerms | ATM cell death heatstroke threshold temperature Hsc70 Hsf1 Hsp90 human cell hyperthermia temperature p53 zebrafish |
Title | p53 Protects Cells from Death at the Heatstroke Threshold Temperature |
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