Ke Wu, Xiaoting Yu, Xianghua Yi, Lynn Ma, Y. Elshimali, Yanjun Liu, Donghui Zhu, Yong Wu, J. Vadgama
{"title":"摘要:高糖通过上调PP2Cδ诱导乳腺癌进展","authors":"Ke Wu, Xiaoting Yu, Xianghua Yi, Lynn Ma, Y. Elshimali, Yanjun Liu, Donghui Zhu, Yong Wu, J. Vadgama","doi":"10.1158/1538-7755.DISP17-B76","DOIUrl":null,"url":null,"abstract":"Breast cancer has a high incidence worldwide. African-American and Hispanic/Latina women have higher mortality from breast cancer than other ethnic groups. Epidemiologic evidence suggests that women with diabetes have increased risk of breast cancer. Diabetes and cancer share many risk factors, but the pathophysiologic relationship between the two diseases is incompletely understood in detail. We observed that exposure of cultured transformed (MCF-7) and normal (MCF-12A) breast epithelial cells to clinically relevant levels of glucose (HG, 22 mM) dramatically suppresses the tumor suppressor p53 acetylation, and, consequently, additively promotes tumor cell proliferation, migration, and invasion. Importantly, we found that activation of nuclear phosphatase PP2Cδ (Ppm1d, WIP1) plays a role in the enhancing effects of HG on aggressive phenotypes of these cells. The mechanisms underlying high-glucose stimulation of PP2Cδ involve classical/novel PKCs activation and its downstream target protein GSK3β phosphorylation and inactivation. In addition, HG-induced reactive oxygen species (ROS) generation and subsequent NF-κB activation play a partial role in HG induction of PP2Cδ. HG inhibition of p53 activity and DNA damage-induced apoptosis, as well as induction of cancer cell proliferation, migration, and invasion, were significantly blocked by CCT007093, a known PP2Cδ inhibitor. We conclude that hyperglycemia, via PKC/GSK3β and ROS/NF-κB pathways that are involved in PP2Cδ activation, suppresses the tumor suppressor p53 function and inhibits DNA damage-induced apoptosis, inducing proliferation in the epithelium and the development of breast cancer. Citation Format: Ke Wu, Xiaoting Yu, Xianghua Yi, Lynn Ma, Yahya Elshimali, Yanjun Liu, Donghui Zhu, Yong Wu, Jaydutt V. Vadgama. High glucose induces breast cancer progression through upregulating PP2Cδ [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr B76.","PeriodicalId":146931,"journal":{"name":"Cell, Molecular, and Tumor Biology","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abstract B76: High glucose induces breast cancer progression through upregulating PP2Cδ\",\"authors\":\"Ke Wu, Xiaoting Yu, Xianghua Yi, Lynn Ma, Y. Elshimali, Yanjun Liu, Donghui Zhu, Yong Wu, J. Vadgama\",\"doi\":\"10.1158/1538-7755.DISP17-B76\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Breast cancer has a high incidence worldwide. African-American and Hispanic/Latina women have higher mortality from breast cancer than other ethnic groups. Epidemiologic evidence suggests that women with diabetes have increased risk of breast cancer. Diabetes and cancer share many risk factors, but the pathophysiologic relationship between the two diseases is incompletely understood in detail. We observed that exposure of cultured transformed (MCF-7) and normal (MCF-12A) breast epithelial cells to clinically relevant levels of glucose (HG, 22 mM) dramatically suppresses the tumor suppressor p53 acetylation, and, consequently, additively promotes tumor cell proliferation, migration, and invasion. Importantly, we found that activation of nuclear phosphatase PP2Cδ (Ppm1d, WIP1) plays a role in the enhancing effects of HG on aggressive phenotypes of these cells. The mechanisms underlying high-glucose stimulation of PP2Cδ involve classical/novel PKCs activation and its downstream target protein GSK3β phosphorylation and inactivation. In addition, HG-induced reactive oxygen species (ROS) generation and subsequent NF-κB activation play a partial role in HG induction of PP2Cδ. HG inhibition of p53 activity and DNA damage-induced apoptosis, as well as induction of cancer cell proliferation, migration, and invasion, were significantly blocked by CCT007093, a known PP2Cδ inhibitor. We conclude that hyperglycemia, via PKC/GSK3β and ROS/NF-κB pathways that are involved in PP2Cδ activation, suppresses the tumor suppressor p53 function and inhibits DNA damage-induced apoptosis, inducing proliferation in the epithelium and the development of breast cancer. Citation Format: Ke Wu, Xiaoting Yu, Xianghua Yi, Lynn Ma, Yahya Elshimali, Yanjun Liu, Donghui Zhu, Yong Wu, Jaydutt V. Vadgama. High glucose induces breast cancer progression through upregulating PP2Cδ [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. 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引用次数: 0
摘要
乳腺癌在世界范围内发病率很高。非裔美国人和西班牙裔/拉丁裔妇女患乳腺癌的死亡率高于其他族裔。流行病学证据表明,患有糖尿病的女性患乳腺癌的风险增加。糖尿病和癌症有许多共同的危险因素,但两种疾病之间的病理生理关系尚不完全清楚。我们观察到,将培养的转化(MCF-7)和正常(MCF-12A)乳腺上皮细胞暴露于临床相关水平的葡萄糖(HG, 22 mM)下,可显著抑制肿瘤抑制因子p53乙酰化,从而促进肿瘤细胞的增殖、迁移和侵袭。重要的是,我们发现核磷酸酶PP2Cδ (Ppm1d, WIP1)的激活在HG对这些细胞侵袭性表型的增强作用中起作用。高糖刺激PP2Cδ的机制涉及经典/新型PKCs激活及其下游靶蛋白GSK3β磷酸化和失活。此外,HG诱导的活性氧(ROS)生成和随后的NF-κB活化在PP2Cδ诱导HG中起部分作用。HG对p53活性和DNA损伤诱导的细胞凋亡的抑制作用以及对癌细胞增殖、迁移和侵袭的诱导作用被已知的PP2Cδ抑制剂CCT007093显著阻断。我们认为,高血糖通过参与PP2Cδ活化的PKC/GSK3β和ROS/NF-κB通路,抑制肿瘤抑制因子p53功能,抑制DNA损伤诱导的细胞凋亡,诱导上皮细胞增殖和乳腺癌的发生。引用格式:吴珂,余晓婷,易向华,马琳,叶海亚,刘彦军,朱东辉,吴勇,Jaydutt V. Vadgama。高糖通过上调PP2Cδ诱导乳腺癌进展[摘要]。见:第十届AACR会议论文集:种族/少数民族和医疗服务不足人群的癌症健康差异科学;2017年9月25-28日;亚特兰大,乔治亚州。费城(PA): AACR;癌症流行病学杂志,2018;27(7增刊):摘要nr B76。
Abstract B76: High glucose induces breast cancer progression through upregulating PP2Cδ
Breast cancer has a high incidence worldwide. African-American and Hispanic/Latina women have higher mortality from breast cancer than other ethnic groups. Epidemiologic evidence suggests that women with diabetes have increased risk of breast cancer. Diabetes and cancer share many risk factors, but the pathophysiologic relationship between the two diseases is incompletely understood in detail. We observed that exposure of cultured transformed (MCF-7) and normal (MCF-12A) breast epithelial cells to clinically relevant levels of glucose (HG, 22 mM) dramatically suppresses the tumor suppressor p53 acetylation, and, consequently, additively promotes tumor cell proliferation, migration, and invasion. Importantly, we found that activation of nuclear phosphatase PP2Cδ (Ppm1d, WIP1) plays a role in the enhancing effects of HG on aggressive phenotypes of these cells. The mechanisms underlying high-glucose stimulation of PP2Cδ involve classical/novel PKCs activation and its downstream target protein GSK3β phosphorylation and inactivation. In addition, HG-induced reactive oxygen species (ROS) generation and subsequent NF-κB activation play a partial role in HG induction of PP2Cδ. HG inhibition of p53 activity and DNA damage-induced apoptosis, as well as induction of cancer cell proliferation, migration, and invasion, were significantly blocked by CCT007093, a known PP2Cδ inhibitor. We conclude that hyperglycemia, via PKC/GSK3β and ROS/NF-κB pathways that are involved in PP2Cδ activation, suppresses the tumor suppressor p53 function and inhibits DNA damage-induced apoptosis, inducing proliferation in the epithelium and the development of breast cancer. Citation Format: Ke Wu, Xiaoting Yu, Xianghua Yi, Lynn Ma, Yahya Elshimali, Yanjun Liu, Donghui Zhu, Yong Wu, Jaydutt V. Vadgama. High glucose induces breast cancer progression through upregulating PP2Cδ [abstract]. In: Proceedings of the Tenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2017 Sep 25-28; Atlanta, GA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2018;27(7 Suppl):Abstract nr B76.