The transcription factor, Nrf2, has emerged as the master regulator of a cellular protective mechanism by upregulating antioxidant response element (ARE)- bearing genes encoding antioxidant enzymes, detoxifying enzymes, xenobiotic transporters, and stress response proteins. Very recently, mounting evidence points to the dual function of Nrf2 in cancer. (i) In normal cells when the Nrf2- Keap1 axis is intact and basal level of Nrf2 are low, transient activation of Nrf2 by chemopreventive compounds confers protection against environmental toxins and carcinogens. (ii) In certain cancer cell lines, constitutive activation of Nrf2 creates an environment conducive for cancer cell survival. Moreover, Nrf2 contributes to chemoresistance and inhibition of the Nrf2 pathway enhances the efficacy of cancer treatments. Arsenic (As) is a human carcinogen, which causes tumors in the skin, lung and bladder. Large populations around the world are exposed to arsenic through contaminated drinking water, which imposes a major challenge to human health. However, a sufficient rodent model to study arsenic-carcinogenicity is still lacking. This competing renewal of NIH ES015010 takes advantage of a previously unrecognized role of arsenic in autophagy leading to prolonged activation of Nrf2, which was uncovered during the last funding period. We hypothesize that arsenic-mediated carcinogenicity is associated with its ability to deregulate the autophagic pathway. We believe that canonical Nrf2 inducers can alleviate this effect and thus, can be used as chemopreventive agents to counteract the damaging effects of arsenic. The following three aims are proposed:
Aim 1 (in vitro): Elucidate a novel mechanism of Nrf2 induction by arsenic through deregulation of autophagy (prolonged activation of Nrf2).
Aim 2 (ex vivo): Determine the role of Nrf2 in arsenic-mediated autophagosome formation and carcinogenicity using a transplantable syngeneic mouse lung cancer model.
Aim 3 (in vivo): Validate the biological and pharmacological relevancy of this work. From this proposal we will (i) gain novel mechanistic insight of how arsenic deregulates autophagy, (ii) confirm the association between deregulation of autophagy and tumorigenicity of arsenic, (iii) provide new biomarkers and a sensitive animal model for arsenic carcinogenicity studies and (iv) demonstrate the potential translational impact of targeting the Nrf2 pathway using canonical Nrf2 activators to combat arsenic-induced toxicity and carcinogenicity. In addition, the syngeneic mouse lung cancer model developed will be invaluable for scientific communities studying other carcinogens.
Arsenic (As) is a human carcinogen, however, a sufficient rodent model to study arsenic-carcinogenicity is still lacking. This competing renewal of NIH ES015010 takes advantage of a previously unrecognized role of As in autophagy, which was uncovered during the last funding period. We hypothesize that As-mediated carcinogenicity is associated with its ability to deregulate the autophagic pathway. Consequently, we believe that canonical Nrf2 inducers can alleviate this effect and thus, can be used as chemopreventive agents to counteract the damaging effects of As. The translational value of this project is enormous based on the fact that large populations in the world are stilling drinking arsenic-contaminated water. As the saying goes, an ounce of prevention is worth a pound of cure. Furthermore, this proposed project will identify sensitive biomarkers for arsenic exposure, and develop a syngeneic mouse lung cancer model to study arsenic- carcinogenicity. In addition, this mouse model will be invaluable for scientific communities studying other carcinogens.
| Dodson, Matthew; Liu, Pengfei; Jiang, Tao et al. (2018) Increased O-GlcNAcylation of SNAP29 drives arsenic-induced autophagic dysfunction. Mol Cell Biol : |
| Tao, Shasha; Liu, Pengfei; Luo, Gang et al. (2017) p97 Negatively Regulates NRF2 by Extracting Ubiquitylated NRF2 from the KEAP1-CUL3 E3 Complex. Mol Cell Biol 37: |
| Dodson, Matthew; Zhang, Donna D (2017) Non-canonical activation of NRF2: New insights and its relevance to disease. Curr Pathobiol Rep 5:171-176 |
| Melo-Cardenas, Johanna; Zhang, Yusi; Zhang, Donna D et al. (2016) Ubiquitin-specific peptidase 22 functions and its involvement in disease. Oncotarget 7:44848-44856 |
| Rojo de la Vega, Montserrat; Dodson, Matthew; Gross, Christine et al. (2016) Role of Nrf2 and Autophagy in Acute Lung Injury. Curr Pharmacol Rep 2:91-101 |
| Tao, Shasha; Rojo de la Vega, Montserrat; Quijada, Hector et al. (2016) Bixin protects mice against ventilation-induced lung injury in an NRF2-dependent manner. Sci Rep 6:18760 |
| Long, Min; Rojo de la Vega, Montserrat; Wen, Qing et al. (2016) An Essential Role of NRF2 in Diabetic Wound Healing. Diabetes 65:780-93 |
| Rojo de la Vega, Montserrat; Dodson, Matthew; Chapman, Eli et al. (2016) NRF2-targeted therapeutics: New targets and modes of NRF2 regulation. Curr Opin Toxicol 1:62-70 |
| Long, Min; Tao, Shasha; Rojo de la Vega, Montserrat et al. (2015) Nrf2-dependent suppression of azoxymethane/dextran sulfate sodium-induced colon carcinogenesis by the cinnamon-derived dietary factor cinnamaldehyde. Cancer Prev Res (Phila) 8:444-54 |
| Wu, Tongde; Harder, Bryan G; Wong, Pak K et al. (2015) Oxidative stress, mammospheres and Nrf2-new implication for breast cancer therapy? Mol Carcinog 54:1494-502 |
Showing the most recent 10 out of 58 publications
