More than 40 years ago, the phenomenon of "accelerated repopulation" was described in experimental tumors undergoing radiotherapy. Today, the concept of preventing tumor cellular repopulation during treatment is a basic tenet in radiotherapy. In fact, it is one of the four all-important "R"s widely taught in radiation oncology textbooks. However, the molecular mechanisms involved in tumor repopulation are still very poorly understood. In this project, we propose a paradigm changing hypothesis with regard to the molecular mechanism of tumor repopulation during radiotherapy. Our hypothesis is that dying cells are responsible for mobilizing and stimulating the surviving tumor cells to repopulate the irradiated tumor through paracrine signaling. Our hypothesis is based on our recent discovery of the "Phoenix Rising" pathway through which caspase 3 activates paracrine signaling cascades from dying cells to stimulate tissue regeneration and the rapid proliferation of surviving tumor cells in irradiated tumors. We plan to carry out the following in-depth investigations of the roles of caspases and other factors in the "Phoenix Rising" pathway in tumor response to radiotherapy (specific aim 1). In addition, we plan to examine the roles of downstream factors of caspases in the "Phoenix Pathway" (specific aim 2). Finally we will attempt to determine if inhibition of caspases or their downstream factors is a feasible strategy to enhance cancer radiotherapy (specific aim 3). We believe our project will provide crucial insights into how tumors relapse after radiotherapy. It also has the potential to facilitate the development of new therapeutics for enhancing cancer radiotherapy.
In this project, we seek to carry out a major re-definition of the roles of cell death in cancer radiotherapy. We will examine a counter-intuitive hypothesis that poses a direct challenge to the existing paradigm on the biological roles of apoptosis. If proven correct, we will gain significant biological insights as well as generating exciting ideas on developing novel approaches for enhancing cancer radiotherapy. Therefore, our project is highly translatable to the fields of cancer treatment and thus relevant to the mission of NCI.
|Liu, Xinjian; Zhou, Min; Mei, Ling et al. (2016) Key roles of necroptotic factors in promoting tumor growth. Oncotarget 7:22219-33|
|Li, Fang; Liu, Xinjian; Sampson, John H et al. (2016) Rapid Reprogramming of Primary Human Astrocytes into Potent Tumor-Initiating Cells with Defined Genetic Factors. Cancer Res 76:5143-50|
|Feng, Xiao; Tian, Ling; Zhang, Zhengxiang et al. (2015) Caspase 3 in dying tumor cells mediates post-irradiation angiogenesis. Oncotarget 6:32353-67|
|Liu, Xinjian; He, Yujun; Li, Fang et al. (2015) Caspase-3 promotes genetic instability and carcinogenesis. Mol Cell 58:284-96|
|Cheng, Jin; Tian, Ling; Ma, Jingjing et al. (2015) Dying tumor cells stimulate proliferation of living tumor cells via caspase-dependent protein kinase CÎ´ activation in pancreatic ductal adenocarcinoma. Mol Oncol 9:105-14|
|Liu, XinJian; Huang, Qian; Li, Fang et al. (2014) Enhancing the efficiency of direct reprogramming of human primary fibroblasts into dopaminergic neuron-like cells through p53 suppression. Sci China Life Sci 57:867-75|
|Liu, Chad; Li, Chuan-Yuan; Yuan, Fan (2014) Mathematical modeling of the Phoenix Rising pathway. PLoS Comput Biol 10:e1003461|
|Donato, Anne L; Huang, Qian; Liu, Xinjian et al. (2014) Caspase 3 promotes surviving melanoma tumor cell growth after cytotoxic therapy. J Invest Dermatol 134:1686-92|
|Ma, Jingjing; Tian, Ling; Cheng, Jin et al. (2013) Sonic hedgehog signaling pathway supports cancer cell growth during cancer radiotherapy. PLoS One 8:e65032|
|Ng, Wooi-Loon; Huang, Qian; Liu, Xinjian et al. (2013) Molecular mechanisms involved in tumor repopulation after radiotherapy. Transl Cancer Res 2:442-448|
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