Emerging evidences studying different types of cancer have revealed a relatively rare population of so called ''cancer stem cells''(CSCs), also known as "tumor-initiating cells" (TICs), which share certain characteristics with normal stem cells, including a stem cell-like phenotype and function. However, little is known about the signaling networks that control and regulate the function of the TICs, particularly those that influence their cell growth properties in a normal or an inflammatory microenvironment. Also, intratumoral nutrient stress has been found even in early-stage cancers, and is correlated with poor patient survival. Therefore, understanding the signaling mechanisms governing cancer stem cell proliferation under inflammation and nutrient stress is of paramount importance for the identification of new and more selective therapeutic targets in cancer. In this proposal we will investigate the signaling and metabolic pathways that regulate the growth properties of TICs in vitro and in a relevant in vivo mouse cancer model. Signaling molecules that promote the survival of TICs will be promising tumor suppressor candidates. This project will investigate the metabolism reprogramming of TICs in the framework of a novel signaling pathway controlled by PKC?. Our preliminary results show that PKC? represses cell growth of human colorectal cancer cells under nutrient stress conditions, and that it plays a tumor suppressive role in a mouse model of intestinal carcinogenesis driven by APC mutation. Also the loss o of PKC? results in increased stem cell activity in the intestine in vivo and in organoids. Furthermore, PKC? is absent, or underexpressed, in several types of human cancers, including colorectal neoplasias. This is significant because colorectal cancer is one of the most prevalent neoplasias, affecting a large portion of the US population. Therefore, understanding how TICs are regulated by PKC? will be of relevant for a better understanding of tumor initiation and the identification of potentially novel therapeutic targets. Therefore, we will: (1) Characterize the rle of PKC? in cancer stem cell expansion and the effect of PKC?-controlled inflammatory signals in the tumor microenvironment;and (2) Determine the role of PKC? in cancer stem cell proliferative signaling focusing in the control of cancer cell metabolism. In summary, here we will rigorously test the hypothesis that PKC? ablation in the intestinal stem cells would account for the initiation factors increasing the number and proliferative activity of TICs. Therefore, a bette understanding of the signaling cascades that regulate cancer stem cell signaling would be of great impact as it will aid in the design of new more efficacious and selective therapies.
Cancer stem cells or tumor-initiating cells (TICs) are a small population of cells that possess the ability to self-renew and to cause the heterogeneous lineages of cancer cells that comprise the tumor. This concept has important therapeutic implications because TICs are more resistant to the conventional cancer treatments and could be responsible for tumor relapse. The goal of this proposal is to determine the role of PKC? signaling in the growth properties of TICs in intestinal tumorigenesis under inflammation and nutrient stress. This proposal if successful will have a major impact on our understanding of the signaling cascades activated during tumor initiation in the stem cell populations and can yield new therapeutic approaches and novel targets for treating colon cancer.
|Moscat, Jorge; Karin, Michael; Diaz-Meco, Maria T (2016) p62 in Cancer: Signaling Adaptor Beyond Autophagy. Cell 167:606-609|
|Calero-Cuenca, Francisco J; Espinosa-VÃ¡zquez, JosÃ© Manuel; Reina-Campos, Miguel et al. (2016) Nuclear fallout provides a new link between aPKC and polarized cell trafficking. BMC Biol 14:32|
|Umemura, Atsushi; He, Feng; Taniguchi, Koji et al. (2016) p62, Upregulated during Preneoplasia, Induces Hepatocellular Carcinogenesis by Maintaining Survival of Stressed HCC-Initiating Cells. Cancer Cell 29:935-48|
|Duran, Angeles; Hernandez, Eloy D; Reina-Campos, Miguel et al. (2016) p62/SQSTM1 by Binding to Vitamin D Receptor Inhibits Hepatic Stellate Cell Activity, Fibrosis, and Liver Cancer. Cancer Cell 30:595-609|
|Nakanishi, Yuki; Reina-Campos, Miguel; Nakanishi, Naoko et al. (2016) Control of Paneth Cell Fate, Intestinal Inflammation, and Tumorigenesis by PKCÎ»/Î¹. Cell Rep 16:3297-310|
|Pan, Ji-An; Sun, Yu; Jiang, Ya-Ping et al. (2016) TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis. Mol Cell 61:720-33|
|Zhong, Zhenyu; Umemura, Atsushi; Sanchez-Lopez, Elsa et al. (2016) NF-ÎºB Restricts Inflammasome Activation via Elimination of Damaged Mitochondria. Cell 164:896-910|
|Moscat, Jorge; Richardson, Adam; Diaz-Meco, Maria T (2015) Nutrient stress revamps cancer cell metabolism. Cell Res 25:537-8|
|Linares, Juan F; Duran, Angeles; Reina-Campos, Miguel et al. (2015) Amino Acid Activation of mTORC1 by a PB1-Domain-Driven Kinase Complex Cascade. Cell Rep 12:1339-52|
|Llado, Victoria; Nakanishi, Yuki; Duran, Angeles et al. (2015) Repression of Intestinal Stem Cell Function and Tumorigenesis through Direct Phosphorylation of Î²-Catenin and Yap by PKCÎ¶ Cell Rep :|
Showing the most recent 10 out of 13 publications