| Literature DB >> 27197176 |
Julie Giraud1, Laura M Failla2, Jean-Marc Pascussi1, Ebba L Lagerqvist1, Jérémy Ollier1, Pascal Finetti3, François Bertucci3, Chu Ya1, Imène Gasmi1, Jean-François Bourgaux4, Michel Prudhomme4, Thibault Mazard5, Imade Ait-Arsa5, Leila Houhou6, Daniel Birnbaum3, André Pélegrin5, Charles Vincent5, James G Ryall7, Dominique Joubert1, Julie Pannequin8, Frédéric Hollande9.
Abstract
Subpopulations of cancer stem-like cells (CSC) are thought to drive tumor progression and posttreatment recurrence in multiple solid tumors. However, the mechanisms that maintain stable proportions of self-renewing CSC within heterogeneous tumors under homeostatic conditions remain poorly understood. Progastrin is a secreted peptide that exhibits tumor-forming potential in colorectal cancer, where it regulates pathways known to modulate colon CSC behaviors. In this study, we investigated the role of progastrin in regulating CSC phenotype in advanced colorectal cancer. Progastrin expression and secretion were highly enriched in colon CSC isolated from human colorectal cancer cell lines and colon tumor biopsies. Progastrin expression promoted CSC self-renewal and survival, whereas its depletion by RNA interference-mediated or antibody-mediated strategies altered the homeostatic proportions of CSC cells within heterogeneous colorectal cancer tumors. Progastrin downregulation also decreased the frequency of ALDH(high) cells, impairing their tumor-initiating potential, and inhibited the high glycolytic activity of ALDH(high) CSC to limit their self-renewal capability. Taken together, our results show how colorectal CSC maintain their tumor-initiating and self-renewal capabilities by secreting progastrin, thereby contributing to the tumor microenvironment to support malignancy. Cancer Res; 76(12); 3618-28. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27197176 DOI: 10.1158/0008-5472.CAN-15-1497
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701