C. Gaillochet and J. U. Lohmann, The never-ending story: from pluripotency to plant developmental plasticity, Development, vol.142, pp.2237-2286, 2015.
DOI : 10.1242/dev.117614

URL : http://dev.biologists.org/content/develop/142/13/2237.full.pdf

C. Blanpain and E. Fuchs, Stem cell plasticity. Plasticity of epithelial stem cells in tissue regeneration, Science, vol.344, p.1242281, 2014.

G. Donati and F. M. Watt, Stem cell heterogeneity and plasticity in epithelia, Cell Stem Cell, vol.16, pp.465-76, 2015.
DOI : 10.1016/j.stem.2015.04.014

URL : https://doi.org/10.1016/j.stem.2015.04.014

J. E. Visvader and H. Clevers, Tissue-specific designs of stem cell hierarchies, Nat Cell Biol, vol.18, pp.349-55, 2016.
DOI : 10.1038/ncb3332

P. W. Tetteh, H. F. Farin, and H. Clevers, Plasticity within stem cell hierarchies in mammalian epithelia, Trends Cell Biol, vol.25, pp.100-108, 2015.
DOI : 10.1016/j.tcb.2014.09.003

C. Moyret-lalle, R. Pommier, and C. Bouard, Plasticité des cellules cancéreuses et dissémination métastatique, Med Sci (Paris), vol.32, pp.725-756, 2016.

R. Schofield, The relationship between the spleen colony-forming cell and the haemopoietic stem cell, Blood Cells, vol.4, pp.7-25, 1978.

D. T. Scadden, Nice neighborhood: Emerging concepts of the stem cell niche, Cell, vol.157, pp.41-50, 2014.

M. Jagut and J. Huynh, Régulation des cellules souches de la lignée germinale, Med Sci (Paris), vol.23, pp.611-619, 2007.
DOI : 10.1051/medsci/20072367611

URL : http://www.medecinesciences.org/articles/medsci/pdf/2007/08/medsci2007236-7p611.pdf

V. Barroca, B. Lassalle, and I. Allemand, Des progéniteurs transplantés peuvent générer des cellules souches germinales, Med Sci (Paris), vol.25, pp.893-898, 2009.
DOI : 10.1051/medsci/20092511893

URL : http://www.medecinesciences.org/articles/medsci/pdf/2009/11/medsci20092511p893.pdf

C. E. Adler, S. Alvarado, and A. , Types or states? Cellular dynamics and regenerative potential, Trends Cell Biol, vol.25, pp.687-96, 2015.
DOI : 10.1016/j.tcb.2015.07.008

URL : http://europepmc.org/articles/pmc4628888?pdf=render

D. Zipori, À la recherche d'une définition moléculaire plus que descriptive pour les cellules souches, Med Sci (Paris), vol.27, pp.303-310, 2011.
DOI : 10.1051/medsci/2011273303

URL : http://www.medecinesciences.org/articles/medsci/pdf/2011/03/medsci2011273p303.pdf

H. M. Blau, T. R. Brazelton, and J. M. Weimann, The evolving concept of a stem cell: entity or function?, Cell, vol.105, pp.829-870, 2001.

H. Mikkers and J. Frisen, Deconstructing stemness, J Eur Mol Biol Organ, vol.24, pp.2715-2724, 2005.
DOI : 10.1038/sj.emboj.7600749

URL : http://emboj.embopress.org/content/24/15/2715.full.pdf

L. Laplane, Cancer stem cells: Philosophy and therapies, 2016.
URL : https://hal.archives-ouvertes.fr/halshs-01426178

P. B. Gupta, C. M. Fillmore, and G. Jiang, Stochastic state transitions give rise to phenotypic equilibrium in populations of cancer cells, Cell, vol.146, pp.633-677, 2011.

A. Kreso and J. E. Dick, Evolution of the cancer stem cell model, Cell Stem Cell, vol.14, pp.275-91, 2014.

T. Reya, S. J. Morrison, and M. F. Clarke, Stem cells, cancer, and cancer stem cells, Nature, vol.414, pp.105-116, 2001.

S. Häfner and L. Coulombel, L'oligarchie contestée des cellules souches cancéreuses, Med Sci (Paris), vol.25, pp.227-235, 2009.

D. Reynaud, E. Pietras, and K. Barry-holson, IL-6 controls leukemic multipotent progenitor cell fate and contributes to chronic myelogenous leukemia development, Cancer Cell, vol.20, pp.661-73, 2011.
DOI : 10.1016/j.ccr.2011.10.012

URL : https://doi.org/10.1016/j.ccr.2011.10.012

R. S. Welner, G. Amabile, and D. Bararia, Treatment of chronic myelogenous leukemia by blocking cytokine alterations found in normal stem and progenitor cells, Cancer Cell, vol.27, pp.671-81, 2015.

C. L. Chaffer, I. Brueckmann, and C. Scheel, Normal and neoplastic nonstem cells can spontaneously convert to a stem-like state, Proc Natl Acad Sci, vol.108, pp.7950-7955, 2011.
DOI : 10.1073/pnas.1102454108

URL : http://www.pnas.org/content/108/19/7950.full.pdf

L. Vermeulen, D. Sousa, E. Van-der-heijden, and M. , Wnt activity defines colon cancer stem cells and is regulated by the microenvironment, Nat Cell Biol, vol.12, pp.468-76, 2010.
DOI : 10.1038/ncb2048

C. Thirant, B. Bessette, and P. Varlet, Clinical relevance of tumor cells with stem-like properties in pediatric brain tumors, PLoS One, vol.6, p.16375, 2011.
URL : https://hal.archives-ouvertes.fr/inserm-00573847

M. Latil, D. Nassar, and B. Beck, Cell-type-specific chromatin states differentially prime squamous cell carcinoma tumor-initiating cells for epithelial to mesenchymal transition, Cell Stem Cell, vol.20, pp.191-204, 2017.
DOI : 10.1016/j.stem.2016.10.018

URL : http://europepmc.org/articles/pmc5939571?pdf=render

C. L. Chaffer, N. D. Marjanovic, and T. Lee, Poised chromatin at the ZEB1 promoter enables breast cancer cell plasticity and enhances tumorigenicity, Cell, vol.154, pp.61-74, 2013.
DOI : 10.1016/j.cell.2013.06.005

URL : https://doi.org/10.1016/j.cell.2013.06.005

R. J. Whitson and A. E. Oro, Soil primes the seed: Epigenetic landscape drives tumor behavior, Cell Stem Cell, vol.20, pp.149-50, 2017.
DOI : 10.1016/j.stem.2017.01.007

URL : http://europepmc.org/articles/pmc5800310?pdf=render

P. D. Emanuel, L. J. Bates, and R. P. Castleberry, Selective hypersensitivity to granulocyte-macrophage colony-stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors, Blood, vol.77, pp.925-934, 1991.

J. Staerk and S. N. Constantinescu, The JAK-STAT pathway and hematopoietic stem cells from the JAK2 V617F perspective, JAK-STAT, vol.1, pp.184-190, 2012.
DOI : 10.4161/jkst.22071

URL : http://europepmc.org/articles/pmc3670242?pdf=render

W. Vainchenker, S. N. Constantinescu, and I. Plo, Recent advances in understanding myelofibrosis and essential thrombocythemia, F1000Research, vol.5, p.700, 2016.
DOI : 10.12688/f1000research.8081.1

URL : https://f1000research.com/articles/5-700/v1/pdf

K. Cheeseman, G. Certad, and J. B. Weitzman, Parasites et cancer : existe-t-il un lien ?, Med Sci (Paris), vol.32, pp.867-73, 2016.
DOI : 10.1051/medsci/20163210020

B. J. Huntly, H. Shigematsu, and K. Deguchi, MOZ-TIF2, but not BCRABL, confers properties of leukemic stem cells to committed murine hematopoietic progenitors, Cancer Cell, vol.6, pp.587-96, 2004.
DOI : 10.1016/j.ccr.2004.10.015

URL : https://doi.org/10.1016/j.ccr.2004.10.015

A. Cozzio, E. Passegue, and P. M. Ayton, Similar MLL-associated leukemias arising from self-renewing stem cells and short-lived myeloid progenitors, Genes Dev, vol.17, pp.3029-3064, 2003.
DOI : 10.1101/gad.1143403

URL : http://genesdev.cshlp.org/content/17/24/3029.full.pdf

L. Arranz, A. Sánchez-aguilera, and D. Martín-pérez, Neuropathy of haematopoietic stem cell niche is essential for myeloproliferative neoplasms, Nature, vol.512, pp.78-81, 2014.

D. A. Landau, K. Clement, and M. J. Ziller, Locally disordered methylation forms the basis of intratumor methylome variation in chronic lymphocytic leukemia, Cancer Cell, vol.26, pp.813-838, 2014.

J. Merlevede, N. Droin, and T. Qin, Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents, Nat Commun, vol.7, p.10767, 2016.
DOI : 10.1038/ncomms10767

URL : http://www.nature.com/articles/ncomms10767.pdf

H. Sager, W. C. Davis, and D. A. Dobbelaere, Macrophage-parasite relationship in theileriosis. Reversible phenotypic and functional dedifferentiation of macrophages infected with Theileria annulata, J Leukoc Biol, vol.61, pp.459-68, 1997.

H. Sager, G. Bertoni, and T. W. Jungi, Differences between B cell and macrophage transformation by the bovine parasite, Theileria annulata: a clonal approach, J Immunol, vol.161, pp.335-376, 1998.