Endogenous Myc controls mammalian epidermal cell size, hyperproliferation, endoreplication and stem cell amplification
Abstract
The transcription factor Myc (c-Myc) plays an important role in cell growth and cell death, yet its physiological function remains unclear. Ectopic activation of Myc has been recently suggested to regulate cell mass, and Drosophila dmyc controls cellular growth and size independently of cell division. By contrast, it has been proposed that in mammals Myc controls cell division and cell number. To gain insights into this debate we have specifically knocked out Myc in epidermis. Myc epidermal knockout mice are viable and their keratinocytes continue to cycle, but they display severe skin defects. The skin is tight and fragile, tears off in areas of mechanical friction and displays impaired wound healing. Steady-state epidermis is thinner, with loss of the proliferative compartment and premature differentiation. Remarkably, keratinocyte cell size, growth and endoreplication are reduced, and stem cell amplification is compromised. The results provide new and direct evidence for a role for endogenous Myc in cellular growth that is required for hyperproliferative cycles and tissue homeostasis.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Prior findings show that overexpression of c-Myc leads to enhanced SG expansion, while conditional deletion of c-Myc results in decreased SG size, cell proliferation, and sebocyte differentiation.
“previously reported findings where overexpression of c-Myc led to enhanced SG expansion, while conditional deletion of c-Myc resulted in decreased SG size, cell proliferation, and sebocyte differentiation3, 29, 38, 39.”
From Blimp1+ cells generate functional mouse sebaceous gland organoids in vitro (2019) · cites this paper as [38]
Cites
Defining the Epithelial Stem Cell Niche in Skin
Tumbar, T., Guasch, G., Greco, V., Blanpain, C., Lowry, W. E., Rendl, M., & Fuchs, E. (2004) · Science · doi:10.1126/science.1092436 · Cited by 2,031 · see citing works
Blanpain, C., Lowry, W. E., Geoghegan, A., Polak, L., & Fuchs, E. (2004) · Cell · doi:10.1016/j.cell.2004.08.012 · Cited by 1,428 · see citing works
The Myc/Max/Mad Network and the Transcriptional Control of Cell Behavior
Grandori, C., Cowley, S. M., James, L. P., & Eisenman, R. N. (2000) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.16.1.653 · Cited by 1,333 · see citing works
Three clonal types of keratinocyte with different capacities for multiplication.
Barrandon, Y., & Green, H. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.8.2302 · Cited by 1,293 · see citing works
Capturing and profiling adult hair follicle stem cells
Morris, R. J., Liu, Y., Marles, L., Yang, Z., Trempus, C., Li, S., Lin, J. S., Sawicki, J. A., & Cotsarelis, G. (2004) · Nature Biotechnology · doi:10.1038/nbt950 · Cited by 1,283 · see citing works
Jones, P. H., & Watt, F. M. (1993) · Cell · doi:10.1016/0092-8674(93)90251-k · Cited by 1,100 · see citing works
Integrin-Mediated Activation of Cdc42 Controls Cell Polarity in Migrating Astrocytes through PKCζ
Etienne‐Manneville, S., & Hall, A. K. (2001) · Cell · doi:10.1016/s0092-8674(01)00471-8 · Cited by 1,025 · see citing works
Edgar, B. A., & Orr‐Weaver, T. L. (2001) · Cell · doi:10.1016/s0092-8674(01)00334-8 · Cited by 843 · see citing works
c-Myc controls the balance between hematopoietic stem cell self-renewal and differentiation
Wilson, A., Murphy, M. J., Oskarsson, T., Kaloulis, K., Bettess, M. D., Oser, G. M., Pasche, A.-C., Knabenhans, C., MacDonald, H. R., & Trumpp, A. (2004) · Genes & Development · doi:10.1101/gad.313104 · Cited by 823 · see citing works
Drosophila myc Regulates Cellular Growth during Development
Johnston, L. A., Prober, D. A., Edgar, B. A., Eisenman, R. N., & Gallant, P. (1999) · Cell · doi:10.1016/s0092-8674(00)81512-3 · Cited by 648 · see citing works
Drosophila Myc Regulates Organ Size by Inducing Cell Competition
de la Cova, C., Abril, M., Bellosta, P., Gallant, P., & Johnston, L. A. (2004) · Cell · doi:10.1016/s0092-8674(04)00214-4 · Cited by 610 · see citing works
dMyc Transforms Cells into Super-Competitors
Moreno, E., & Basler, K. (2004) · Cell · doi:10.1016/s0092-8674(04)00262-4 · Cited by 597 · see citing works
Davis, A. C., Wims, M., Spotts, G. D., Hann, S., & Bradley, A. (1993) · Genes & Development · doi:10.1101/gad.7.4.671 · Cited by 531 · see citing works
Direct activation of RNA polymerase III transcription by c-Myc
Gomez-Roman, N., Grandori, C., Eisenman, R. N., & White, R. J. (2003) · Nature · doi:10.1038/nature01327 · Cited by 434 · see citing works
c-Myc regulates mammalian body size by controlling cell number but not cell size
Trumpp, A., Refaeli, Y., Óskarsson, T., Gasser, S., Murphy, M., Martin, G. R., & Bishop, J. M. (2001) · Nature · doi:10.1038/414768a · Cited by 434 · see citing works
Braun, K. M., Niemann, C., Jensen, U. B., Sundberg, J. P., Silva-Vargas, V., & Watt, F. M. (2003) · Development · doi:10.1242/dev.00703 · Cited by 425 · see citing works
Analysis of C-MYC Function in Normal Cells via Conditional Gene-Targeted Mutation
de Alborán, I. M., O’Hagan, R. C., Gärtner, F., Malynn, B. A., Davidson, L., Rickert, R. C., Rajewsky, K., DePinho, R. A., & Alt, F. W. (2001) · Immunity · doi:10.1016/s1074-7613(01)00088-7 · Cited by 398 · see citing works
Involucrin synthesis and tissue assembly by keratinocytes in natural and cultured human epithelia.
Banks-Schlegel, S. P., & Green, H. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.90.3.732 · Cited by 349 · see citing works
Plant cell-size control: growing by ploidy?
Kondorosi, É., Roudier, F., & Gendreau, E. (2000) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00118-7 · Cited by 348 · see citing works
Arnold, I., & Watt, F. M. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00154-3 · Cited by 341 · see citing works
N-myc can functionally replace c-myc in murine development, cellular growth, and differentiationPreprint
Malynn, B. A., de Alborán, I. M., O’Hagan, R. C., Bronson, R. T., Davidson, L., DePinho, R. A., & Alt, F. W. (2000) · Genes & Development · doi:10.1101/gad.14.11.1390 · Cited by 331 · see citing works
c-Myc promotes differentiation of human epidermal stem cells
Gandarillas, A., & Watt, F. M. (1997) · Genes & Development · doi:10.1101/gad.11.21.2869 · Cited by 326 · see citing works
Self-citationDeregulated expression of c-Myc depletes epidermal stem cells
Waikel, R. L., Kawachi, Y., Waikel, P. A., Wang, X.-J., & Roop, D. R. (2001) · Nature Genetics · doi:10.1038/88889 · Cited by 318 · see citing works
Activation of EGFP expression by Cre-mediated excision in a new ROSA26 reporter mouse strain
Mao, X., Fujiwara, Y., Chapdelaine-Williams, A. M., Yang, H., & Orkin, S. H. (2001) · Blood · doi:10.1182/blood.v97.1.324 · Cited by 291 · see citing works
Terminal differentiation of epidermal keratinocytes
Watt, F. M. (1989) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(89)80058-4 · Cited by 281 · see citing works
Sellheyer, K., Bickenbach, J. R., Rothnagel, J. A., Bundman, D. S., Longley, M. A., Krieg, T. M., Roche, N. S., Roberts, A. B., & Roop, D. R. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.11.5237 · Cited by 254 · see citing works
Ramı́rez, Á., Bravo, A., Jorcano, J. L., & Vidal, M. (1994) · Differentiation · doi:10.1046/j.1432-0436.1994.5810053.x · Cited by 206 · see citing works
p63 and the epithelial stem cell: more than status quo?Preprint
McKeon, F. (2004) · Genes & Development · doi:10.1101/gad.1190504 · Cited by 197 · see citing works
Ramı́rez, Á., Page, A., Gandarillas, A., Zanet, J., Pibre, S., Vidal, M., Tusell, L., Genescà, A., Whitaker, D. A., Melton, D. W., et al. (2004) · genesis · doi:10.1002/gene.20025 · Cited by 190 · see citing works
Self-citationEndoreduplication and development: rule without dividing?
Traas, J. A., Hülskamp, M., Gendreau, E., & Höfte, H. (1998) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(98)80042-3 · Cited by 190 · see citing works
Frye, M., Gardner, C., Li, E. R., Arnold, I., & Watt, F. M. (2003) · Development · doi:10.1242/dev.00462 · Cited by 187 · see citing works
Kim, S., Li, Q., Dang, C. V., & Lee, L. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.200372597 · Cited by 187 · see citing works
Myc and Max Homologs in Drosophila
Gallant, P., Shiio, Y., Cheng, P. F., Parkhurst, S. M., & Eisenman, R. N. (1996) · Science · doi:10.1126/science.274.5292.1523 · Cited by 176 · see citing works
dMyc is required for larval growth and endoreplication in Drosophila
Pierce, S. B., Yost, C., Britton, J. S., Loo, L. W. M., Flynn, E. M., Edgar, B. A., & Eisenman, R. N. (2004) · Development · doi:10.1242/dev.01108 · Cited by 163 · see citing works
Developmental Context Determines Latency of MYC-Induced Tumorigenesis
Beer, S., Zetterberg, A., Ihrie, R. A., McTaggart, R., Yang, Q., Bradon, N., Arvanitis, C., Attardi, L. D., Feng, S., Ruebner, B. H., et al. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020332 · Cited by 142 · see citing works
C-myc overexpression and p53 loss cooperate to promote genomic instability
Yin, X.-Y., Grove, L. E., Datta, N. S., Long, M. W., & Prochownik, E. V. (1999) · Oncogene · doi:10.1038/sj.onc.1202410 · Cited by 136 · see citing works
Levens, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.102173199 · Cited by 120 · see citing works
Drosophila dMyc is required for ovary cell growth and endoreplication
Maines, J. Z., Stevens, L. M., Tong, X., & Stein, D. (2004) · Development · doi:10.1242/dev.00932 · Cited by 110 · see citing works
c-Myc regulates cell size and ploidy but is not essential for postnatal proliferation in liver
Baena, E., Gandarillas, A., Vallespinós, M., Zanet, J., Bachs, O., Redondo, C., Fabregat, I., Martinez-A., C., & de Alborán, I. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409260102 · Cited by 104 · see citing works
Self-citationDrosophila Myc is oncogenic in mammalian cells and plays a role in the diminutive phenotype
Schreiber‐Agus, N., Stein, D., Chen, K., Goltz, J. S., Stevens, L. M., & DePinho, R. A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1235 · Cited by 99 · see citing works
Label-retaining keratinocytes and Langerhans cells in mouse epithelia
Mackenzie, I. C., & Bickenbach, J. R. (1985) · Cell and Tissue Research · doi:10.1007/bf00225420 · Cited by 97 · see citing works
Gandarillas, A., Davies, D. C., & Blanchard, J. (2000) · Oncogene · doi:10.1038/sj.onc.1203630 · Cited by 79 · see citing works
Self-citationMorgenbesser, S. D., Schreiber‐Agus, N., Bidder, M., Mahon, K. A., Overbeek, P. A., Horner, J., & DePinho, R. A. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb07053.x · Cited by 56 · see citing works
Romero, M. R., Caroll, J. M., & Watt, F. M. (1999) · Experimental Dermatology · doi:10.1111/j.1600-0625.1999.tb00348.x · Cited by 55 · see citing works
Lowry, R. B., Machin, G. A., Morgan, K., Mayock, D. E., Marx, L., Opitz, J. M., & Reynolds, J. F. (1985) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320220311 · Cited by 51 · see citing works
B-Myc Inhibits Neoplastic Transformation and Transcriptional Activation by c-Myc
Resar, L. M. S., Dolde, C. E., Barrett, J. F., & Dang, C. V. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.2.1130 · Cited by 47 · see citing works
Landay, M. F., Oster, S. K., Khosravi, F., Grove, L. E., Yin, X., Sedivy, J. M., Penn, L. Z., & Prochownik, E. V. (2000) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400701 · Cited by 36 · see citing works
Historical note on restrictive dermopathy and report of two new cases
Lenz, W., & Meschede, D. (1993) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320470824 · Cited by 12 · see citing works
Berlin, J. M., & Queen, J. R. (2002) · Archives of Dermatology · doi:10.1001/archderm.138.6.831 · Cited by 3 · see citing works
Tight Skin and Dysmorphic Features in a Newborn
Abrahamson, T. G., & Stone, M. S. (2002) · Archives of Dermatology · doi:10.1001/archderm.138.6.831-c · Cited by 1 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Scratching the surface of skin development
Fuchs, E. (2007) · Nature · doi:10.1038/nature05659 · Cited by 930 · see citing works
Epidermal Stem Cells of the Skin
Blanpain, C., & Fuchs, E. V. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104357 · Cited by 845 · see citing works
MYC, Metabolism, Cell Growth, and TumorigenesisPreprint
Dang, C. V. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014217 · Cited by 600 · see citing works
Blimp1 Defines a Progenitor Population that Governs Cellular Input to the Sebaceous Gland
Horsley, V., O'Carroll, D., Tooze, R., Ohinata, Y., Saitou, M., Obukhanych, T., Nussenzweig, M., Tarakhovsky, A., & Fuchs, E. (2006) · Cell · doi:10.1016/j.cell.2006.06.048 · Cited by 426 · see citing works
Jensen, K. B., & Watt, F. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601886103 · Cited by 321 · see citing works
Lactate dehydrogenase activity drives hair follicle stem cell activation
Flores, A., Schell, J., Krall, A. S., Jelinek, D., Miranda, M., Grigorian, M., Braas, D., White, A. C., Zhou, J. L., Graham, N. A., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3575 · Cited by 301 · see citing works
Hair Follicle Stem Cells Provide a Functional Niche for Melanocyte Stem Cells
谷村, 心., Tadokoro, Y., Inomata, K., Bình, N. T., Nishie, W., Yamazaki, S., Nakauchi, H., Tanaka, Y., McMillan, J. R., Sawamura, D., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2010.11.029 · Cited by 300 · see citing works
Rapid Loss of Intestinal Crypts upon Conditional Deletion of the Wnt/Tcf-4 Target Gene c-Myc
Muncan, V., Sansom, O. J., Tertoolen, L. G. J., Phesse, T. J., Begthel, H., Sancho, E., Cole, A. M., Gregorieff, A., de Alborán, I. M., Clevers, H. C., et al. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00821-06 · Cited by 249 · see citing works
More than one way to skin . . .
Fuchs, E., & Horsley, V. (2008) · Genes & Development · doi:10.1101/gad.1645908 · Cited by 224 · see citing works
Epidermal stem cells: an update
Watt, F. M., Celso, C. L., & Silva-Vargas, V. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.08.006 · Cited by 193 · see citing works
Transcriptional Control of Wound Repair
Schäfer, M., & Werner, S. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123609 · Cited by 187 · see citing works
Sebocytes, multifaceted epithelial cells: Lipid production and holocrine secretion
Schneider, M. R., & Paus, R. (2010) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.11.017 · Cited by 199 · see citing works
Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle
Geyfman, M., Plikus, M. V., Treffeisen, E. R., D, B. A. M., & Paus, R. (2014) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12151 · Cited by 173 · see citing works
Shaw, T., & Martin, P. (2009) · The EMBO Reports · doi:10.1038/embor.2009.102 · Cited by 171 · see citing works
Cell growth dilutes the cell cycle inhibitor Rb to trigger cell division
Zatulovskiy, E. A., Zhang, S., Berenson, D. F., Topacio, B. R., & Skotheim, J. M. (2020) · Science · doi:10.1126/science.aaz6213 · Cited by 164 · see citing works
MYC in mammalian epidermis: how can an oncogene stimulate differentiation?
Watt, F. M., Frye, M., & Benitah, S. A. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2328 · Cited by 157 · see citing works
Role of Src family kinases and N-Myc in spermatogonial stem cell proliferation
Braydich‐Stolle, L. K., Kostereva, N. V., Dym, M., & Hofmann, M.-C. C. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.12.013 · Cited by 149 · see citing works
The MAX-interacting transcription factor network
Hurlin, P. J., & Huang, J. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.07.009 · Cited by 147 · see citing works
Blocking Myc to Treat Cancer: Reflecting on Two Decades of Omomyc
Massó-Vallés, D., & Soucek, L. (2020) · Cells · doi:10.3390/cells9040883 · Cited by 141 · see citing works
Notch cooperates with Lozenge/Runx to lock haemocytes into a differentiation programme
Terriente-Félix, A., Li, J., Collins, S., Mulligan, A., Reekie, I. R., Bernard, F., Krejčı́, A., & Bray, S. J. (2013) · Development · doi:10.1242/dev.086785 · Cited by 120 · see citing works
Cancer stem cells and cell size: A causal link?
Li, Q., Rycaj, K., Chen, X., & Tang, D. G. (2015) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2015.07.002 · Cited by 119 · see citing works
The Role of MIZ-1 in MYC-Dependent TumorigenesisPreprint
Wiese, K. E., Walz, S., von Eyß, B., Wolf, E., Athineos, D., Sansom, O. J., & Eilers, M. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014290 · Cited by 111 · see citing works
Zanet, J., Freije, A., Ruiz‐Soto, M., Coulon, V., Sanz, J. R., Chiésa, J., & Gandarillas, A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015701 · Cited by 111 · see citing works
Self-citationShh Controls Epithelial Proliferation via Independent Pathways that Converge on N-Myc
Mill, P., Mo, R., Hu, M., Dagnino, L., Rosenblum, N. D., & Hui, C. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.05.009 · Cited by 107 · see citing works
Myc's other life: stem cells and beyond
Laurenti, E., Wilson, A., & Trumpp, A. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.09.006 · Cited by 101 · see citing works
miR-24 triggers epidermal differentiation by controlling actin adhesion and cell migration
Amelio, I., Lena, A. M., Viticchiè, G., Shalom‐Feuerstein, R., Terrinoni, A., Dinsdale, D. D., Russo, G., Fortunato, C., Bonanno, E., Spagnoli, L. G., et al. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201203134 · Cited by 88 · see citing works
Hooker, C. W., & Hurlin, P. J. (2006) · Journal of Cell Science · doi:10.1242/jcs.02815 · Cited by 81 · see citing works
Óskarsson, T., Essers, M. A. G., Dubois, N. C., Offner, S. E., Dubey, C., Roger, C., METZGER, D., Chambon, P., Hümmler, E., Beard, P., et al. (2006) · Genes & Development · doi:10.1101/gad.381206 · Cited by 82 · see citing works
MYC and KRAS cooperation: from historical challenges to therapeutic opportunities in cancer
Casacuberta‐Serra, S., González-Larreategui, Í., Capitán-Leo, D., & Soucek, L. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01907-z · Cited by 80 · see citing works
2,3,7,8-Tetrachlorodibenzo-p-dioxin alters sebaceous gland cell differentiation in vitro
Ju, Q., Fimmel, S., Hinz, N., Stahlmann, R., Xia, L., & Zouboulis, C. C. (2011) · Experimental Dermatology · doi:10.1111/j.1600-0625.2010.01204.x · Cited by 74 · see citing works
N6‐methyladenosine modification of lncRNA Pvt1 governs epidermal stemness
Lee, J., Wu, Y., Harada, B. T., Li, Y., Zhao, J. C., He, C., Ma, Y., & Wu, X. (2021) · The EMBO Journal · doi:10.15252/embj.2020106276 · Cited by 70 · see citing works
Cellular and Molecular Progression of Prostate Cancer: Models for Basic and Preclinical Research
Saranyutanon, S., Deshmukh, S. K., Dasgupta, S., Pai, S. G., Singh, S., & Singh, A. P. (2020) · Cancers · doi:10.3390/cancers12092651 · Cited by 65 · see citing works
Targeting MYC Proteins for Tumor Therapy
Wolf, E., & Eilers, M. (2019) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030518-055826 · Cited by 63 · see citing works
Freije, A., Molinuevo, R., Ceballos, L., Cagigas, M., Alonso‐Lecue, P., Rodrı́guez, R., Menéndez, P. R., Aberdam, D., de Diego, E., & Gandarillas, A. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.012 · Cited by 62 · see citing works
Self-citationThe mysterious human epidermal cell cycle, or an oncogene-induced differentiation checkpoint
Gandarillas, A. (2012) · Cell Cycle · doi:10.4161/cc.22529 · Cited by 61 · see citing works
Self-citationUniversal encoding of pan-cancer histology by deep texture representations
Komura, D., Kawabe, A., Fukuta, K., Sano, K., Umezaki, T., Koda, H., Suzuki, R. H., Tominaga, K., Ochi, M., Konishi, H., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110424 · Cited by 62 · see citing works
Acosta, J. C., Ferrándiz, N., Bretones, G., Torrano, V., Blanco, R. E., Richard, C., O’Connell, B. C., Sedivy, J. M., Delgado, M. D., & León, J. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00752-08 · Cited by 58 · see citing works
Duperret, E. K., Dahal, A., & Ridky, T. W. (2015) · Journal of Cell Science · doi:10.1242/jcs.175539 · Cited by 58 · see citing works
Myc is required for β-catenin-mediated mammary stem cell amplification and tumorigenesis
Moumen, M., Chiche, A., Decraene, C., Petit, V., Gandarillas, A., Deugnier, M., Glukhova, M. A., & Faraldo, M. M. (2013) · Molecular Cancer · doi:10.1186/1476-4598-12-132 · Cited by 55 · see citing works
Self-citationRole of c-Myc in intestinal tumorigenesis of the Apc min/+ mouse1
Ignatenko, N. A., Holubec, H., Besselsen, D. G., Blohm-Mangone, K. A., Padilla‐Torres, J., Nagle, R. B., de Alborán, I. M., Guillen-Rodriguez, J., & Gerner, E. W. (2006) · Cancer Biology & Therapy · doi:10.4161/cbt.5.12.3376 · Cited by 54 · see citing works
Unveiling Hair Follicle Stem Cells
Yang, L., & Peng, R. (2010) · Stem Cell Reviews and Reports · doi:10.1007/s12015-010-9172-z · Cited by 54 · see citing works
Blimp1+ cells generate functional mouse sebaceous gland organoids in vitro
Feldman, A., Mukha, D., Maor, I. I., Sedov, E., Koren, E., Yosefzon, Y., Shlomi, T., & Fuchs, Y. (2019) · Nature Communications · doi:10.1038/s41467-019-10261-6 · Cited by 52 · see citing works
N-myc functions in transcription and development
Hurlin, P. J. (2005) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20059 · Cited by 51 · see citing works
Neuregulin3 alters cell fate in the epidermis and mammary gland
Panchal, H., Wansbury, O., Parry, S., Ashworth, A., & Howard, B. A. (2007) · BMC Developmental Biology · doi:10.1186/1471-213x-7-105 · Cited by 48 · see citing works
C‐myc as a modulator of renal stem/progenitor cell population
Couillard, M., & Trudel, M. (2009) · Developmental Dynamics · doi:10.1002/dvdy.21841 · Cited by 49 · see citing works
Grendler, J., Lowgren, S., Mills, M. T., & Losick, V. P. (2018) · Development · doi:10.1242/dev.173005 · Cited by 40 · see citing works
Cyclin E drives human keratinocyte growth into differentiation
Freije, A., Ceballos, L., Coisy‐Quivy, M., Barnes, L., Rosa‐Garrido, M., de Diego, E., Blanchard, J., & Gandarillas, A. (2012) · Oncogene · doi:10.1038/onc.2012.22 · Cited by 47 · see citing works
Self-citationDisruption of Smad4 in Mouse Epidermis Leads to Depletion of Follicle Stem Cells
Yang, L., Wang, L., & Yang, X. Y. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-07-0731 · Cited by 47 · see citing works
Control of Vertebrate Development by MYCPreprint
Hurlin, P. J. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014332 · Cited by 47 · see citing works
Acidic fibroblast growth factor underlies microenvironmental regulation of MYC in pancreatic cancer
Bhattacharyya, S., Oon, C. H., Kothari, A., Horton, W. R., Link, J. M., Sears, R. C., & Sherman, M. H. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20191805 · Cited by 44 · see citing works
Myc in model organisms: A view from the flyroom
de la Cova, C., & Johnston, L. A. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.07.010 · Cited by 44 · see citing works
Conditional Deletion ofc-mycDoes Not Impair Liver Regeneration
Li, F., Xiang, Y., Potter, J. J., Dinavahi, R., Dang, C. V., & Lee, L. A. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-4242 · Cited by 44 · see citing works
Epidermal Receptor Activator of NF-κB Ligand Controls Langerhans Cells Numbers and Proliferation,
Barbaroux, J.-B., Beleut, M., Brisken, C., Mueller, C. G., & Groves, R. W. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.2.1103 · Cited by 43 · see citing works
The Proto-Oncogene Myc Is Essential for Mammary Stem Cell Function
Moumen, M., Chiche, A., Deugnier, M., Petit, V., Gandarillas, A., Glukhova, M. A., & Faraldo, M. M. (2012) · Stem Cells · doi:10.1002/stem.1090 · Cited by 42 · see citing works
Self-citationEffects and mechanisms of polycyclic aromatic hydrocarbons in inflammatory skin diseases
Jin, H., Lin, Z., Pang, T., Wu, J., Zhao, C., Zhang, Y., Lei, Y., Li, Q., Yao, X., Zhao, M., et al. (2024) · Science of The Total Environment · doi:10.1016/j.scitotenv.2024.171492 · Cited by 41 · see citing works
Hierarchy of cellular decisions in collective behavior: Implications for wound healing
Wickert, L. E., Pomerenke, S., Mitchell, I., Masters, K. S. B., & Kreeger, P. K. (2016) · Scientific Reports · doi:10.1038/srep20139 · Cited by 38 · see citing works
Sanders, J. A., Schorl, C., Patel, A. J., Sedivy, J. M., & Gruppuso, P. A. (2012) · BMC Physiology · doi:10.1186/1472-6793-12-1 · Cited by 38 · see citing works
c-Myc affects mRNA translation, cell proliferation and progenitor cell function in the mammary gland
Stoelzle, T., Schwarb, P., Trumpp, A., & Hynes, N. E. (2009) · BMC Biology · doi:10.1186/1741-7007-7-63 · Cited by 38 · see citing works
Transcriptional regulation of wound inflammation
Haertel, E., Werner, S., & Schäfer, M. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2014.01.005 · Cited by 37 · see citing works
Basyuk, E. I., Coulon, V., Digarcher, A. L., Coisy‐Quivy, M., Molès, J., Gandarillas, A., & Journot, L. (2005) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-05-0019 · Cited by 37 · see citing works
Self-citationTranscriptional control of skin reepithelialization
Bellavia, G., Fasanaro, P., Melchionna, R., Capogrossi, M. C., & Napolitano, M. (2013) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2013.08.007 · Cited by 37 · see citing works
Myc Prevents Apoptosis and Enhances Endoreduplication Induced by Paclitaxel
Gatti, G., Maresca, G., Natoli, M., Florenzano, F., Nicolin, A., Felsani, A., & D’Agnano, I. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005442 · Cited by 36 · see citing works
CIP2A increases self-renewal and is linked to Myc in neural progenitor cells
Kerosuo, L., Fox, H., Perälä, N., Ahlqvist, K., Suomalainen, A., Westermarck, J., Sariola, H., & Wartiovaara, K. (2010) · Differentiation · doi:10.1016/j.diff.2010.04.003 · Cited by 35 · see citing works
Nieuwenhuis, E., Barnfield, P. C., Makino, S., & Hui, C. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.06.016 · Cited by 35 · see citing works
Magnetic separation and characterization of keratinocyte stem cells from human gingiva
Calenic, B., Ishkitiev, N., Yaegaki, K., Imai, T., Kumazawa, Y., Nasu, M., & Hirata, T. M. (2010) · Journal of Periodontal Research · doi:10.1111/j.1600-0765.2010.01284.x · Cited by 34 · see citing works
Genetically modified laboratory mice with sebaceous glands abnormalities
Ehrmann, C., & Schneider, M. R. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2312-0 · Cited by 33 · see citing works
B lymphocyte-induced maturation protein 1 is a novel target gene of aryl hydrocarbon receptor
Ikuta, T., Ohba, M., Zouboulis, C. C., Fujii‐Kuriyama, Y., & Kawajiri, K. (2010) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2010.04.003 · Cited by 31 · see citing works
Growth-promoting and tumourigenic activity of c-Myc is suppressed by Hhex
Marfil, V., Blazquez, M., Serrano, F., Castell, J. V., & Bort, R. (2014) · Oncogene · doi:10.1038/onc.2014.240 · Cited by 30 · see citing works
Transient cardiomyocyte fusion regulates cardiac development in zebrafish
Sawamiphak, S., Kontarakis, Z., Filosa, A., Reischauer, S., & Stainier, D. Y. R. (2017) · Nature Communications · doi:10.1038/s41467-017-01555-8 · Cited by 28 · see citing works
Ojeh, N. O., Pekovic‐Vaughan, V., Jahoda, C. A. B., & Määttå, A. (2008) · Journal of Cell Science · doi:10.1242/jcs.025643 · Cited by 27 · see citing works
Aho, S., Lupo, J., Coly, P., Sabine, A., Castellazzi, M., Morand, P., Sergeant, A., Manet, É., Boyer, V., & Gruffat, H. (2008) · Biology of the Cell · doi:10.1042/bc20080072 · Cited by 27 · see citing works
Liu, D., He, M. L., Yi, B., Guo, W.-H., Que, A.-L., & Zhang, J. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.05.021 · Cited by 27 · see citing works
Neumann, C., Bigliardi‐Qi, M., Widmann, C., & Bigliardi, P. L. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.370 · Cited by 26 · see citing works
Wang, Z., Zhang, G., Le, Y., Ju, J., Zhang, P., Wan, D., Zhao, Q., Jin, G., Su, H., Liu, J., et al. (2020) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmaa091 · Cited by 26 · see citing works
Wan, D., Fu, Y., Le, Y., Zhang, P., Ju, J., Wang, B., Zhang, G., Wang, Z., Su, H., Wang, L., et al. (2019) · Stem Cells International · doi:10.1155/2019/1575480 · Cited by 25 · see citing works
Kawamura, K., Tachibana, M., & Sunanaga, T. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21592 · Cited by 25 · see citing works
Bernabé‐Rubio, M., Ali, S., Bhosale, P. G., Goss, G., Mobasseri, S. A., Tapia‐Rojo, R., Zhu, T., Hiratsuka, T., Battilocchi, M., Tomás, I. M., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01234-5 · Cited by 24 · see citing works
Irs2 Inactivation Suppresses Tumor Progression in Pten+/− Mice
Szabolcs, M. J., Keniry, M. E., Simpson, L., Reid, L. J., Koujak, S., Schiff, S. C., Davidian, G., Licata, S. E., Gruvberger-Saal, S. K., Murty, V. V. V. S., et al. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080086 · Cited by 24 · see citing works
Cutaneous stem cells: something new and something borrowed
Sun, X., Fu, X., & Sheng, Z. (2007) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2007.00282.x · Cited by 21 · see citing works
Muñoz-Alonso, M. J., Ceballos, L., Bretones, G., Frade, P., León, J., & Gandarillas, A. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.22935 · Cited by 20 · see citing works
Self-citationEnhancement of Cutaneous Wound Healing by Dsg2 Augmentation of uPAR Secretion
Cooper, F., Overmiller, A. M., Loder, A., Brennan-Crispi, D. M., McGuinn, K. P., Marous, M. R., Freeman, T. A., Galdo, N. A. R., Siracusa, L. D., Wahl, J. K., et al. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.04.024 · Cited by 19 · see citing works
Epidermal stem cell fate: what can we learn from embryonic stem cells?
Aberdam, D. (2007) · Cell and Tissue Research · doi:10.1007/s00441-007-0497-0 · Cited by 18 · see citing works
Wang, X., Langer, E. M., Daniel, C. J., Janghorban, M., Wu, V. F., Wang, X., & Sears, R. C. (2020) · Oncogenesis · doi:10.1038/s41389-020-00261-3 · Cited by 18 · see citing works
Miz1 Is a Critical Repressor of cdkn1a during Skin Tumorigenesis
Hönnemann, J., Sanz‐Moreno, A., Wolf, E., Eilers, M., & Elsässer, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034885 · Cited by 17 · see citing works
In vitro differentiation of murine embryonic stem cells into keratinocyte-like cells
Haase, I., Knaup, R., Wartenberg, M., Sauer, H., Hescheler, J., & Mahrle, G. (2007) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2007.07.001 · Cited by 17 · see citing works
Choi, H., Jackson, N. L., Shaw, D. R., Emanuel, P. D., Liu, Y. L., Tousson, A., Meng, Z., & Blume, S. W. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21909 · Cited by 17 · see citing works
Myc in Stem Cell Behaviour: Insights from Drosophila
Quinn, L. M., Secombe, J., & Hime, G. R. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-6621-1_15 · Cited by 16 · see citing works
Chloracne: From clinic to research
Ju, Q., Yang, K., Zouboulis, C. C., Ring, J., & Chen, W. (2012) · Dermatologica Sinica · doi:10.1016/j.dsi.2012.01.007 · Cited by 16 · see citing works
Charruyer, A., Weisenberger, T., Li, H., Khalifa, A., Schroeder, A., Belzer, A., & Ghadially, R. (2021) · Aging Cell · doi:10.1111/acel.13310 · Cited by 16 · see citing works
Manipulating Myc for reparative regeneration
Ascanelli, C., Dahir, R., & Wilson, C. H. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1357589 · Cited by 14 · see citing works
Portal, C., Wang, Z., Scott, D. K., Wolosin, J. M., & Iomini, C. (2022) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.63.2.3 · Cited by 13 · see citing works
Meibomian gland development: Where, when and how?
Verma, S., Moreno, I. Y., Trapp, M. E., Ramirez, L., Gesteira, T. F., & Coulson‐Thomas, V. J. (2023) · Differentiation · doi:10.1016/j.diff.2023.04.005 · Cited by 13 · see citing works
O’Toole, E. A., & Mellerio, J. E. (2010) · doi:10.1002/9781444317633.ch14 · Cited by 13 · see citing works
Oh, the Mutations You’ll Acquire! A Systematic Overview of Cutaneous Squamous Cell Carcinoma
Droll, S. H., & Bao, X. (2021) · Cellular Physiology and Biochemistry · doi:10.33594/000000433 · Cited by 12 · see citing works
Shimoda, M., Lyu, Y., Wang, K.-H., Kumar, A., Miura, H., Meckler, J. F., Davis, R. R., Chantarasrivong, C., Izumiya, C., Tepper, C. G., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02853-0 · Cited by 11 · see citing works
Nikolova, E., Mitev, V., Minner, F., Deroanne, C., & Poumay, Y. (2007) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21455 · Cited by 11 · see citing works
Caragine, C. M., Le, V. T., Mustafa, M., Diaz, B. J., Morris, J. A., Müller, S., Méndez‐Mancilla, A., Geller, E. T., Liscovitch‐Brauer, N., & Sanjana, N. E. (2025) · Nature Communications · doi:10.1038/s41467-025-56568-5 · Cited by 9 · see citing works
Yanku, Y., Bitman-Lotan, E., Zohar, Y., Kurant, E., Zilke, N., Eilers, M., & Orian, A. (2018) · Cells · doi:10.3390/cells7100151 · Cited by 9 · see citing works
Role of mTOR Signaling Cascade in Epidermal Morphogenesis and Skin Barrier Formation
Wang, J., Eming, S. A., & Ding, X. (2022) · Biology · doi:10.3390/biology11060931 · Cited by 8 · see citing works
c-Myc and Activated Ras During Skin Tumorigenesis: Cooperation at the Cancer Stem Cell Level?
Trumpp, A. (2007) · Springer eBooks · doi:10.1007/2789_2007_042 · Cited by 7 · see citing works
- Authors
- Zanet, J., Pibre, S., Jacquet, C., Ramirez, A., de Alborán, I. M., & Gandarillas, A.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Epithelial Damage, Repair and Tissue Engineering Program, CIEMAT, Madrid, Spain
- Centro Nacional de Biotecnologia, CSIC, Madrid, Spain
- Corresponding author
- Gandarillas, Alberto
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2005-04-15
- Volume
- 118
- Issue
- 8
- Pages
- 1693-1704
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W2101568666
- Cited by
- 123
- References
- 50
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 6 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 7 · 2019: 6 · 2018: 2 · 2017: 2 · 2016: 3 · 2015: 3 · 2014: 6 · 2013: 8 · 2012: 8
- FWCI
- 12.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cell Science (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- HighWire Press Open Archive (submittedVersion)
- Topics
- Health Sciences › Medicine › Urology › Hair Growth and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- c-Myc, epidermis, keratinocytes, cell size, cell growth, endoreplication, hyperproliferation, epidermal stem cells, wound healing, skin defects, tissue homeostasis, cell differentiation
- MeSH terms
- Animals, Cell Cycle, Cell Differentiation, Cell Division, Cell Movement, Epidermis, Female, Homeostasis, Male, Mice, Transgenic, Ploidies, Stem Cells, Stress, Mechanical, Wound Healing, Keratinocytes, Proto-Oncogene Proteins c-myc, Mice, Knockout, Hair Follicle, Cell Size, Cell Enlargement, Cell Proliferation, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review