The DOI matches its Crossref record; 31 of the 32 references it cites were found in a registry or an index.
Cyclins D2 and D1 Are Essential for Postnatal Pancreatic β-Cell Growth
Open accessAbstract
Regulation of adult beta-cell mass in pancreatic islets is essential to preserve sufficient insulin secretion in order to appropriately regulate glucose homeostasis. In many tissues mitogens influence development by stimulating D-type cyclins (D1, D2, or D3) and activating cyclin-dependent kinases (CDK4 or CDK6), which results in progression through the G(1) phase of the cell cycle. Here we show that cyclins D2 and D1 are essential for normal postnatal islet growth. In adult murine islets basal cyclin D2 mRNA expression was easily detected, while cyclin D1 was expressed at lower levels and cyclin D3 was nearly undetectable. Prenatal islet development occurred normally in cyclin D2(-/-) or cyclin D1(+/-) D2(-/-) mice. However, beta-cell proliferation, adult mass, and glucose tolerance were decreased in adult cyclin D2(-/-) mice, causing glucose intolerance that progressed to diabetes by 12 months of age. Although cyclin D1(+/-) mice never developed diabetes, life-threatening diabetes developed in 3-month-old cyclin D1(-/+) D2(-/-) mice as beta-cell mass decreased after birth. Thus, cyclins D2 and D1 were essential for beta-cell expansion in adult mice. Strategies to tightly regulate D-type cyclin activity in beta cells could prevent or cure diabetes.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“During physiological growth in humans, mice and other species, juvenile β-cells expand by self-renewal7,8 while maintaining their hallmark functions.”
From PDGF signalling controls age-dependent proliferation in pancreatic β-cells (2011) · cites this paper as [8]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
β-Cell Deficit and Increased β-Cell Apoptosis in Humans With Type 2 Diabetes
Butler, A. E., Janson, J., Bonner-Weir, S., Ritzel, R., Rizza, R. A., & Butler, P. C. (2003) · Diabetes · doi:10.2337/diabetes.52.1.102 · Cited by 4,011
Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation
Dor, Y., Brown, J., Martinez, O. I., & Melton, D. A. (2004) · Nature · doi:10.1038/nature02520 · Cited by 2,219
Disruption of IRS-2 causes type 2 diabetes in mice
Withers, D. J., Gutierrez, J. S., Towery, H. H., Burks, D. J., Ren, J., Previs, S. F., Zhang, Y., Bernal, D., Pons, S., Shulman, G. I., et al. (1998) · Nature · doi:10.1038/36116 · Cited by 1,775
Self-citationThe Pezcoller lecture: cancer cell cycles revisited.
Sherr, C. J. (2000) · PubMed · Cited by 1,193
Cyclin D1 provides a link between development and oncogenesis in the retina and breast
Sicinski, P., Donaher, J. L., Parker, S. B., Li, T., Fazeli, A., Gardner, H., Haslam, S. Z., Bronson, R. T., Elledge, S. J., & Weinberg, R. A. (1995) · Cell · doi:10.1016/0092-8674(95)90034-9 · Cited by 1,021
IRS proteins and the common path to diabetes
White, M. F. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00514.2001 · Cited by 925
Self-citationβ-Cell death during progression to diabetes
Mathis, D. J., Vence, L., & Benoist, C. O. (2001) · Nature · doi:10.1038/414792a · Cited by 884
Rane, S. G., Dubus, P., Mettus, R. V., Galbreath, E. J., Boden, G., Reddy, E. P., & Barbacid, M. (1999) · Nature Genetics · doi:10.1038/8751 · Cited by 700 · cited 3×
“By contrast, constitutively active cdk4 introduced into the mouse genome—by substitution of Arg-24 to Cys-24 that renders cdk4 insensitive to inhibition by p16—expanded the mass of physiologically functional cells (19, 21).”
BackgroundResultCyclin D2 is an FSH-responsive gene involved in gonadal cell proliferation and oncogenesis
Siciński, P., Donaher, J. L., Geng, Y., Parker, S. B., Gardner, H., Park, M. Y., Robker, R. L., Richards, J. S., McGinnis, L. K., Biggers, J. D., et al. (1996) · Nature · doi:10.1038/384470a0 · Cited by 697
Mice lacking cyclin D1 are small and show defects in eye and mammary gland development.
Fantl, V, Stamp, G., Andrews, A., Rosewell, I., & Dickson, C. (1995) · Genes & Development · doi:10.1101/gad.9.19.2364 · Cited by 691
Flagged first, then by citations
1 of the 32 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- 10.1172/JCI0214439 · DOI
- Sherr C. J, 2000, Cancer Res., 60, 3689
Cited by
Sorted by citations
Items 101–200 of 334
The prolactin receptor: Diverse and emerging roles in pathophysiology
Gorvin, C. M. (2015) · Journal of Clinical & Translational Endocrinology · doi:10.1016/j.jcte.2015.05.001 · Cited by 65
Salpeter, S. J., Klochendler, A., Weinberg-Corem, N., Porat, S., Granot, Z., Shapiro, A. M. J., Magnuson, M. A., Eden, A., Grimsby, J. S., Gläser, B., et al. (2011) · Endocrinology · doi:10.1210/en.2010-1372 · Cited by 64
Yang, Y., Chang, B. H., & Chan, L. (2012) · EMBO Molecular Medicine · doi:10.1002/emmm.201201398 · Cited by 65
Gleason, C. E., Ning, Y., Cominski, T. P., Gupta, R. K., Kaestner, K. H., Pintar, J. E., & Birnbaum, M. J. (2009) · Molecular Endocrinology · doi:10.1210/me.2009-0167 · Cited by 63
Expression profiling of cell cycle genes in human pancreatic islets with and without type 2 diabetes
Taneera, J., Fadista, J., Ahlqvist, E., Zhang, M., Wierup, N., Renström, E., & Groop, L. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.05.003 · Cited by 65
Dai, F. F., Zhang, Y., Kang, Y., Wang, Q., Gaisano, H. Y., Braunewell, K., Chan, C. B., & Wheeler, M. B. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512924200 · Cited by 65
Figeac, F., Uzan, B., Faro, M., Chelali, N., Portha, B., & Movassat, J. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00538.2009 · Cited by 63
Cell cycle control of β-cell replication in the prenatal and postnatal human pancreas
Köhler, C. U., Olewinski, M., Tannapfel, A., Schmidt, W. E., Fritsch, H., & Meier, J. J. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00496.2010 · Cited by 64
Jackerott, M., Møldrup, A., Thams, P., Galsgaard, E. D., Knudsen, J. G., Lee, Y. C., & Nielsen, J. H. (2006) · Diabetes · doi:10.2337/db06-0244 · Cited by 63
Ji, Y., Sun, S., Shrestha, N., Darragh, L. B., Shirakawa, J., Xing, Y., He, Y., Carboneau, L., Kim, H., An, D., et al. (2019) · Nature Immunology · doi:10.1038/s41590-019-0396-z · Cited by 64
Liganded Thyroid Hormone Receptor-α Enhances Proliferation of Pancreatic β-Cells
Furuya, F., Shimura, H., Yamashita, S., Endo, T., & Kobayashi, T. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.100222 · Cited by 62
Vagal control of pancreatic β-cell proliferation
Lausier, J., Diaz, W. C., Roskens, V. A., LaRock, K., Herzer, K., Fong, C. G., Latour, M. G., Peshavaria, M., & Jetton, T. L. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00202.2010 · Cited by 63
Emerging roles of GLIS3 in neonatal diabetes, type 1 and type 2 diabetes
Wen, X., & Yang, Y. (2016) · Journal of Molecular Endocrinology · doi:10.1530/jme-16-0232 · Cited by 62
Xu, T., Yang, L., Yan, C., Wang, X., Huang, P., Zhao, F., Zhao, L., Zhang, M., Jia, W., Wang, X., et al. (2014) · Cell Research · doi:10.1038/cr.2014.55 · Cited by 60
Exendin-4 induction of cyclin D1 expression in INS-1 β-cells: involvement of cAMP-responsive element
Kim, M., Kang, J.-H., Park, Y. G., Ryu, G. R., Ko, S., Jeong, I.-K., Koh, K.-H., Rhie, D.-J., Yoon, S., Hahn, S. J., et al. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06480 · Cited by 60
Chen, H., Kleinberger, J. W., Takane, K. K., Salim, F. G., Fiaschi‐Taesch, N., Pappas, K., Parsons, R. E., Jiang, J., Zhang, Y., Liu, H., et al. (2015) · Diabetes · doi:10.2337/db15-0083 · Cited by 59
ICA512 signaling enhances pancreatic β-cell proliferation by regulating cyclins D through STATs
Mziaut, H., Kersting, S., Knoch, K.-P., Fan, W.-H., Trajkovski, M., Erdmann, K., Bergert, H., Ehehalt, F., Saeger, H., & Solimena, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710931105 · Cited by 59
Cózar‐Castellano, I., Harb, G., Selk, K. L., Takane, K. K., Vasavada, R. C., Sicari, B. M., Law, B. K., Zhang, P., Scott, D. K., Fiaschi‐Taesch, N., et al. (2008) · Diabetes · doi:10.2337/db08-0393 · Cited by 59
Tavana, O., Puebla-Osorio, N., Sang, M., & Zhu, C. (2010) · Diabetes · doi:10.2337/db09-0792 · Cited by 58
Participation of Akt, Menin, and p21 in Pregnancy-Induced β-Cell Proliferation
Hughes, E., & Huang, C. (2011) · Endocrinology · doi:10.1210/en.2010-1250 · Cited by 56
Pancreatic beta-cells: From generation to regeneration
Collombat, P., Xu, X., Heimberg, H., & Mansouri, A. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.07.007 · Cited by 56
Δ40 Isoform of p53 Controls β-Cell Proliferation and Glucose Homeostasis in Mice
Hinault, C., Kawamori, D., Liew, C. W., Maier, B., Hu, J., Keller, S. R., Mirmira, R. G., Scrable, H. J., & Kulkarni, R. (2011) · Diabetes · doi:10.2337/db09-1379 · Cited by 57
Hayes, H. L., Moss, L. G., Schisler, J. C., Haldeman, J. M., Zhang, Z., Rosenberg, P. B., Newgard, C. B., & Hohmeier, H. E. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00469-13 · Cited by 56
Fontanière, S., Tost, J., Wierinckx, A., Lachuer, J., Lu, J., Hussein, N., Busato, F., Gut, I. G., Wang, Z.-Q., & Zhang, C. X. (2006) · Endocrine Related Cancer · doi:10.1677/erc.1.01294 · Cited by 56
Chen, J., Lippo, L., Labella, R., Tan, S. L., Marsden, B. D., Dustin, M. L., Ramasamy, S. K., & Kusumbe, A. P. (2020) · The EMBO Journal · doi:10.15252/embj.2020105242 · Cited by 58
Emerging role of protein kinase B/Akt signaling in pancreatic β-cell mass and function
Elghazi, L., Balcázar, N., & Bernal‐Mizrachi, E. (2006) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.01.005 · Cited by 55
Signaling Pathways Implicated in the Stimulation of β-Cell Proliferation by Extracellular Matrix
Parnaud, G., Hammar, E. B., Ribaux, P., Donath, M. Y., Berney, T., & Halban, P. A. (2009) · Molecular Endocrinology · doi:10.1210/me.2009-0008 · Cited by 56
Keefe, M., Wang, H., De La O, J.-P., Khan, A., Firpo, M. A., & Murtaugh, L. C. (2012) · Disease Models & Mechanisms · doi:10.1242/dmm.007799 · Cited by 54
Feng, Z., Li, J., Turco, B., Riopel, M., Yee, S., & Wang, R. (2012) · Diabetologia · doi:10.1007/s00125-012-2566-5 · Cited by 53
Regulation of beta cell replication
Lee, Y. C., & Nielsen, J. H. (2008) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2008.08.033 · Cited by 58
Podcheko, A., Northcott, P. A., Bikopoulos, G. J., Lee, A., Bommareddi, S. R., Kushner, J. A., Farhang-Fallah, J., & Rozakis-Adcock, M. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.02409-06 · Cited by 53
Self-citationAgudo, J., Ayuso, E., Jiménez, V., Salavert, A., Casellas, A., Tafuro, S., Haurigot, V., Ruberte, J., Segovia, J. C., Bueren, J. A., et al. (2008) · Diabetologia · doi:10.1007/s00125-008-1087-8 · Cited by 54
Limbert, C., Päth, G., Jakob, F. J., & Seufert, J. (2007) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2007.06.016 · Cited by 55
Su, Y., Jiang, X., Li, Y., Li, F., Cheng, Y., Peng, Y. H., Song, D., Hong, J., Ning, G., Cao, Y., et al. (2016) · Endocrinology · doi:10.1210/en.2016-1167 · Cited by 53
Wang, H.-L., Li, C.-Y., Zhang, B., Liu, Y.-D., Lu, B.-M., Shi, Z., An, N., Zhao, L.-K., Zhang, J.-J., Bao, J.-K., et al. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15059016 · Cited by 51
Rachdi, L., Balcázar, N., Elghazi, L., Barker, D. J., Krits, I., Kiyokawa, H., & Bernal‐Mizrachi, E. (2006) · Diabetes · doi:10.2337/db06-0861 · Cited by 51
Cyclin D2 Protein Stability Is Regulated in Pancreatic β-Cells
He, L. M., Sartori, D. J., Teta, M., Opare-Addo, L., Rankin, M. M., Long, S. Y., Diehl, J. A., & Kushner, J. A. (2009) · Molecular Endocrinology · doi:10.1210/me.2009-0057 · Cited by 49
Self-citationPTEN controls β‐cell regeneration in aged mice by regulating cell cycle inhibitor p16 ink4a
Zeng, N., Yang, K., Bayan, J., He, L., Aggarwal, R., Stiles, J. W., Hou, X., Medina, V., Abad, D., Palian, B. M., et al. (2013) · Aging Cell · doi:10.1111/acel.12132 · Cited by 50
Kim, S. Y., & Rane, S. G. (2011) · Development · doi:10.1242/dev.061481 · Cited by 53
TGF-β Signaling in Pancreatic Islet β Cell Development and Function
Lee, J., Lee, J.-H., & Rane, S. G. (2020) · Endocrinology · doi:10.1210/endocr/bqaa233 · Cited by 51
Regulation of Pdx1 by oxidative stress and Nrf2 in pancreatic beta-cells
Baumel-Alterzon, S., & Scott, D. K. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1011187 · Cited by 53
Molecular basis for the regulation of islet beta cell mass in mice: the role of E-cadherin
Wakae-Takada, N., Xuan, S., Watanabe, K., Meda, P., & Leibel, R. L. (2013) · Diabetologia · doi:10.1007/s00125-012-2824-6 · Cited by 48
Lakshmipathi, J., Álvarez-Pérez, J. C., Rosselot, C., Casinelli, G. P., Stamateris, R. E., Rausell-Palamos, F., O'Donnell, C. P., Vasavada, R. C., Scott, D. K., Alonso, L. C., et al. (2016) · Diabetes · doi:10.2337/db15-1398 · Cited by 47
Cózar‐Castellano, I., Haught, M., & Stewart, A. F. (2006) · Diabetes · doi:10.2337/db06-0627 · Cited by 49
Kawamori, D., Shirakawa, J., Liew, C. W., Hu, J., Morioka, T., Duttaroy, A., Burkey, B. F., & Kulkarni, R. (2017) · Diabetologia · doi:10.1007/s00125-017-4303-6 · Cited by 46
The regulation of pre- and post-maturational plasticity of mammalian islet cell mass
Mezza, T., & Kulkarni, R. (2014) · Diabetologia · doi:10.1007/s00125-014-3251-7 · Cited by 45
Åkerfeldt, M. C., & Laybutt, D. R. (2011) · Diabetes · doi:10.2337/db11-0083 · Cited by 45
New sources of pancreatic beta cells
Porat, S., & Dor, Y. (2007) · Current Diabetes Reports · doi:10.1007/s11892-007-0049-8 · Cited by 45
Chen, S., Shimoda, M., Chen, J., Matsumoto, S., & Grayburn, P. A. (2012) · Cell Cycle · doi:10.4161/cc.11.4.19120 · Cited by 46
Velázquez-García, S., Valle, S. R., Rosa, T. C., Takane, K. K., Demirci, C., Álvarez-Pérez, J. C., Mellado‐Gil, J. M., Ernst, S., Scott, D. K., Vasavada, R. C., et al. (2011) · Diabetes · doi:10.2337/db10-1783 · Cited by 46
Control of pancreatic β-cell fate by insulin signaling: The sweet spot hypothesis
Johnson, J. D., & Alejandro, E. U. (2008) · Cell Cycle · doi:10.4161/cc.7.10.5865 · Cited by 42
Nordentoft, I., Jeppesen, P. B., Hong, J., Abudula, R., & Hermansen, K. (2008) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf800504r · Cited by 44
Out of the cycle: Impact of cell cycle aberrations on cancer metabolism and metastasis
Cheung, A. H. K., Hui, C. H., Wong, K. Y., Liu, X., Chen, B., Kang, W., & To, K. F. (2022) · International Journal of Cancer · doi:10.1002/ijc.34288 · Cited by 47
Wang, Y., Liu, Y., Wang, H., Li, C., Qi, P., & Bao, J. (2012) · Experimental Biology and Medicine · doi:10.1258/ebm.2011.011251 · Cited by 44
Inhibition of Gsk3β activity improves β-cell function in c-Kit male mice
Feng, Z., Donnelly, L., Li, J., Krishnamurthy, M., Riopel, M., & Wang, R. (2012) · Laboratory Investigation · doi:10.1038/labinvest.2011.200 · Cited by 42
Postnatal β-Cell Proliferation and Mass Expansion Is Dependent on the Transcription Factor Nkx6.1
Taylor, B. L., Benthuysen, J. R., & Sander, M. (2014) · Diabetes · doi:10.2337/db14-0684 · Cited by 39
Insights from exome sequencing for endocrine disorders
de Bruin, C., & Dauber, A. N. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.72 · Cited by 38
Aging induces a distinct gene expression program in mouse islets
Rankin, M. M., & Kushner, J. A. (2010) · Islets · doi:10.4161/isl.2.6.13376 · Cited by 39
Self-citationmTORC1 pathway mediates beta cell compensatory proliferation in 60 % partial-pancreatectomy mice
Li, W., Zhang, H., Nie, A., Ni, Q., Li, F., Ning, G., Li, X., Gu, Y., & Wang, Q. (2016) · Endocrine · doi:10.1007/s12020-016-0861-5 · Cited by 37
A Simple Matter of Life and Death—The Trials of Postnatal Beta-Cell Mass Regulation
Tarabra, E., Pelengaris, S., & Khan, M. (2012) · International Journal of Endocrinology · doi:10.1155/2012/516718 · Cited by 38
MicroRNAs can effectively induce formation of insulin-producing cells from mesenchymal stem cells
Bai, C., Gao, Y., Li, X., Wang, K., Xiong, H., Shan, Z., Zhang, P., Wang, W., Guan, W., & Ma, Y. (2017) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2259 · Cited by 37
Liu, M., Peng, J., Tai, N., Pearson, J. A., Hu, C., Guo, J., Hou, L., Zhao, H., Wong, F. S., & Li, W. (2018) · Diabetologia · doi:10.1007/s00125-018-4705-0 · Cited by 36
Ghanaat‐Pour, H., Huang, Z., Lehtihet, M., & Sjöholm, Å. (2007) · Journal of Molecular Endocrinology · doi:10.1677/jme-07-0002 · Cited by 39
How to make pancreatic β cells — prospects for cell therapy in diabetes
Nir, T., & Dor, Y. (2005) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2005.07.005 · Cited by 36
Hsueh, B., Burns, V. M., Pauerstein, P. T., Holzem, K. M., Li, Y., Engberg, K., Wang, A.-C., Gu, X., Chakravarthy, H., Arda, H. E., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05614-4 · Cited by 35
Lee, J.-H., Jo, J., Hardikar, A. A., Periwal, V., & Rane, S. G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008653 · Cited by 37
Redifferentiation of Adult Human β Cells Expanded In Vitro by Inhibition of the WNT Pathway
Lenz, A., Toren-Haritan, G., & Efrat, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112914 · Cited by 35
Vasavada, R. C., Cózar‐Castellano, I., Sipula, D., & Stewart, A. F. (2006) · Diabetes · doi:10.2337/db06-0517 · Cited by 35
Update on the Protective Molecular Pathways Improving Pancreatic Beta-Cell Dysfunction
Puddu, A., Sanguineti, R., Mach, F., Dallegri, F., Viviani, G. L., & Montecucco, F. (2013) · Mediators of Inflammation · doi:10.1155/2013/750540 · Cited by 33
Alagpulinsa, D. A., Cao, J. J. L., Sobell, D., & Poznansky, M. C. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.08.011 · Cited by 33
Robertson, K., Kopchick, J. J., & Liu, J. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00378.2005 · Cited by 33
Márquez-Aguirre, A. L., Canales-Aguirre, A. A., Padilla‐Camberos, E., Esquivel‐Solís, H., & Diaz-Martinez, N. E. (2015) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x20154363 · Cited by 34
Metabolic Effects of Recurrent Genetic Aberrations in Multiple Myeloma
Bloedjes, T. A., de Wilde, G., & Guikema, J. E. J. (2021) · Cancers · doi:10.3390/cancers13030396 · Cited by 32
You, H., & Laychock, S. G. (2009) · Endocrinology · doi:10.1210/en.2009-0468 · Cited by 31
Hypothalamic Control of Prolactin Secretion, and the Multiple Reproductive Functions of Prolactin
Grattan, D. R., & Tissier, P. L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00012-0 · Cited by 31
Dachshund homologues play a conserved role in islet cell development
Kalousová, A., Mavropoulos, A., Adams, B. A., Nekrep, N., Li, Z., Krauß, S., Stainier, D. Y. R., & German, M. S. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.09.007 · Cited by 31
The Peroxide Dilemma: Opposing and Mediating Insulin Action
Szypowska, A. A., & Burgering, B. M. T. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3794 · Cited by 33
Repurposing cAMP-Modulating Medications to Promote β-Cell Replication
Zhao, Z., Low, Y., Armstrong, N., Kenty, J. H.-R., Sun, S. A., Arvanites, A. C., Hollister‐Lock, J., Shah, N. H., Weir, G. C., & Annes, J. P. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1120 · Cited by 30
Tamoxifen suppresses pancreatic β-cell proliferation in mice
Ahn, S.-H., Granger, A., Rankin, M. M., Lam, C. J., Cox, A. R., & Kushner, J. A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0214829 · Cited by 31
Self-citationPerinatal survivin is essential for the establishment of pancreatic beta cell mass in mice
Wu, X., Wang, L., Schroer, S. A., Choi, D., Chen, P., Okada, H., & Woo, M. (2009) · Diabetologia · doi:10.1007/s00125-009-1469-6 · Cited by 30
Loss of Foxd3 Results in Decreased β-Cell Proliferation and Glucose Intolerance During Pregnancy
Plank, J. L., Frist, A. Y., LeGrone, A. W., Magnuson, M. A., & Labosky, P. A. (2011) · Endocrinology · doi:10.1210/en.2010-1462 · Cited by 31
MafA Is Required for Postnatal Proliferation of Pancreatic β-Cells
Eto, K., Nishimura, W., Oishi, H., Udagawa, H., Kawaguchi, M., Hiramoto, M., Fujiwara, T., Takahashi, S., & Yasuda, K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104184 · Cited by 30
Harada, N., Yoda, Y., Yotsumoto, Y., Masuda, T., Takahashi, Y., Katsuki, T., Kai, K., Shiraki, N., Inui, H., & Yamaji, R. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00211.2017 · Cited by 29
Diminished Pancreatic β-Cell Mass in Securin-Null Mice Is Caused by β-Cell Apoptosis and Senescence
Chesnokova, V., Wong, C., Zonis, S., Gruszka, A., Wawrowsky, K., Ren, S.-G., Ben-Shlomo, A., & Yu, R. (2009) · Endocrinology · doi:10.1210/en.2008-0972 · Cited by 28
Ma, Z., Portwood, N., Brodin, D., Grill, V., & Björklund, A. (2007) · Diabetes · doi:10.2337/db06-0322 · Cited by 29
Islet Regeneration: Endogenous and Exogenous Approaches
Docherty, F. M., & Sussel, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073306 · Cited by 28
Arumugam, R., Fleenor, D. E., Lu, D., & Freemark, M. (2011) · Endocrinology · doi:10.1210/en.2010-1258 · Cited by 29
Chemical Methods to Induce Beta-Cell Proliferation
Vetere, A., & Wagner, B. K. (2012) · International Journal of Endocrinology · doi:10.1155/2012/925143 · Cited by 27
Orime, K., Shirakawa, J., Togashi, Y., Tajima, K., Inoue, H., Ito, Y., Sato, K., Nakamura, A., Aoki, K., Goshima, Y., et al. (2012) · Endocrinology · doi:10.1210/en.2012-1814 · Cited by 28
Urizar, A. I., Prause, M. C. B., Wortham, M., Sui, Y., Thams, P., Sander, M., Christensen, G. L., & Billestrup, N. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.110524 · Cited by 31
Tiwari, S., Roel, C., Wills, R. C., Casinelli, G. P., Tanwir, M., Takane, K. K., & Fiaschi‐Taesch, N. (2015) · Diabetes · doi:10.2337/db14-1885 · Cited by 27
Genetics of Type 2 Diabetes: the Power of Isolated Populations
Andersen, M. K., Pedersen, C. T., Moltke, I., Hansen, T. F., Albrechtsen, A., & Grarup, N. (2016) · Current Diabetes Reports · doi:10.1007/s11892-016-0757-z · Cited by 32
Vertical sleeve gastrectomy triggers fast β-cell recovery upon overt diabetes
Oppenländer, L., Palit, S., Stemmer, K., Greisle, T., Sterr, M., Salinno, C., Bastidas-Ponce, A., Feuchtinger, A., Böttcher, A., Ansarullah, M., et al. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101330 · Cited by 24
Stein, J. M., Milewski, W. M., Hara, M., Steiner, D. F., & Dey, A. (2011) · Islets · doi:10.4161/isl.3.1.14435 · Cited by 27
Schaffer, A. E., Yang, A., Thorel, F., Herrera, P. L., & Sander, M. (2011) · Molecular Endocrinology · doi:10.1210/me.2011-1010 · Cited by 26
The prolyl isomerase Pin1 increases β-cell proliferation and enhances insulin secretion
Nakatsu, Y., Mori, K., Matsunaga, Y., Yamamotoya, T., Ueda, K., Inoue, Y., Mitsuzaki-Miyoshi, K., Sakoda, H., Fujishiro, M., Yamaguchi, S., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.780726 · Cited by 26
Kang, J.-H., Kim, M.-J., Ko, S., Jeong, I., Koh, K.-H., Rhie, D.-J., Yoon, S.-K., Hahn, S. J., Kim, M.-S., & Jo, Y.-H. (2006) · Diabetologia · doi:10.1007/s00125-006-0179-6 · Cited by 26
Kayali, A. G., Lopez, A. D., Hao, E., Hinton, A. C., Hayek, A., & King, C. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038721 · Cited by 26
Arumugam, R., Fleenor, D., & Freemark, M. (2013) · Endocrine · doi:10.1007/s12020-013-0073-1 · Cited by 26
Oda, T., Taneichi, H., Takahashi, K., Togashi, H., Hangai, M., Nakagawa, R., Ono, M., Matsui, M., Sasai, T., Nagasawa, K., et al. (2014) · Diabetic Medicine · doi:10.1111/dme.12589 · Cited by 25
Metadata
- Authors
- Kushner, J. A., Ciemerych, M. A., Sicinska, E., Wartschow, L. M., Teta, M., Long, S. Y., Sicinski, P., & White, M. F.
- Affiliations
- Children's Hospital of Philadelphia (US)
- Harvard University (US)
- Department of Cancer Biology, Dana-Farber Cancer Institute and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115
- Howard Hughes Medical Institute (US)
- Corresponding author
- Kushner, Jake A.
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 2005-05-01
- Volume
- 25
- Issue
- 9
- Pages
- 3752-3762
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC1084308
- OpenAlex
- W1969459168
- Cited by
- 334
- References
- 32
- Citations by year
- 2026: 2 · 2025: 9 · 2024: 7 · 2023: 4 · 2022: 8 · 2021: 7 · 2020: 7 · 2019: 13 · 2018: 9 · 2017: 18 · 2016: 16 · 2015: 17 · 2014: 16 · 2013: 21 · 2012: 21
- FWCI
- 28.22
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular and Cellular Biology (publishedVersion)
- PubMed Central (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- Charles H. Hood Foundation
- Kosciuszko Foundation
- Pediatric Endocrine Society
- National Institutes of Health (5k11dk002024-02, DK38712)
- National Cancer Institute (R01CA083688)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK55326, DK 43808, R01DK055326, DK 38712, DK 02024, R01DK038712, DK 064101, K08DK064101, R01DK043808)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- cyclin D2, cyclin D1, cyclin D3, pancreatic beta-cell proliferation, beta-cell mass, impaired glucose tolerance, diabetes mellitus, CDK4, CDK6, G1 cell cycle, pancreatic islets
- MeSH terms
- Animals, Blood Glucose, Diabetes Mellitus, Glucagon, Insulin, Islets of Langerhans, Male, Gene Expression, Cyclins, Glucose Intolerance, Mice, Knockout, Cyclin D1, Cell Proliferation, Mice, Cyclin D2
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