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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.
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“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]
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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
Research works printed but not linked: 2
- 10.1172/JCI0214439 · DOI
- Sherr C. J, 2000, Cancer Res., 60, 3689
Cited by
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Kauri, L. M., Wang, G., Patrick, C., Bareggi, M., Hill, D. J., & Scott, F. W. (2007) · Laboratory Investigation · doi:10.1038/labinvest.3700687 · Cited by 24
Mouse Models of Cell Cycle Regulators: New Paradigms
Aleem, E. A., & Kaldis, P. (2006) · Springer eBooks · doi:10.1007/400_023 · Cited by 24
Adult-onset deletion of Pten increases islet mass and beta cell proliferation in mice
Yang, K., Bayan, J., Zeng, N., Aggarwal, R., He, L., Peng, Z., Kassa, A. D., Kim, M., Luo, Z., Shi, Z., et al. (2013) · Diabetologia · doi:10.1007/s00125-013-3085-8 · Cited by 21
Blandino-Rosano, M., Alejandro, E. U., Sathyamurthy, A., Scheys, J. O., Gregg, B. S., Chen, A. Y., Rachdi, L., Weiss, A., Barker, D. J., Gould, A. P., et al. (2012) · Diabetologia · doi:10.1007/s00125-012-2465-9 · Cited by 21
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Crawford, L. W., Ables, E. T., Oh, Y. A., Boone, B. E., Levy, S., & GANNON, M. A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001611 · Cited by 21
Insulin Receptor Substrate-2 in β-Cells Decreases Diabetes in Nonobese Diabetic Mice
Norquay, L., D’Aquino, K. E., Opare-Addo, L., Kuznetsova, A., Haas, M., Bluestone, J. A., & White, M. F. (2009) · Endocrinology · doi:10.1210/en.2009-0395 · Cited by 22
Self-citationEnhancing Pancreatic Beta-Cell Regeneration In Vivo with Pioglitazone and Alogliptin
Yin, H., Park, S. Y., Wang, X., Misawa, R., Grossman, E. J., Tao, J., Zhong, R., Witkowski, P., Bell, G. I., & Chong, A. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065777 · Cited by 22
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Liang, Y., Tan, A., Liang, D., Yang, X., Liao, M., Gao, Y., Jiang, Y., Yao, Z., Lin, X., Lu, Z., et al. (2015) · Journal of Diabetes Investigation · doi:10.1111/jdi.12439 · Cited by 21
CDK4, pRB and E2F1: connected to insulin
Fajas, L., Blanchet, É., & Annicotte, J. (2010) · Cell Division · doi:10.1186/1747-1028-5-6 · Cited by 21
Hypophosphorylated pRb knock‐in mice exhibit hallmarks of aging and vitamin C‐preventable diabetes
Jiang, Z., Li, H., Schroer, S. A., Voisin, V., Ju, Y., Pacal, M., Erdmann, N., Shi, W., Chung, P. E. D., Deng, T., et al. (2022) · The EMBO Journal · doi:10.15252/embj.2020106825 · Cited by 18
Regeneration in Liver and Pancreas: Time to Cut the Umbilical Cord?
Dor, Y., & Stanger, B. Z. (2007) · Science s STKE · doi:10.1126/stke.4142007pe66 · Cited by 18
Sfrp5 mediates glucose-induced proliferation in rat pancreatic β-cells
Guan, B., Li, W., Li, F., Xie, Y., Ni, Q., Gu, Y., Li, X., Wang, Q., Zhang, H., & Ning, G. (2016) · Journal of Endocrinology · doi:10.1530/joe-15-0535 · Cited by 20
Chen, X., Zhang, X., Chen, F., Larson, C. S., Wang, L.-J., & Kaufman, D. B. (2009) · Transplantation · doi:10.1097/tp.0b013e3181b0d2ee · Cited by 20
Li, Y., Chen, Y., Liu, Z., Lin, B., Deng, X., Xiao, Q., Chen, Z., Ye, H., Chen, D., Su, Y., et al. (2022) · Acta Diabetologica · doi:10.1007/s00592-022-01871-6 · Cited by 19
Pancreas β cell regeneration and type 1 diabetes (Review)
Wu, J.-X., Yang, X., Chen, B., & Xu, X. (2014) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2014.2163 · Cited by 20
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Sartori, D. J., Wilbur, C. J., Long, S. Y., Rankin, M. M., Li, C., Bradfield, J. P., Hakonarson, H. H., Grant, S. F. A., Pu, W. T., & Kushner, J. A. (2013) · Molecular Endocrinology · doi:10.1210/me.2013-1265 · Cited by 19
Self-citationTenenbaum, M., Plaisance, V., Boutry, R., Pawlowski, V., Jacovetti, C., Sanchez-Parra, C., Ezanno, H., Bourry, J., Beeler, N., Pasquetti, G., et al. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03499-7 · Cited by 19
Murine pituitary tumor-transforming gene functions as a securin protein in insulin-secreting cells
Yu, R., Cruz-Soto, M. E., Calzi, S. L., Hui, H., & Melmed, S. K. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06885 · Cited by 19
Chen, S.-S., Jiang, T., Wang, Y., Gu, L.-Z., Wu, H., Tan, L., & Guo, J. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.12.051 · Cited by 18
Cannabinoids Regulate Bcl-2 and Cyclin D2 Expression in Pancreatic β Cells
Kim, J., Lee, K. J., Kim, J. S., Rho, J. G., Shin, J. J., Song, W. K., Lee, E. K., Egan, J. M., & Kim, W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150981 · Cited by 18
Xu, W., Cui, J., Zhou, F., Bai, M., Deng, R., & Wang, W. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.05.184 · Cited by 18
Langfermann, D. S., Rößler, O. G., & Thiel, G. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.12.003 · Cited by 17
Giannattasio, S., Giacovazzo, G., Bonato, A., Caruso, C., Luvisetto, S., Coccurello, R., & Caruso, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-31090-5 · Cited by 15
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Hinault, C., Hu, J., Maier, B. F., Mirmira, R. G., & Kulkarni, R. (2008) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2008.00947.x · Cited by 16
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Wang, H., & Kumar, T. R. (2012) · Gene Expression Patterns · doi:10.1016/j.gep.2012.01.003 · Cited by 14
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Baumel-Alterzon, S., Katz, L. S., Lambertini, L., Tse, I., Heidery, F., Garcı́a-Ocaña, A., & Scott, D. K. (2024) · Diabetologia · doi:10.1007/s00125-023-06071-7 · Cited by 15
Fernández-Marcos, P. J., Pantoja, C., González‐Rodríguez, Á., Martin, N., Flores, J. M., Valverde, Á. M., Hara, E., & Serrano, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008744 · Cited by 15
Li, C., Sun, B., Fang, Q., Ding, M., Xing, Y.-Z., Chen, L., & Yu, D. M. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00326 · Cited by 15
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Tschen, S.-I., Zeng, C., Field, L. J., Dhawan, S., Bhushan, A., & Georgia, S. K. (2017) · Cell Cycle · doi:10.1080/15384101.2017.1319999 · Cited by 17
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Xing, B., Ma, J., Jiang, Z., Feng, Z., Ling, S., Szigety, K., Su, W., Zhang, L., Jia, R., Sun, Y., et al. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201805049 · Cited by 15
Mataraza, J., Tumang, J. R., Gumina, M. R., Gurdak, S. M., Rothstein, T. L., & Chiles, T. C. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.787 · Cited by 15
Molecular mechanism of activating protein-4 regulated growth of hepatocellular carcinoma
Ge, Z., Zhang, B., Bu, X., Wang, Y., Xiang, L., & Tan, J. (2014) · Tumor Biology · doi:10.1007/s13277-014-2562-0 · Cited by 14
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Gutteridge, A., Rukstalis, J. M., Ziemek, D., Tié, M., Ji, L., Ramos-Zayas, R., Nardone, N. A., Norquay, L., Brenner, M. B., Tang, K., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056024 · Cited by 14
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Mansouri, A. (2012) · ISRN Endocrinology · doi:10.5402/2012/640956 · Cited by 16
Nazari, Z., Nabiuni, M., Saeidi, M., & Golalipour, M. (2017) · Iranian Journal of Basic Medical Sciences · doi:10.22038/ijbms.2017.8240 · Cited by 14
Engler, D. (2007) · Acta bio-medica dell'Ateneo parmense/Acta biomedica · Cited by 15
Urizar, A. I., Prause, M. C. B., Ingerslev, L. R., Wortham, M., Sui, Y., Sander, M., Williams, K., Barrès, R., Larsen, M. R., Christensen, G. L., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05906-w · Cited by 13
Role of large MAF transcription factors in the mouse endocrine pancreas
Abdellatif, A. M., OGATA, K., Kudo, T., Xiafukaiti, G., Chang, Y.-H., Katoh, M., El-Morsy, S. E., Oishi, H., & Takahashi, S. (2015) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.15-0001 · Cited by 13
Wang, Q., Han, A., Chen, L., Sun, J., Lin, Z., Zhang, X., & Ren, X. (2019) · OncoTargets and Therapy · doi:10.2147/ott.s202698 · Cited by 13
Lavine, J. A., Raess, P. W., Davis, D. B., Rabaglia, M. E., Presley, B. K., Keller, M. P., Beinfeld, M. C., Kopin, A. S., Newgard, C. B., & Attie, A. (2008) · Molecular Endocrinology · doi:10.1210/me.2008-0255 · Cited by 14
RetractedFujino, R., Ishikawa, Y.-I., Tanaka, K., Kanatsu‐Shinohara, M., Tamura, K., Kogo, H., Shinohara, T., & Hara, T. (2006) · Molecular Reproduction and Development · doi:10.1002/mrd.20504 · Cited by 13
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Khalaileh, A., Gonen‐Gross, T., Magenheim, J., Nir, T., Porat, S., Salpeter, S. J., Stolovich-Rain, M., Swisa, A., Weinberg, N., & Dor, Y. (2008) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2008.00948.x · Cited by 12
Park, J. (2024) · Animal Bioscience · doi:10.5713/ab.23.0255 · Cited by 11
Saavedra-Ávila, N. A., Sengupta, U., Sánchez, B., Sala, E., Haba, L., Stratmann, T., Verdaguer, J., Mauricio, D., Mezquita, B., Ropero, A. B., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323236111 · Cited by 11
Chang, M. C., Xiao, S., & Nosé, V. (2007) · Human Pathology · doi:10.1016/j.humpath.2006.10.019 · Cited by 11
Agent-based modeling of the interaction between CD8+ T cells and Beta cells in type 1 diabetes
Ozturk, M. C., Xu, Q., & Çınar, A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0190349 · Cited by 11
Lessons from neonatal β-cell epigenomic for diabetes prevention and treatment
Abderrahmani, A., Jacovetti, C., & Regazzi, R. (2022) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2022.03.002 · Cited by 11
Staels, W., Berthault, C., Bourgeois, S., Laville, V., Lourenço, C., Leu, N. D., & Scharfmann, R. (2024) · Molecular Metabolism · doi:10.1016/j.molmet.2024.101990 · Cited by 11
Recombinant protein CCN5/WISP2 promotes islet cell proliferation and survival in vitro
Kaddour, N., Zhang, D., Gao, Z., & Liu, J. (2019) · Growth Factors · doi:10.1080/08977194.2019.1652400 · Cited by 10
Haploinsufficiency of Insm1 Impairs Postnatal Baseline β-Cell Mass
Tao, W., Zhang, Y., Ma, L., Deng, C., Duan, H., Liang, X., Liao, R., Lin, S., Nie, T., Chen, W., et al. (2018) · Diabetes · doi:10.2337/db17-1330 · Cited by 10
Diabetes Mellitus: An Opportunity for Therapy with Stem Cells?
Sordi, V., Bertuzzi, F., & Piemonti, L. (2008) · Regenerative Medicine · doi:10.2217/17460751.3.3.377 · Cited by 11
Pancreatic β-cell remodeling in health and aging: Lessons from rodents and humans
Darwish, R., Alcibahy, Y., Dhawan, S., Butler, A. E., & Moin, A. S. M. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102815 · Cited by 11
Wang, Y., Wu, H., Gao, L., Chen, S., Gu, L.-Z., Ding, Z., & Guo, J. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.07.003 · Cited by 9
Rassi, D. M., Junta, C. M., Fachin, A. L., Sandrin‐Garcia, P., Mello, S. S., Marques, M. M., Fernandes, A. P., Foss‐Freitas, M. C., Foss, M. C., Sakamoto‐Hojo, E. T., et al. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1375.026 · Cited by 9
The D-Type Cyclins: A Historical Perspective
Sherr, C. J., & Siciński, P. (2017) · Current cancer research · doi:10.1007/978-3-319-64451-6_1 · Cited by 9
CDK4 activity in mouse embryos expressing a single D-type cyclin
Ciemerych, M. A., Yu, Q., Szczepańska, K., & Siciński, P. (2008) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072336mc · Cited by 9
Self-citationKehm, R., Jähnert, M., Deubel, S., Flore, T., König, J., Jung, T., Stadion, M., Jonas, W., Schürmann, A., Grune, T., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101748 · Cited by 9
Interventions to improve β-cell mass and function
Mondal, P., Prasad, A., & Girdhar, K. (2017) · Annales d Endocrinologie · doi:10.1016/j.ando.2016.11.002 · Cited by 7
Let7b-5p inhibits insulin secretion and decreases pancreatic β-cell mass in mice
Ji, H., Fan, L., Shan, A., Wang, W., Ning, G., Cao, Y., & Jiang, X. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111506 · Cited by 7
Molecular and cellular key players in human islet transplantation
Hermann, M., Margreiter, R., & Hengster, P. (2007) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2007.00055.x · Cited by 8
Nino‐Fong, R., Fatehi‐Hassanabad, Z., Lee, S. C., Lu, H., Wheeler, M. B., & Chan, C. B. (2011) · Journal of Molecular Endocrinology · doi:10.1530/jme-10-0117 · Cited by 8
Bone metabolism: a note on the significance of mouse models
Raška, O., Bernášková, K., & Raška, I. (2009) · Physiological Research · doi:10.33549/physiolres.931459 · Cited by 8
Halter, J. B. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00017-8 · Cited by 8
Betacellulin ameliorates hyperglycemia in obese diabetic db/db mice
Oh, Y. S., Shin, S., Li, H. Y., Park, E.-Y., Lee, S. M., Choi, C. S., Lim, Y., Jung, H. S., & Jun, H. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1303-1 · Cited by 8
Harnessing beta-cell replication: advancing molecular insights to regenerative therapies in diabetes
Vasavada, R. C., & Dhawan, S. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1612576 · Cited by 6
Towards the recognition of oligogenic forms of type 2 diabetes
Collen, L. L., Froguel, P., & Bonnefond, A. (2024) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2024.06.006 · Cited by 6
Pancreatic cells and their progenitors.
Salpeter, S., & Dor, Y. (2006) · Methods in Enzymology · doi:10.1016/s0076-6879(06)19013-8 · Cited by 5
CXXC4 mediates glucose-induced β-cell proliferation
Guan, B., Zhan, Z., Wang, L., Wang, L., & Liu, L. (2020) · Acta Diabetologica · doi:10.1007/s00592-020-01525-5 · Cited by 6
Fritz, M., Korade, Ž., Nylander, K. D., & Schor, N. F. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.06.029 · Cited by 6
Incorporating Type 1 Diabetes Prevention Into Clinical Practice
Gregory, J. M., Lilley, J. S., Misfeldt, A. A., Buscariollo, D. L., Russell, W. E., & Moore, D. J. (2010) · Clinical Diabetes · doi:10.2337/diaclin.28.2.61 · Cited by 6
Iida, R., Ueki, M., & Yasuda, T. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2021.166318 · Cited by 5
Hwang, Y. J., Jung, G., Jeon, W. B., & Lee, K. (2020) · Heliyon · doi:10.1016/j.heliyon.2020.e04918 · Cited by 5
Pancreatic β‐cell turnover in health and disease
Alcibahy, Y., Darwish, R., Butler, A. E., & Moin, A. S. M. (2025) · Diabetes Obesity and Metabolism · doi:10.1111/dom.70191 · Cited by 5
Lin, Z., Zhao, Y., Song, L., Mu, K., Zhang, M., Liu, H., Li, X., Zhao, J., Wang, C., & Jia, W. (2016) · Molecular Medicine · doi:10.2119/molmed.2015.00155 · Cited by 4
Mammalian Development and Cancer: A Brief History of Mice Lacking D-Type Cyclins or CDK4/CDK6
Kalaszczyńska, I., & Ciemerych, M. A. (2017) · Current cancer research · doi:10.1007/978-3-319-64451-6_2 · Cited by 4
Self-citationNoncanonical CDK4 signaling rescues diabetes in a mouse model by promoting β cell differentiation
Stamateris, R. E., Landa-Galván, H. V., Sharma, R. B., Darko, C., Redmond, D., Rane, S. G., & Alonso, L. C. (2023) · Journal of Clinical Investigation · doi:10.1172/jci166490 · Cited by 3
Cyclin-Dependent Kinases and Their Regulators as Potential Targets for Anticancer Therapeutics
Malumbres, M. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-470-4_10 · Cited by 3
Li, X., Xue, B., Wang, X., Sun, L., Zhang, T., Qu, L., Zou, X., & Mu, Y. (2012) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-012-0034-6 · Cited by 3
The Role of PTEN in β-Cell Growth
Stiles, B. L. (2010) · The Open Endocrinology Journal · doi:10.2174/1874216501004010023 · Cited by 3
New insights into genetic comorbidity mechanisms: type 2 diabetes and primary open-angle glaucoma
Wang, Y., Tian, Y., Quan, Y., Zhou, S., Dang, Y., Zhang, X., & Pei, C. (2025) · BMJ Open Ophthalmology · doi:10.1136/bmjophth-2025-002219 · Cited by 2
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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
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