The FoxO transcription factors and metabolic regulation
Open accessAbstract
Forkhead transcription factors FoxOs are conserved beyond species and regulated by insulin signaling pathway. FoxOs have diverse functions on differentiation, proliferation and cell survival. In calorie restriction (CR) or starvation, FoxOs are in nucleus, active transcriptionally, and increase hepatic glucose production, decrease insulin secretion, increase food intake and cause degradation of skeletal muscle for supplying substrates for glucose production. However, even in insulin resistance due to excessive calorie intake, FoxOs are active and causes type 2 diabetes and hyperlipidemia. The understanding of molecular mechanism how FoxOs affect glucose or lipid metabolism will shed light on the novel therapy of type 2 diabetes and the metabolic syndrome.
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
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 elderly participants, training significantly reduced inflammatory markers without changes in BMI or body fat.
“Several training interventions have not produced changes in basal IL-6 or CRP concentrations (213 -218) , while significant reductions in inflammatory markers have been observed following training without changes in BMI or body fat in elderly participants (219,220) .”
From Dietary factors and low-grade inflammation in relation to overweight and obesity (2011) · cites this paper as [219]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The pathogenesis of atherosclerosis: a perspective for the 1990s
Ross, R. (1993) · Nature · doi:10.1038/362801a0 · Cited by 10,618 · see citing works
Akt Promotes Cell Survival by Phosphorylating and Inhibiting a Forkhead Transcription Factor
Brunet, A., Bonni, A., Zigmond, M. J., Lin, M. Z., Juo, P., Hu, L. S., Anderson, M. J., Arden, K. C., Blenis, J., & Greenberg, M. E. (1999) · Cell · doi:10.1016/s0092-8674(00)80595-4 · Cited by 6,535 · see citing works
The phosphoinositide 3-kinase pathway
Cantley, L. C. (2002) · Science · doi:10.1126/science.296.5573.1655 · Cited by 5,621 · see citing works
The Wnt Signaling Pathway in Development and Disease
Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325 · see citing works
Abdominal obesity and metabolic syndrome
Després, J.-P., & Lemieux, I. (2006) · Nature · doi:10.1038/nature05488 · Cited by 4,354 · see citing works
Wnt signalling in stem cells and cancer
Reya, T., & Clevers, H. (2005) · Nature · doi:10.1038/nature03319 · Cited by 3,666 · see citing works
Identification of ubiquitin ligases required for skeletal muscle atrophy.
Bodine, S. C., Latres, E., Baumhueter, S., Lai, V. K.-M., Nunez, L., Clarke, B. A., Poueymirou, W. T., Panaro, F. J., Na, E., Dharmarajan, K., et al. (2001) · Science · doi:10.1126/science.1065874 · Cited by 3,521 · see citing works
Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase
Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510 · see citing works
Molecular Regulation of Vascular Smooth Muscle Cell Differentiation in Development and Disease
Owens, G. K., Kumar, M. S., & Wamhoff, B. R. (2004) · Physiological Reviews · doi:10.1152/physrev.00041.2003 · Cited by 3,472 · see citing works
Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase
Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239 · see citing works
Nutrient control of glucose homeostasis through a complex of PGC-1α and SIRT1
Rodgers, J. T., Lerin, C., Haas, W., Gygi, S. P., Spiegelman, B. M., & Puigserver, P. (2005) · Nature · doi:10.1038/nature03354 · Cited by 3,160 · see citing works
Sandri, M., Sandri, C., Gilbert, A., Skurk, C., Calabria, E., Picard, A., Walsh, K., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2004) · Cell · doi:10.1016/s0092-8674(04)00400-3 · Cited by 3,012 · see citing works
Liu, J.-P., Baker, J. C., Perkins, A. S., Robertson, E. J., & Efstratiadis, A. (1993) · Cell · doi:10.1016/s0092-8674(05)80084-4 · Cited by 2,854 · see citing works
Bodine, S. C., Stitt, T. N., Gonzalez, M., Kline, W. O., Stover, G. L., Bauerlein, R., Zlotchenko, E., Scrimgeour, A., Lawrence, J. C., Glass, D. J., et al. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-1014 · Cited by 2,752 · see citing works
Obesity and the regulation of energy balance
Spiegelman, B. M., & Flier, J. S. (2001) · Cell · doi:10.1016/s0092-8674(01)00240-9 · Cited by 2,398 · see citing works
Role of Brain Insulin Receptor in Control of Body Weight and Reproduction
Brüning, J. C., Gautam, D., Burks, D. J., Gillette, J., Schubert, M., Orban, P. C., Klein, R., Krone, W., Müller-Wieland, D., & Kahn, C. R. (2000) · Science · doi:10.1126/science.289.5487.2122 · Cited by 2,235 · see citing works
Stitt, T. N., Drujan, D., Clarke, B. A., Panaro, F., Timofeyva, Y., Kline, W. O., Gonzalez, M., Yancopoulos, G. D., & Glass, D. J. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00211-4 · Cited by 1,964 · see citing works
Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-γ
Picard, F., Kurtev, M. V., Chung, N., Topark‐Ngarm, A., Senawong, T., de Oliveira, R. M., Leid, M. E., McBurney, M. W., & Guarente, L. (2004) · Nature · doi:10.1038/nature02583 · Cited by 1,943 · see citing works
Ogg, S., Paradis, S., Gottlieb, S., Patterson, G. I., Lee, L., Tissenbaum, H. A., & Ruvkun, G. (1997) · Nature · doi:10.1038/40194 · Cited by 1,935 · see citing works
Increased dosage of a sir-2 gene extends lifespan in Caenorhabditis elegans
Tissenbaum, H. A., & Guarente, L. (2001) · Nature · doi:10.1038/35065638 · Cited by 1,918 · see citing works
Inhibition of Adipogenesis by Wnt Signaling
Ross, S. E., Hemati, N., Longo, K. A., Bennett, C. N., Lucas, P. C., Erickson, R. L., & MacDougald, O. A. (2000) · Science · doi:10.1126/science.289.5481.950 · Cited by 1,876 · see citing works
Disruption of IRS-2 causes type 2 diabetes in mice
Withers, D., Gutiérrez, J., Towery, H., Burks, D., Ren, J.-M., Previs, S., Zhang, Y., Bernal, D., Pons, S., Shulman, G., et al. (1998) · Nature · doi:10.1038/36116 · Cited by 1,850 · see citing works
Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1
Yoon, J. C., Puigserver, P., Chen, G., Donovan, J., Wu, Z., Rhee, J., Adelmant, G., Stafford, J., Kahn, C. R., Granner, D. K., et al. (2001) · Nature · doi:10.1038/35093050 · Cited by 1,821 · see citing works
FoxOs Are Critical Mediators of Hematopoietic Stem Cell Resistance to Physiologic Oxidative Stress
Tothova, Z., Kollipara, R., Huntly, B. J., Lee, B. H., Castrillon, D. H., Cullen, D. E., McDowell, E. P., Lazo-Kallanian, S., Williams, I. R., Sears, C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.01.003 · Cited by 1,562 · see citing works
SKP2 is required for ubiquitin-mediated degradation of the CDK inhibitor p27
Carrano, A. C., Eytan, E., Hershko, A., & Pagano, M. (1999) · Nature Cell Biology · doi:10.1038/12013 · Cited by 1,544 · see citing works
Lin, K., Dorman, J. B., Rodan, A. R., & Kenyon, C. J. (1997) · Science · doi:10.1126/science.278.5341.1319 · Cited by 1,496 · see citing works
Insulin-regulated hepatic gluconeogenesis through FOXO1–PGC-1α interaction
Puigserver, P., Rhee, J., Donovan, J., Walkey, C. J., Yoon, J. C., Oriente, F., Kitamura, Y., Altomonte, J., Dong, H., Accili, D., et al. (2003) · Nature · doi:10.1038/nature01667 · Cited by 1,487 · see citing works
CREB regulates hepatic gluconeogenesis through the coactivator PGC-1
Herzig, S., Long, F., Jhala, U. S., Hedrick, S., Quinn, R., Bauer, A., Rudolph, D., Schutz, G., Yoon, C., Puigserver, P., et al. (2001) · Nature · doi:10.1038/35093131 · Cited by 1,440 · see citing works
Bai, C., Sen, P., Hofmann, K., Ma, L., Goebl, M. G., Harper, J. W., & Elledge, S. J. (1996) · Cell · doi:10.1016/s0092-8674(00)80098-7 · Cited by 1,421 · see citing works
(2004) · doi:10.1016/s0092-8674(04)00452-0 · Cited by 1,356 · see citing works
Mammalian SIRT1 Represses Forkhead Transcription Factors
Motta, M. C., Divecha, N., Lemieux, M. E., Kamel, C., Chen, D., Gu, W. J., Bultsma, Y., McBurney, M. W., & Guarente, L. (2004) · Cell · doi:10.1016/s0092-8674(04)00126-6 · Cited by 1,351 · see citing works
FOXO transcription factors at the interface between longevity and tumor suppression
Greer, E. L., & Brunet, A. (2005) · Oncogene · doi:10.1038/sj.onc.1209086 · Cited by 1,306 · see citing works
Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5
Clark, K., Halay, E. D., Lai, E., & Burley, S. K. (1993) · Nature · doi:10.1038/364412a0 · Cited by 1,275 · see citing works
Unified nomenclature for the winged helix/forkhead transcription factorsPreprint
Kaestner, K. H., Knöchel, W., & Martínez, D. E. (2000) · Genes & Development · doi:10.1101/gad.14.2.142 · Cited by 1,162 · see citing works
Kulkarni, R., Brüning, J. C., Winnay, J. N., Postic, C., Magnuson, M. A., & Kahn, C. R. (1999) · Cell · doi:10.1016/s0092-8674(00)80546-2 · Cited by 1,148 · see citing works
Biggs, W., Meisenhelder, J., Hunter, T. R., Cavenee, W. K., & Arden, K. C. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.13.7421 · Cited by 1,116 · see citing works
FoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis
Paik, J.-H., Kollipara, R., Chu, G., Ji, H., Xiao, Y., Ding, Z., Miao, L., Tothova, Z., Horner, J. W., Carrasco, D. R., et al. (2007) · Cell · doi:10.1016/j.cell.2006.12.029 · Cited by 1,032 · see citing works
Lin, K., Hsin, H., Libina, N., & Kenyon, C. J. (2001) · Nature Genetics · doi:10.1038/88850 · Cited by 1,027 · see citing works
Suppression of Ovarian Follicle Activation in Mice by the Transcription Factor Foxo3a
Castrillón, D. H., Miao, L., Kollipara, R., Horner, J. W., & DePinho, R. A. (2003) · Science · doi:10.1126/science.1086336 · Cited by 956 · see citing works
Blüher, M., Michael, M. D., Peroni, O. D., Ueki, K., Carter, N., Kahn, B. B., & Kahn, C. R. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00199-5 · Cited by 806 · see citing works
FOXO transcription factor activation by oxidative stress mediated by the small GTPase Ral and JNK
Essers, M. A., Weijzen, S., de Vries‐Smits, A. M., Saarloos, I., de Ruiter, N. D., Bos, J. L., & Burgering, B. M. T. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600476 · Cited by 798 · see citing works
Phosphorylation of the Transcription Factor Forkhead Family Member FKHR by Protein Kinase B*
Rena, G., Guo, S., Cichy, S. C., Unterman, T., & Cohen, P. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.24.17179 · Cited by 787 · see citing works
Negative Regulation of the Forkhead Transcription Factor FKHR by Akt
Tang, E., Núñez, G., Barr, F. G., & Guan, K. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.24.16741 · Cited by 761 · see citing works
Functional Interaction Between ß-Catenin and FOXO in Oxidative Stress Signaling
Essers, M. A. G., Smits, L. M. M., Barker, N., Polderman, P. E., Burgering, B. M. T., & Korswagen, H. C. (2005) · Science · doi:10.1126/science.1109083 · Cited by 741 · see citing works
The Forkhead Transcription Factor Foxo1 Regulates Adipocyte Differentiation
Nakae, J., Kitamura, T., Kitamura, Y., Biggs, W., Arden, K. C., & Accili, D. (2003) · Developmental Cell · doi:10.1016/s1534-5807(02)00401-x · Cited by 727 · see citing works
Self-citationDecreasing hypothalamic insulin receptors causes hyperphagia and insulin resistance in rats
Obici, S., Feng, Z., Karkanias, G., Baskin, D. G., & Rossetti, L. (2002) · Nature Neuroscience · doi:10.1038/nn0602-861 · Cited by 719 · see citing works
Smith, J. S., Brachmann, C. B., Celic, I., Kenna, M. A., Muhammad, S., Starai, V. J., Avalos, J. L., Escalante-Semerena, J. C., Grubmeyer, C., Wolberger, C., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.12.6658 · Cited by 718 · see citing works
Sirt1 Regulates Insulin Secretion by Repressing UCP2 in Pancreatic β Cells
Bordone, L., Motta, M. C., Picard, F., Robinson, A., Jhala, U. S., Apfeld, J., McDonagh, T., Lemieux, M., McBurney, M., Szilvasi, A., et al. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0040031 · Cited by 715 · see citing works
Signalling pathways that mediate skeletal muscle hypertrophy and atrophy
Glass, D. J. (2003) · Nature Cell Biology · doi:10.1038/ncb0203-87 · Cited by 694 · see citing works
Hosaka, T., Biggs, W., Tieu, D. D., Boyer, A. D., Varki, N. M., Cavenee, W. K., & Arden, K. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400093101 · Cited by 684 · see citing works
Nakae, J., Kitamura, T., Silver, D. L., & Accili, D. (2001) · Journal of Clinical Investigation · doi:10.1172/jci12876 · Cited by 652 · see citing works
Self-citationNakae, J., Kitamura, T., Silver, D. L., & Accili, D. (2001) · Journal of Clinical Investigation · doi:10.1172/jci200112876 · Cited by 652 · see citing works
Self-citationColeman, M. E., DeMayo, F., Yin, K. C., Lee, H. M., Geske, R., Montgomery, C., & Schwartz, R. J. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.20.12109 · Cited by 642 · see citing works
Moynihan, K. A., Grimm, A. A., Plueger, M. M., Bernal‐Mizrachi, E., Ford, E. L., CRAS-MÉNEUR, C. M. H., Permutt, M. A., & Imai, S. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.07.001 · Cited by 630 · see citing works
Matsumoto, M., Pocai, A., Rossetti, L., DePinho, R. A., & Accili, D. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.08.006 · Cited by 616 · see citing works
Nakae, J., Biggs, W., Kitamura, T., Cavenee, W. K., Wright, C. V. E., Arden, K. C., & Accili, D. (2002) · Nature Genetics · doi:10.1038/ng890 · Cited by 616 · see citing works
Self-citationPuig, Ó., Marr, M. T., Ruhf, M.-L., & Tjian, R. (2003) · Genes & Development · doi:10.1101/gad.1098703 · Cited by 612 · see citing works
Daitoku, H., Hatta, M., Matsuzaki, H., Aratani, S., Ohshima, T., Miyagishi, M., Nakajima, T., & Fukamizu, A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400593101 · Cited by 602 · see citing works
Serum response factor: toggling between disparate programs of gene expression
Miano, J. M. (2003) · Journal of Molecular and Cellular Cardiology · doi:10.1016/s0022-2828(03)00110-x · Cited by 588 · see citing works
Kitamura, T., Nakae, J., Kitamura, Y., Kido, Y., Biggs, W., Wright, C. V. E., White, M. F., Arden, K. C., & Accili, D. (2002) · Journal of Clinical Investigation · doi:10.1172/jci16857 · Cited by 578 · see citing works
Self-citationKamei, Y., Miura, S., SUZUKI, M. T., Kai, Y., Mizukami, J., Taniguchi, T., Mochida, K., Tomoko, H. A. T. A., Matsuda, J., Aburatani, H., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400674200 · Cited by 574 · see citing works
Decreasing hypothalamic insulin receptors causes hyperphagia and insulin resistance in rats
Obici, S., Feng, Z., Karkanias, G. B., et al. (2002) · Nature Neuroscience · doi:10.1038/nn861 · Cited by 572 · see citing works
14-3-3 transits to the nucleus and participates in dynamic nucleocytoplasmic transport
Brunet, A., Kanai, F., Stehn, J. R., Xu, J., Sarbassova, D. A., Frangioni, J. V., Dalal, S. N., DeCaprio, J. A., Greenberg, M. E., & Yaffe, M. B. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200112059 · Cited by 562 · see citing works
Frescas, D., Valenti, L. N., & Accili, D. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m412357200 · Cited by 554 · see citing works
FoxO1 protects against pancreatic β cell failure through NeuroD and MafA induction
Kitamura, Y., Kitamura, T., Kruse, J.-P., Raum, J. C., Stein, R. W., Gu, W. J., & Accili, D. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.08.004 · Cited by 552 · see citing works
Kubota, N., Tobe, K., Terauchi, Y., Eto, K., Yamauchi, T., Suzuki, R., Tsubamoto, Y., Komeda, K., Nakano, R., Miki, H., et al. (2000) · Diabetes · doi:10.2337/diabetes.49.11.1880 · Cited by 550 · see citing works
Regulation of gene expression by insulin
O’Brien, R. M., & Granner, D. K. (1996) · Physiological Reviews · doi:10.1152/physrev.1996.76.4.1109 · Cited by 547 · see citing works
FOXO4 Is Acetylated upon Peroxide Stress and Deacetylated by the Longevity Protein hSir2
van der Horst, A., Tertoolen, L. G. J., Smits, L. M. M., Frye, R. A., Medema, R. H., & Burgering, B. M. T. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401138200 · Cited by 541 · see citing works
Wang, M. C., Bohmann, D., & Jasper, H. (2005) · Cell · doi:10.1016/j.cell.2005.02.030 · Cited by 537 · see citing works
Insulin-induced phosphorylation of FKHR (Foxo1) targets to proteasomal degradation
Matsuzaki, H., Daitoku, H., Hatta, M., Tanaka, K., & Fukamizu, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1934283100 · Cited by 534 · see citing works
Oh, S. W., Mukhopadhyay, A., Svrzikapa, N., Jiang, F., Davis, R. J., & Tissenbaum, H. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500749102 · Cited by 531 · see citing works
Skp2 inhibits FOXO1 in tumor suppression through ubiquitin-mediated degradation
Huang, H., Regan, K. M., Wang, F., Wang, D., Smith, D. I., van Deursen, J. M. A., & Tindall, D. J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406789102 · Cited by 519 · see citing works
Interacting genes in nematode dauer larva formation
Riddle, D. L., Swanson, M. M., & Albert, P. S. (1981) · Nature · doi:10.1038/290668a0 · Cited by 518 · see citing works
FoxO1 Regulates Multiple Metabolic Pathways in the Liver
Zhang, W., Patil, S., Chauhan, B., Guo, S., Powell, D. R., Le, J., Klotsas, A., Matika, R. W., Xiao, X., Franks, R. R., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600272200 · Cited by 517 · see citing works
Acetylation of Foxo1 alters its DNA-binding ability and sensitivity to phosphorylation
Matsuzaki, H., Daitoku, H., Hatta, M., Aoyama, H., Yoshimochi, K., & Fukamizu, A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502738102 · Cited by 479 · see citing works
Kitamura, T., Nakae, J., Kitamura, Y., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci200216857 · Cited by 479 · see citing works
Self-citationNakae, J., Park, B., & Accili, D. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.23.15982 · Cited by 474 · see citing works
Self-citationHow does calorie restriction work?Preprint
Koubova, J., & Guarente, L. (2003) · Genes & Development · doi:10.1101/gad.1052903 · Cited by 457 · see citing works
IRS-2 pathways integrate female reproduction and energy homeostasis
Burks, D. J., de Mora, J. F., Schubert, M., Withers, D. J., Myers, M. G., Towery, H. H., Altamuro, S. L., Flint, C. L., & White, M. F. (2000) · Nature · doi:10.1038/35030105 · Cited by 455 · see citing works
Forkhead protein FoxO1 mediates Agrp-dependent effects of leptin on food intake
Kitamura, T., Feng, Y., Kitamura, Y., Chua, S. C., Xu, A. W., Barsh, G. S., Rossetti, L., & Accili, D. (2006) · Nature Medicine · doi:10.1038/nm1392 · Cited by 449 · see citing works
Matsumoto, M. (2006) · Journal of Clinical Investigation · doi:10.1172/jci27047 · Cited by 430 · see citing works
PI3K integrates the action of insulin and leptin on hypothalamic neurons
Xu, A. W. (2005) · Journal of Clinical Investigation · doi:10.1172/jci200524301 · Cited by 420 · see citing works
Non-ageing developmental variant of Caenorhabditis elegans
Klass, M. R., & Hirsh, D. (1976) · Nature · doi:10.1038/260523a0 · Cited by 380 · see citing works
Kulkarni, R. N., Holzenberger, M., Shih, D. Q., Özcan, U., Stoffel, M., Magnuson, M. A., & Kahn, C. R. (2002) · Nature Genetics · doi:10.1038/ng872 · Cited by 363 · see citing works
The role of endothelial insulin signaling in the regulation of vascular tone and insulin resistance
Vicent, D., Ilany, J., Kondo, T., Naruse, K., Fisher, S. J., Kisanuki, Y. Y., Bursell, S. E., Yanagisawa, M., King, G. L., & Kahn, C. R. (2003) · Journal of Clinical Investigation · doi:10.1172/jci15211 · Cited by 355 · see citing works
FoxO6, a Novel Member of the FoxO Class of Transcription Factors with Distinct Shuttling Dynamics
Jacobs, F. M. J., van der Heide, L. P., Wijchers, P. J., Burbach, J. P. H., Hoekman, M. F. M., & Smidt, M. P. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302804200 · Cited by 341 · see citing works
Abnormal Angiogenesis in Foxo1 (Fkhr)-deficient Mice
Furuyama, T., Kitayama, K., Shimoda, Y., Ogawa, M., Sone, K., Yoshida-Araki, K., Hisatsune, H., Nishikawa, S.-I., Nakayama, K., Nakayama, K., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m314214200 · Cited by 336 · see citing works
Role of hypothalamic Foxo1 in the regulation of food intake and energy homeostasis
Kim, M.-S., Pak, Y. K., Jang, P., NamKoong, C., Choi, Y.-S., Won, J. C., Kim, K., Kim, S., Kim, H.-S., Park, J., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1731 · Cited by 333 · see citing works
Furuyama, T., Kitayama, K., Yamashita, H., & Mori, N. (2003) · Biochemical Journal · doi:10.1042/bj20030022 · Cited by 326 · see citing works
Daly, C., Wong, V., Burova, E., Wei, Y., Zabski, S. M., Griffiths, J., Lai, K. V., Lin, H. C., Ioffe, E., Yancopoulos, G. D., et al. (2004) · Genes & Development · doi:10.1101/gad.1189704 · Cited by 326 · see citing works
SREBPs suppress IRS-2-mediated insulin signalling in the liver
Ide, T., Shimano, H., Yahagi, N., Matsuzaka, T., Nakakuki, M., Yamamoto, T., Nakagawa, Y., Takahashi, A., Suzuki, H., Sone, H., et al. (2004) · Nature Cell Biology · doi:10.1038/ncb1111 · Cited by 321 · see citing works
Dysregulation of insulin receptor substrate 2 in β cells and brain causes obesity and diabetes
Lin, X., Taguchi, A., Park, S., Kushner, J. A., Li, F., Li, Y., & White, M. F. (2004) · Journal of Clinical Investigation · doi:10.1172/jci22217 · Cited by 313 · see citing works
Brownawell, A. M., Kops, G. J. P. L., Macara, I. G., & Burgering, B. M. T. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.10.3534-3546.2001 · Cited by 313 · see citing works
Foxo1 mediates insulin action on apoC-III and triglyceride metabolism
Altomonte, J., Lin, C., Harbaran, S., Richter, A. M., Xu, J., Meseck, M. L., & Dong, H. H. (2004) · Journal of Clinical Investigation · doi:10.1172/jci19992 · Cited by 310 · see citing works
Degradation of p57 Kip2 mediated by SCF Skp2 -dependent ubiquitylation
Kamura, T., Hara, T., Kotoshiba, S., Yada, M., Ishida, N., Imaki, H., Hatakeyama, S., Nakayama, K., & Nakayama, K. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1831009100 · Cited by 294 · see citing works
Forkhead transcription factors: new insights into protein kinase B (c-akt) signaling
Kops, G. J. P. L., & Burgering, B. M. T. (1999) · Journal of Molecular Medicine · doi:10.1007/s001099900050 · Cited by 286 · see citing works
Woods, Y. L., Rena, G., MORRICE, N. A., Barthel, A., Becker, W. B., Guo, S., Unterman, T. G., & Cohen, P. (2001) · Biochemical Journal · doi:10.1042/bj3550597 · Cited by 265 · see citing works
Tedesco, D., Lukas, J., & Reed, S. I. (2002) · Genes & Development · doi:10.1101/gad.1011202 · Cited by 261 · see citing works
Rena, G., Prescott, A. R., Guo, S., Cohen, P., & Unterman, T. G. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3540605 · Cited by 261 · see citing works
Foxo1 mediates insulin action on apoC-III and triglyceride metabolism
Altomonte, J., Lin, C., Harbaran, S., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200419992 · Cited by 260 · see citing works
Eisenmann, D. M., Maloof, J., Simske, J. S., Kenyon, C. J., & Kim, S. K. (1998) · Development · doi:10.1242/dev.125.18.3667 · Cited by 256 · see citing works
Rena, G., Bain, J., Elliott, M., & Cohen, P. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400048 · Cited by 250 · see citing works
The role of insulin receptor substrate 2 in hypothalamic and β cell function
Choudhury, A. I., Heffron, H., Smith, M. A., Al‐Qassab, H., Xu, A. W., Selman, C., Simmgen, M., Clements, M., Claret, M., MacColl, G., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24445 · Cited by 241 · see citing works
Insulin receptor substrate 2 plays a crucial role in β cells and the hypothalamus
Kubota, N., Terauchi, Y., Tobe, K., Yano, W., Suzuki, R., Ueki, K., Takamoto, I., Satoh, H., Maki, T., Kubota, T., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21484 · Cited by 239 · see citing works
Aoki, M., Jiang, H., & Vogt, P. K. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405454101 · Cited by 234 · see citing works
Convergence of Peroxisome Proliferator-activated Receptor γ and Foxo1 Signaling Pathways
Dowell, P., Otto, T. C., Adi, S., & Lane, M. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m309069200 · Cited by 233 · see citing works
Ablation of PDK1 in pancreatic β cells induces diabetes as a result of loss of β cell mass
Hashimoto, N., Kido, Y., Uchida, T., Asahara, S., Shigeyama, Y., Matsuda, T., Takeda, A., Tsuchihashi, D., Nishizawa, A., Ogawa, W., et al. (2006) · Nature Genetics · doi:10.1038/ng1774 · Cited by 227 · see citing works
Inhibition of Foxo1 function is associated with improved fasting glycemia in diabetic mice
Altomonte, J., Richter, A. M., Harbaran, S., Suriawinata, J., Nakae, J., Thung, S. N., Meseck, M. L., Accili, D., & Dong, H. H. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00156.2003 · Cited by 227 · see citing works
Self-citationArmoni, M., Harel, C., Karni, S. M., Chen, H., Bar‐Yoseph, F., Ver, M. R., Quon, M. J., & Karnieli, E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600320200 · Cited by 224 · see citing works
Tseng, Y.-H., Butte, A. J., Kokkotou, E., Yechoor, V. K., Taniguchi, C. M., Kriauciunas, K. M., Cypess, A. M., Niinobe, M., Yoshikawa, K., Patti, M. E., et al. (2005) · Nature Cell Biology · doi:10.1038/ncb1259 · Cited by 222 · see citing works
Acquisition of increased hormone sensitivity during in vitro adipocyte development.
Rubin, C. S., Lai, E. K., & Rosen, O. M. (1977) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)40427-3 · Cited by 219 · see citing works
Cahill, C. M., Tzivion, G., Nasrin, N., Ogg, S., Dore, J., Ruvkun, G., & Alexander-Bridges, M. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010042200 · Cited by 219 · see citing works
Control of smooth muscle development by the myocardin family of transcriptional coactivators
Wang, D., & Olson, E. N. (2004) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2004.08.003 · Cited by 218 · see citing works
Essential Role of Insulin Receptor Substrate 1 (IRS-1) and IRS-2 in Adipocyte Differentiation
Miki, H., Yamauchi, T., Suzuki, R., Komeda, K., Tsuchida, A., Kubota, N., Terauchi, Y., Kamon, J., Kaburagi, Y., Matsui, J., et al. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.7.2521-2532.2001 · Cited by 214 · see citing works
Hribal, M. L., Nakae, J., Kitamura, T., Shutter, J. R., & Accili, D. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212107 · Cited by 203 · see citing works
Self-citationRena, G., Prescott, A. R., Shaodong, G. U. O., et al. (2001) · Biochemical Journal · doi:10.1042/bj3540605 · Cited by 199 · see citing works
Defective insulin secretion in pancreatic β cells lacking type 1 IGF receptor
Xuan, S., Kitamura, T., Nakae, J., Politi, K. A., Kido, Y., Fisher, P. E., Morroni, M., Cinti, S., White, M. F., Herrera, P. L., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15276 · Cited by 198 · see citing works
Self-citationInsulin-regulated gene expression
O’Brien, R. M., Streeper, R. S., Ayala, J. E., Stadelmaier, B. T., & Hornbuckle, L. A. (2001) · Biochemical Society Transactions · doi:10.1042/bst0290552 · Cited by 194 · see citing works
Phenotypic Modulation of Smooth Muscle Cells through Interaction of Foxo4 and Myocardin
Liu, Z.-P., Wang, Z., Yanagisawa, H., & Olson, E. N. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.05.017 · Cited by 192 · see citing works
Insulin-like Growth Factor-mediated Muscle Differentiation
Turečková, J., Wilson, E. M., Cappalonga, J. L., & Rotwein, P. S. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104991200 · Cited by 178 · see citing works
Samuel, V. T., Choi, C. S., Phillips, T. G., Romanelli, A. J., Geisler, J. G., Bhanot, S., McKay, R. A., Monia, B. P., Shutter, J. R., Lindberg, R. A., et al. (2006) · Diabetes · doi:10.2337/db05-0705 · Cited by 177 · see citing works
Activated FOXO-mediated insulin resistance is blocked by reduction of TOR activity
Luong, N., Davies, C. R., Wessells, R. J., Graham, S. M., King, M. T., Veech, R. L., Bodmer, R., & Oldham, S. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.05.013 · Cited by 171 · see citing works
Insulin action in the brain contributes to glucose lowering during insulin treatment of diabetes
Gelling, R. W., Morton, G. J., Morrison, C. D., Niswender, K. D., Myers, M. G., Rhodes, C. J., & Schwartz, M. W. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2005.11.013 · Cited by 169 · see citing works
Nasrin, N., Ogg, S., Cahill, C. M., Biggs, W., Nui, S., Dore, J., Calvo, D., Shi, Y., Ruvkun, G., & Alexander-Bridges, M. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.190326997 · Cited by 165 · see citing works
Creemers, E. E., Sutherland, L. B., McAnally, J., Richardson, J. A., & Olson, E. N. (2006) · Development · doi:10.1242/dev.02610 · Cited by 146 · see citing works
Nakae, J. (2006) · Journal of Clinical Investigation · doi:10.1172/jci25518 · Cited by 132 · see citing works
Self-citationRole of the forkhead protein FoxO1 in cell compensation to insulin resistance
Okamoto, H. (2006) · Journal of Clinical Investigation · doi:10.1172/jci24967 · Cited by 125 · see citing works
Insulin-induced phosphorylation on FKHR (Foxo1) targets to proteosomal degradation
Matsuzaki, H. (2003) · Medical Entomology and Zoology · Cited by 122 · see citing works
Okamoto, H., Obici, S., Accili, D., & Rossetti, L. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23096 · Cited by 121 · see citing works
Negative regulation of forkhead transcription factor AFX (Foxo4) by CBP-induced acetylation
Fukuoka, M., Daitoku, H., Hatta, M., Matsuzaki, H., Umemura, S., & Fukamizu, A. (2003) · International Journal of Molecular Medicine · doi:10.3892/ijmm.12.4.503 · Cited by 120 · see citing works
Insulin Regulation of PEPCK Gene Expression: A Model for Rapid and Reversible Modulation
Quinn, P. G., & Yeagley, D. (2005) · Current Drug Targets - Immune Endocrine & Metabolic Disorders · doi:10.2174/156800805774912962 · Cited by 113 · see citing works
Drosophila Melted Modulates FOXO and TOR Activity
Teleman, A. A., Chen, Y., & Cohen, S. M. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.07.004 · Cited by 113 · see citing works
Accili, D., & Taylor, S. I. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.11.4708 · Cited by 91 · see citing works
Jialal, I., Crettaz, M., HACHIYA, H. L., Kahn, C. R., Moses, A. C., Buzney, S. M., & King, G. L. (1985) · Endocrinology · doi:10.1210/endo-117-3-1222 · Cited by 90 · see citing works
Skp2 Controls Adipocyte Proliferation during the Development of Obesity
Sakai, T., Sakaue, H., Nakamura, T., Okada, M., Matsuki, Y., Watanabe, E., Hiramatsu, R., Nakayama, K., Nakayama, K., & Kasuga, M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m608144200 · Cited by 80 · see citing works
Cao, Y., Kamioka, Y., Yokoi, N., Kobayashi, T., Hino, O., Onodera, M., Mochizuki, N., & Nakae, J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m608116200 · Cited by 59 · see citing works
Self-citationSuzuki, R., Tobe, K., Aoyama, M., Inoue, A., Sakamoto, K. Q., Yamauchi, T., Kamon, J., Kubota, N., Terauchi, Y., Yoshimatsu, H., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311956200 · Cited by 59 · see citing works
Cinti, S., Eberbach, S., Castellucci, M., & Accili, D. (1998) · Diabetologia · doi:10.1007/s001250050886 · Cited by 44 · see citing works
Nuclear Forkhead Box O1 Controls and Integrates Key Signaling Pathways in Hepatocytes
Naïmi, M., Gautier, N., Chaussade, C., Valverde, Á. M., Accili, D., & OBBERGHEN, E. V. (2007) · Endocrinology · doi:10.1210/en.2006-1411 · Cited by 41 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Kamura, T., Hara, T., Kotoshiba, S., Yada, M., Ishida, N., Imaki, H., Hatakeyama, S., Nakayama, K. and Nakayama, K.I. (2003) Degradation of p57Kip2 mediated by SCFSkp2-depen- dent ubiquitylation. Proc. Natl. Acad. Sci. USA 100, 10231- 10236.
Cited by
Sorted by citations
PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer
Glaviano, A., Foo, A. S. C., Lam, H. Y., Yap, K. C. H., Jacot, W., Jones, R. H., Eng, H., Nair, M. G., Makvandi, P., Geoerger, B., et al. (2023) · Molecular Cancer · doi:10.1186/s12943-023-01827-6 · Cited by 2,138 · see citing works
MicroRNAs in metabolism and metabolic disorders
Rottiers, V., & Näär, A. M. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3313 · Cited by 1,156 · see citing works
Dietary factors and low-grade inflammation in relation to overweight and obesity
Calder, P. C., Ahluwalia, N., Brouns, F., Buetler, T., Clement, K., Cunningham, K., Esposito, K., Jönsson, L. S., Kolb, H., Lansink, M., et al. (2011) · British Journal of Nutrition · doi:10.1017/s0007114511005460 · Cited by 1,098 · see citing works
Salminen, A., Hyttinen, J. M. T., & Kaarniranta, K. (2011) · Journal of Molecular Medicine · doi:10.1007/s00109-011-0748-0 · Cited by 866 · see citing works
AMP-Activated Protein Kinase (AMPK) Controls the Aging Process via an Integrated Signaling Network
Salminen, A., & Kaarniranta, K. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2011.12.005 · Cited by 860 · see citing works
Redox regulation of FoxO transcription factors
Klotz, L.-O., Sánchez-Ramos, C., Prieto-Arroyo, I., Urbánek, P., Steinbrenner, H., & Monsalve, M. (2015) · Redox Biology · doi:10.1016/j.redox.2015.06.019 · Cited by 747 · see citing works
The cell cycle is a redox cycle: Linking phase-specific targets to cell fate
Burhans, W. C., & Heintz, N. H. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.05.026 · Cited by 359 · see citing works
Role of oxidative stress and antioxidants in daily nutrition and human health
Bjørklund, G., & Chirumbolo, S. (2016) · Nutrition · doi:10.1016/j.nut.2016.07.018 · Cited by 241 · see citing works
Lee, J. C., Espéli, M., Anderson, C. A., Linterman, M. A., Pocock, J., Williams, N. J., Roberts, R. L., Viatte, S., Fu, B., Peshu, N. M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.08.034 · Cited by 226 · see citing works
Sex Differences in Muscle Wasting
Anderson, L. J., Liu, H. M., & Garcia, J. M. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-70178-3_9 · Cited by 222 · see citing works
Jitrapakdee, S. (2011) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2011.10.001 · Cited by 189 · see citing works
Targeting Forkhead Box O1 from the Concept to Metabolic Diseases: Lessons from Mouse Models
Cheng, Z., & White, M. F. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3370 · Cited by 194 · see citing works
Regulation of neuron mitochondrial biogenesis and relevance to brain health
Onyango, I. G., Lu, J., Rodova, M., Lezi, E., Crafter, A. B., & Swerdlow, R. H. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.07.014 · Cited by 188 · see citing works
The evolutionary benefit of insulin resistance
Soeters, M. R., & Soeters, P. B. (2012) · Clinical Nutrition · doi:10.1016/j.clnu.2012.05.011 · Cited by 176 · see citing works
Role of mitochondrial homeostasis and dynamics in Alzheimer's disease
Selfridge, J. E., E, L., Lu, J., & Swerdlow, R. H. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.057 · Cited by 175 · see citing works
Potential role of F ox O 1 and m TORC 1 in the pathogenesis of W estern diet‐induced acne
Melnik, B. C., & Zouboulis, C. C. (2013) · Experimental Dermatology · doi:10.1111/exd.12142 · Cited by 163 · see citing works
Calorie restriction and the exercise of chromatinPreprint
Vaquero, A., & Reinberg, D. (2009) · Genes & Development · doi:10.1101/gad.1807009 · Cited by 154 · see citing works
Linking Alzheimer's disease to insulin resistance: the FoxO response to oxidative stress
Manolopoulos, K. N., Klotz, L.-O., Korsten, P., Bornstein, S. R., & Barthel, A. (2010) · Molecular Psychiatry · doi:10.1038/mp.2010.17 · Cited by 150 · see citing works
Dysregulated FOXO transcription factors in articular cartilage in aging and osteoarthritis
Akasaki, Y., Hasegawa, A., Saito, M., Asahara, H., Iwamoto, Y., & Lotz, M. (2013) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2013.11.004 · Cited by 140 · see citing works
The Relationship of Redox With Hallmarks of Cancer: The Importance of Homeostasis and Context
Xing, F., Hu, Q., Qin, Y., Xu, J., Zhang, B., Yu, X., & Wang, W. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.862743 · Cited by 136 · see citing works
Glucose metabolism in mammalian cell culture: new insights for tweaking vintage pathways
Mulukutla, B. C., Khan, S., Lange, A., & Hu, W.-S. (2010) · Trends in biotechnology · doi:10.1016/j.tibtech.2010.06.005 · Cited by 132 · see citing works
Regulation of triglyceride metabolism by glucocorticoid receptor
Wang, J.-C., Gray, N. E., Kuo, T., & Harris, C. A. (2012) · Cell & Bioscience · doi:10.1186/2045-3701-2-19 · Cited by 122 · see citing works
Fenofibrate Improves Renal Lipotoxicity through Activation of AMPK-PGC-1α in db/db Mice
Hong, Y. A., Lim, J. H., Kim, M. Y., Kim, T. W., Kim, Y., Yang, K. S., Park, H. S., Choi, S. R., Chung, S., Kim, H. W., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096147 · Cited by 118 · see citing works
Frijters, R., Fleuren, W., Toonen, E. J. M., Tuckermann, J. P., Reichardt, H. M., van der Maaden, H., van Elsas, A., van Lierop, M.-J., Dokter, W. H. A., de Vlieg, J., et al. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-359 · Cited by 104 · see citing works
Cleveland, B. M., & Weber, G. M. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00516.2009 · Cited by 102 · see citing works
Roles of microRNA-34a targeting SIRT1 in mesenchymal stem cells
Zhang, F., Cui, J., Liu, X., Lv, B., Liu, X., Xie, Z., & Yu, B. (2015) · Stem Cell Research & Therapy · doi:10.1186/s13287-015-0187-x · Cited by 98 · see citing works
Straub, R. H. (2014) · Arthritis Research & Therapy · doi:10.1186/ar4688 · Cited by 98 · see citing works
Wang, S., Liu, S., Liu, H., Wang, J., Zhou, S., Jiang, R., Bendena, W. G., & Li, S. (2010) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjq006 · Cited by 94 · see citing works
Ferguson-Stegall, L., McCleave, E. L., Ding, Z., Doerner, P. G., Wang, B., Liao, Y.-H., Kammer, L., Liu, Y., Hwang, J., Dessard, B. M., et al. (2011) · Journal of Strength and Conditioning Research · doi:10.1519/jsc.0b013e318212db21 · Cited by 93 · see citing works
Frontier of Epilepsy Research - mTOR signaling pathway
Cho, C. (2011) · Experimental & Molecular Medicine · doi:10.3858/emm.2011.43.5.032 · Cited by 92 · see citing works
Baicalein improves glucose metabolism in insulin resistant HepG2 cells
Yang, Z., Huang, W., Zhang, J., Xie, M., & Wang, X. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.04.005 · Cited by 91 · see citing works
Akt and PTEN: β-cell mass and pancreas plasticity
Elghazi, L., & Bernal‐Mizrachi, E. (2009) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2009.03.002 · Cited by 91 · see citing works
Shen, H., Wang, D., Li, L., Yang, S., Chen, X., Zhou, S., Zhong, S., Zhao, J., & Tang, J. (2016) · Gene · doi:10.1016/j.gene.2016.10.016 · Cited by 90 · see citing works
Molecular mechanisms of FOXO1 in adipocyte differentiation
Chen, J., Lü, Y., Tian, M., & Huang, Q. (2019) · Journal of Molecular Endocrinology · doi:10.1530/jme-18-0178 · Cited by 89 · see citing works
Haselton, A. T., Sharmin, E., Schrader, J., Sah, M., Poon, P. C., & Fridell, Y.-W. C. (2010) · Cell Cycle · doi:10.4161/cc.9.15.12458 · Cited by 88 · see citing works
Palian, B. M., Rohira, A. D., Johnson, S. A. S., He, L., Zheng, N., Dubeau, L., Stiles, B. L., & Johnson, D. L. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004789 · Cited by 87 · see citing works
Calcium Signaling in Liver Injury and Regeneration
Oliva‐Vilarnau, N., Hankeová, S., Vorrink, S. U., Mkrtchian, S., Andersson, E. R., & Lauschke, V. M. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00192 · Cited by 84 · see citing works
Xia, W., Zhang, F., Xie, C., Jiang, M., & Hou, M. (2015) · Stem Cell Research & Therapy · doi:10.1186/s13287-015-0076-3 · Cited by 85 · see citing works
Chung, H. W., Lim, J. H., Kim, M. Y., Shin, S. J., Chung, S., Choi, B. S., Kim, H. W., Kim, Y., Park, C. W., & Chang, Y. S. (2011) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfr613 · Cited by 82 · see citing works
Abadi, A. J., Zarrabi, A., Gholami, M. H., Mirzaei, S., Hashemi, F., Zabolian, A., Entezari, M., Hushmandi, K., Ashrafizadeh, M., Khan, H. Z., et al. (2021) · Biomolecules · doi:10.3390/biom11020304 · Cited by 79 · see citing works
Pattappa, G., Johnstone, B., Zellner, J., Docheva, D., & Angele, P. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030484 · Cited by 79 · see citing works
Insulin resistance and fuel homeostasis: the role of AMP‐activated protein kinase
Hegarty, B. D., Turner, N. A., Cooney, G. J., & Kraegen, E. W. (2009) · Acta Physiologica · doi:10.1111/j.1748-1716.2009.01968.x · Cited by 77 · see citing works
Cao, R., Cronk, Z. X., Zha, W., Sun, L., Wang, X., Fang, Y., Studer, E. J., Zhou, H., Pandak, W. M., Dent, P., et al. (2010) · Journal of Lipid Research · doi:10.1194/jlr.m004929 · Cited by 74 · see citing works
Silymarin Suppresses Cellular Inflammation By Inducing Reparative Stress Signaling
Lovelace, E. S., Wagoner, J., MacDonald, J., Bammler, T. K., Bruckner, J. J., Brownell, J., Beyer, R. P., Zink, E., Kim, Y., Kyle, J. E., et al. (2015) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5b00288 · Cited by 70 · see citing works
Melnik, B. C. (2011) · Dermato-Endocrinology · doi:10.4161/derm.15331 · Cited by 92 · see citing works
Concise Review: Chronic Myeloid Leukemia: Stem Cell Niche and Response to Pharmacologic Treatment
Arrigoni, E., Re, M. D., Galimberti, S., Restante, G., Rofi, E., Crucitta, S., Baratè, C., Petrini, M., Danesi, R., & Paolo, A. D. (2018) · Stem Cells Translational Medicine · doi:10.1002/sctm.17-0175 · Cited by 69 · see citing works
Nonhuman Primate Calorie Restriction
Colman, R. J., & Anderson, R. M. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3224 · Cited by 68 · see citing works
Functional crosstalk among oxidative stress and O-GlcNAc signaling pathways
Chen, P., Chi, J., & Boyce, M. (2018) · Glycobiology · doi:10.1093/glycob/cwy027 · Cited by 67 · see citing works
The cathepsin L gene is a direct target of FOXO1 in skeletal muscle
Yamazaki, Y., Kamei, Y., Sugita, S., Akaike, F., Kanai, S., Miura, S., Hirata, Y., Troen, B. R., Kitamura, T., Nishino, I., et al. (2010) · Biochemical Journal · doi:10.1042/bj20091346 · Cited by 63 · see citing works
Isotretinoin and FoxO1: A scientific hypothesis.
Melnik, B. C. (2011) · Europe PMC (PubMed Central) · doi:10.4161/derm.3.3.15331 · Cited by 62 · see citing works
Yi, G., Shen, M., Yuan, J., Sun, C., Duan, Z., Qu, L., Dou, T., Ma, M., Lü, J., Guo, J., et al. (2015) · BMC Genomics · doi:10.1186/s12864-015-1945-y · Cited by 61 · see citing works
Tissue-Specific Metabolic Regulation of FOXO-Binding Protein: FOXO Does Not Act Alone
Kodani, N., & Nakae, J. (2020) · Cells · doi:10.3390/cells9030702 · Cited by 60 · see citing works
Self-citationCandidate mechanisms accounting for effects of physical activity on breast carcinogenesis
Thompson, H. J., Jiang, W., & Zhu, Z. (2009) · IUBMB Life · doi:10.1002/iub.233 · Cited by 59 · see citing works
Integrating Opposing Signals Toward Forkhead Box O
van den Berg, M. C. W., & Burgering, B. M. T. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3415 · Cited by 57 · see citing works
Villegas-Aguilar, M. D. C., Fernández‐Ochoa, Á., Cádiz‐Gurrea, M. D. L. L., Pimentel-Moral, S., Lozano‐Sánchez, J., Arraéz-Román, D., & Segura‐Carretero, A. (2020) · Molecules · doi:10.3390/molecules25030596 · Cited by 59 · see citing works
Role of Reductive versus Oxidative Stress in Tumor Progression and Anticancer Drug Resistance
Chun, K., Kim, D., & Surh, Y. (2021) · Cells · doi:10.3390/cells10040758 · Cited by 55 · see citing works
Resistance Exercise, Skeletal Muscle FOXO3A, and 85-Year-Old Women
Williamson, D. L., Raue, U., Slivka, D. R., & Trappe, S. W. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq005 · Cited by 54 · see citing works
Control of hepatic glucose metabolism by islet and brain
Rojas, J. M., & Schwartz, M. W. (2014) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12332 · Cited by 52 · see citing works
The FOXO’s Advantages of Being a Family: Considerations on Function and Evolution
Schmitt-Ney, M. (2020) · Cells · doi:10.3390/cells9030787 · Cited by 52 · see citing works
Longevity Genes: Insights from Calorie Restriction and Genetic Longevity Models
Shimokawa, I., Chiba, T., Yamaza, H., & Komatsu, T. (2008) · Molecules and Cells · doi:10.1016/s1016-8478(23)14018-0 · Cited by 50 · see citing works
Maissan, P., Mooij, E., & Barberis, M. (2021) · Biology · doi:10.3390/biology10030194 · Cited by 50 · see citing works
Docosahexaenoic acid suppresses the expression of FoxO and its target genes
Chen, Y.-J., Chen, C.-C., Li, T., Wang, P.-H., Liu, L.-R., Chang, F.-Y., Wang, Y.-C., Yu, Y., Lin, S., Mersmann, H. J., et al. (2012) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.11.003 · Cited by 48 · see citing works
Kohan, K., Carvajal, R., Gabler, F., Vantman, D., Romero, C., & Vega, M. (2010) · Reproduction · doi:10.1530/rep-10-0056 · Cited by 49 · see citing works
Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease
Reich, N., & Hölscher, C. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.614828 · Cited by 48 · see citing works
“As such, the function of variousmitochondrial master modulators, including AMPK and PGC1α, is disturbed in AD and PD.”
BackgroundInfluentialMitochondrial function and diabetes: consequences for skeletal and cardiac muscle metabolism
Schrauwen-Hinderling, V. B., Kooi, M. E., & Schrauwen, P. (2016) · Antioxidants & Redox Signaling · doi:10.1089/ars.2015.6291 · Cited by 47 · see citing works
PPARα agonist, fenofibrate, ameliorates age-related renal injury
Kim, E. N., Lim, J. H., Kim, M. Y., Kim, H. W., Park, C. W., Chang, Y. S., & Choi, B. S. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.04.021 · Cited by 43 · see citing works
Kuo, S., Liu, S., Huang, Y., Tsai, C., Fong, Y., Hsu, H., & Tang, C. (2019) · Aging · doi:10.18632/aging.102038 · Cited by 43 · see citing works
Tomlinson, J. J., Boudreau, A., Wu, D., Salem, H. A., Carrigan, A., Gagnon, A., Mears, A. J., Sorisky, A., Atlas, E., & Haché, R. J. G. (2009) · Molecular Endocrinology · doi:10.1210/me.2009-0091 · Cited by 43 · see citing works
Zhang, X., Jiang, L., & Liu, H. (2021) · Drug Design Development and Therapy · doi:10.2147/dddt.s305016 · Cited by 42 · see citing works
Fox tales: Regulation of gonadotropin gene expression by forkhead transcription factors
Thackray, V. G. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.09.034 · Cited by 39 · see citing works
The forkhead box O3 (FOXO3): a key player in the regulation of ischemia and reperfusion injury
Omorou, M., Huang, Y., Gao, M., Mu, C., Xu, W., Han, Y., & Xu, H. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04755-2 · Cited by 40 · see citing works
Gut-brain mechanisms controlling glucose homeostasis
Scarlett, J. M., & Schwartz, M. W. (2015) · F1000Prime Reports · doi:10.12703/p7-12 · Cited by 38 · see citing works
Komatsu, T., Park, S., Hayashi, H., Mori, R., Yamaza, H., & Shimokawa, I. (2019) · Nutrients · doi:10.3390/nu11123068 · Cited by 38 · see citing works
Horikawa, M., & Sakamoto, K. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.03.004 · Cited by 38 · see citing works
H. Swerdlow, R. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211798072535 · Cited by 35 · see citing works
Hepp, P., Hutter, S., Knabl, J., Hofmann, S., Kühn, C., Mahner, S., & Jeschke, U. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19124061 · Cited by 34 · see citing works
Novel repressor regulates insulin sensitivity through interaction with Foxo1
Nakae, J., Cao, Y., Hakuno, F., Takemori, H., Kawano, Y., Sekioka, R., Abe, T., Kiyonari, H., Tanaka, T., Sakai, J., et al. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.97 · Cited by 34 · see citing works
Self-citationLuo, K., Huang, W., Qiao, L., Zhang, X., Yan, D., Ning, Z.-Y., Ma, C., Dang, H., Wang, D., Guo, H., et al. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.11.017 · Cited by 33 · see citing works
Rajan, M. R., Nyman, E., Kjølhede, P., Cedersund, G., & Strålfors, P. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.715763 · Cited by 32 · see citing works
Muscle development and obesity
Maltin, C. A. (2008) · Organogenesis · doi:10.4161/org.4.3.6312 · Cited by 32 · see citing works
The B55α-containing PP2A holoenzyme dephosphorylates FOXO1 in islet β-cells under oxidative stress
Yan, L., Guo, S., Brault, M. A., Harmon, J. S., Robertson, R. P., Hamid, R., Stein, R. W., & Yang, E. (2012) · Biochemical Journal · doi:10.1042/bj20111606 · Cited by 31 · see citing works
Kan, H., Huang, Y., Li, X., Liu, D., Chen, J., & Shu, M. (2016) · Oncotarget · doi:10.18632/oncotarget.7425 · Cited by 31 · see citing works
The role of redox environment in neurogenic development
Ostrakhovitch, E. A., & Semenikhin, O. A. (2012) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2012.08.002 · Cited by 30 · see citing works
Sargent, K. M., Lu, N., Clopton, D. T., Pohlmeier, W. E., Brauer, V. M., Ferrara, N., Silversides, D. W., & Cupp, A. S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116332 · Cited by 30 · see citing works
Zhang, Y., Luo, J., Zhu, T., Zhang, X., Jin, M., Jiao, L., Meng, F., Figueiredo-Silva, C., Hong, Y., & Zhou, Q. (2022) · Aquaculture Reports · doi:10.1016/j.aqrep.2022.101088 · Cited by 29 · see citing works
Schnitzler, F., Friedrich, M., Wolf, C., Angelberger, M., Diegelmann, J., Olszak, T., Beigel, F., Tillack, C., Stallhofer, J., Göke, B., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108503 · Cited by 29 · see citing works
Mechanisms of transcription factor acetylation and consequences in hearts
Thiagarajan, D., Vedantham, S., Ananthakrishnan, R., Schmidt, A. M., & Ramasamy, R. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.08.011 · Cited by 28 · see citing works
Lu, X., Yin, D., Zhou, B., & Li, T. (2018) · International Heart Journal · doi:10.1536/ihj.17-040 · Cited by 28 · see citing works
Babaee, M., Chamani, E., Ahmadi, R., Bahreini, E., Balouchnejadmojarad, T., Nahrkhalaji, A. S., & Fallah, S. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117898 · Cited by 27 · see citing works
Szczuko, M., Zapałowska-Chwyć, M., Maciejewska, D., Drozd, A., Starczewski, A., & Stachowska, E. (2016) · Medical Hypotheses · doi:10.1016/j.mehy.2016.09.016 · Cited by 27 · see citing works
Revving the engine: PKB/AKT as a key regulator of cellular glucose metabolism
Li, X., Hu, S., Cai, Y., Liu, X., Luo, J., & Wu, T. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2023.1320964 · Cited by 25 · see citing works
Kappel, B. A., Stöhr, R., Angelis, L. D., Mavilio, M., Menghini, R., & Federici, M. (2016) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2016.04.001 · Cited by 25 · see citing works
Kajihara, T., Uchino, S., Suzuki, M., Itakura, A., Brosens, J. J., & Ishihara, O. (2009) · Medical Molecular Morphology · doi:10.1007/s00795-009-0466-7 · Cited by 25 · see citing works
Che, X., Shang, X., Weixu, Xing, M., Wei, H., Li, W., Li, Z., Teng, X., & Geng, L. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.141204 · Cited by 24 · see citing works
Shi, B., Tao, X., Betancor, M. B., Lu, J., Tocher, D. R., Meng, F., Figueiredo-Silva, C., Zhou, Q., Jiao, L., & Jin, M. (2021) · Aquatic Toxicology · doi:10.1016/j.aquatox.2021.105967 · Cited by 23 · see citing works
The FOX transcription factors regulate vascular pathology diabetes and Tregs
Yang, X. F. (2009) · Frontiers in Bioscience-Scholar · doi:10.2741/s35 · Cited by 23 · see citing works
Bednářová, A., Tomčala, A., Mochanová, M., Kodrı́k, D., & Krishnan, N. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00949 · Cited by 22 · see citing works
AMPK: A promising molecular target for combating cisplatin toxicities
Rashtchizadeh, N., Argani, H., Ghorbanihaghjo, A., Sanajou, D., Hosseini, V., Dastmalchi, S., & Ahmad, S. N. S. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.02.006 · Cited by 22 · see citing works
Raju, I., Kannan, K., & Abraham, E. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067126 · Cited by 21 · see citing works
Liang, S., Guo, J., Choi, J.-W., Shin, K.-T., Wang, H.-Y., Jo, Y.-J., Kim, N.-H., & Cui, X.-S. (2017) · Oncotarget · doi:10.18632/oncotarget.15927 · Cited by 20 · see citing works
- Authors
- Nakae, J., Oki, M., & Cao, Y.
- Affiliations
- Kobe University (JP)
- Corresponding author
- Nakae, Jun
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 2007-11-20
- Volume
- 582
- Issue
- 1
- Pages
- 54-67
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W2085299577
- Cited by
- 176
- References
- 135
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 4 · 2023: 5 · 2022: 4 · 2021: 14 · 2020: 9 · 2019: 11 · 2018: 13 · 2017: 7 · 2016: 13 · 2015: 17 · 2014: 10 · 2013: 9 · 2012: 11
- FWCI
- 0.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- FEBS Letters (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › FOXO transcription factor regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fibroblast Growth Factor Research
- Keywords
- FOXO transcription factors, forkhead transcription factor, insulin signaling, caloric restriction, starvation, hepatic glucose production, insulin secretion, dietary intake, insulin resistance, type 2 diabetes, hyperlipidemia, metabolic syndrome, glucose metabolism, lipid metabolism
- MeSH terms
- Animals, Humans, Insulin, Metabolism, Transcription Factors, Signal Transduction, Mice, Knockout, 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