The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Hepatic insulin signalling is dispensable for suppression of glucose output by insulin in vivo
Open accessAbstract
Insulin signalling and nutrient levels coordinate the metabolic response to feeding in the liver. Insulin signals in hepatocytes to activate Akt, which inhibits Foxo1 suppressing hepatic glucose production (HGP) and allowing the transition to the postprandial state. Here we provide genetic evidence that insulin regulates HGP by both direct and indirect hepatic mechanisms. Liver-specific ablation of the IR (L-Insulin Receptor KO) induces glucose intolerance, insulin resistance and prevents the appropriate transcriptional response to feeding. Liver-specific deletion of Foxo1 (L-IRFoxo1DKO) rescues glucose tolerance and allows for normal suppression of HGP and gluconeogenic gene expression in response to insulin, despite lack of autonomous liver insulin signalling. These data indicate that in the absence of Foxo1, insulin signals via an intermediary extrahepatic tissue to regulate liver glucose production. Importantly, a hepatic mechanism distinct from the IR–Akt–Foxo1 axis exists to regulate glucose production. Insulin and the transcription factor FoxO1 are key regulators of hepatic glucose metabolism. Here, Titchenell et al. provide evidence for the existence of an insulin-dependent extrahepatic pathway that is fully capable of regulating hepatic glucose production in the absence of hepatic FoxO1.
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
“Intact hepatic insulin signaling is, however, dispensable for the postprandial repression of hepatic glucose production in the absence of hepatic FoxO1 32, 33, highlighting the importance of hypothalamic insulin signaling in the control of liver glucose metabolism 34.”
From Inter‐organ communication: a gatekeeper for metabolic health (2019) · cites this paper as [33]
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
Insulin signalling and the regulation of glucose and lipid metabolism
Saltiel, A. R., & Kahn, C. R. (2001) · Nature · doi:10.1038/414799a · Cited by 5,326
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
Michael, M. D., Kulkarni, R. N., Postic, C., Previs, S. F., Shulman, G. I., Magnuson, M. A., & Kahn, C. R. (2000) · Molecular Cell · doi:10.1016/s1097-2765(05)00015-8 · Cited by 1,296
Brüning, J. C., Michael, M. D., Winnay, J. N., Hayashi, T., Hörsch, D., Accili, D., Goodyear, L. J., & Kahn, C. R. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80155-0 · Cited by 1,173
The CREB coactivator TORC2 is a key regulator of fasting glucose metabolism
Koo, S., Flechner, L., Qi, L., Zhang, X., Screaton, R. A., Jeffries, S., Hedrick, S. A., Xu, W., Boussouar, F., Brindle, P. K., et al. (2005) · Nature · doi:10.1038/nature03967 · Cited by 1,026
Menon, S., Dibble, C. C., Talbott, G., Hoxhaj, G., Valvezan, A. J., Takahashi, H., Cantley, L. C., & Manning, B. D. (2014) · Cell · doi:10.1016/j.cell.2013.11.049 · Cited by 766
Li, S., Brown, M. S., & Goldstein, J. L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914798107 · Cited by 733
Insulin Action in AgRP-Expressing Neurons Is Required for Suppression of Hepatic Glucose Production
Könner, A. C., Janoschek, R., Plum, L., Jordan, S. D., Rother, E., Ma, X., Xu, C., Enriori, P., Hampel, B., Barsh, G. S., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.05.004 · Cited by 695
Yecies, J. L., Zhang, H., Menon, S., Liu, S., Yecies, D. W., Lipovsky, A. I., Görgün, C. Z., Kwiatkowski, D. J., Hotamışlıgil, G. S., Lee, C., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.06.002 · Cited by 685
Matsumoto, M., Pocai, A., Rossetti, L., DePinho, R. A., & Accili, D. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.08.006 · Cited by 624
Cited by
Sorted by citations
Mechanisms of Insulin Action and Insulin Resistance
Petersen, M. C., & Shulman, G. I. (2018) · Physiological Reviews · doi:10.1152/physrev.00063.2017 · Cited by 3,028
The PI3K/AKT Pathway in Obesity and Type 2 Diabetes
Huang, X., Liu, G., Guo, J., & Su, Z. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.27173 · Cited by 1,673
“Additionally, those mice still maintained the normal postprandial state, even in the absence of canonical liver insulin signalling [85, 87].”
BackgroundResultThe integrative biology of type 2 diabetes
Roden, M., & Shulman, G. I. (2019) · Nature · doi:10.1038/s41586-019-1797-8 · Cited by 1,167
Regulation of hepatic glucose metabolism in health and disease
Petersen, M. C., Vatner, D. F., & Shulman, G. I. (2017) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2017.80 · Cited by 1,159
Tilg, H., Moschen, A. R., & Roden, M. (2017) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2016.147 · Cited by 1,002
Jang, C., Oh, S. F., Wada, S., Rowe, G. C., Liu, L., Chan, M. C., Rhee, J., Hoshino, A., Kim, B., Ibrahim, A., et al. (2016) · Nature Medicine · doi:10.1038/nm.4057 · Cited by 604
Self-citationInsulin regulation of gluconeogenesis
Hatting, M., Tavares, C. D. J., Sharabi, K., Rines, A. K., & Puigserver, P. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13435 · Cited by 625
Dietary fructose feeds hepatic lipogenesis via microbiota-derived acetate
Zhao, S., Jang, C., Liu, J., Uehara, K., Gilbert, M., Izzo, L., Zeng, X., Trefely, S., Fernandez, S., Carrer, A., et al. (2020) · Nature · doi:10.1038/s41586-020-2101-7 · Cited by 553
Self-citationRole of Insulin Resistance in MAFLD
Sakurai, Y., Kubota, N., Yamauchi, T., & Kadowaki, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084156 · Cited by 448
Unraveling the Regulation of Hepatic Metabolism by Insulin
Titchenell, P. M., Lazar, M. A., & Birnbaum, M. J. (2017) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2017.03.003 · Cited by 457
Self-citationFox transcription factors: from development to disease
Golson, M. L., & Kaestner, K. H. (2016) · Development · doi:10.1242/dev.112672 · Cited by 406
Insulin Receptor Isoforms in Physiology and Disease: An Updated View
Belfiore, A., Malaguarnera, R., Vella, V., Lawrence, M. C., Sciacca, L., Frasca, F., Morrione, A., & Vigneri, R. (2017) · Endocrine Reviews · doi:10.1210/er.2017-00073 · Cited by 390
FoxO integration of insulin signaling with glucose and lipid metabolism
Lee, S., & Dong, H. H. (2017) · Journal of Endocrinology · doi:10.1530/joe-17-0002 · Cited by 365
Resolving the paradox of hepatic insulin resistance
Santoleri, D., & Titchenell, P. M. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.10.016 · Cited by 336
“These mice also fail to promote hepatic lipogenesis in response to a high carbohydrate meal.(16) Resolving what specific factors mediate insulin action on the liver to generate these paradoxical effects has become a major focus in obesity and T2DM studies and has provided many insights into the molecular mechanisms of…”
BackgroundSelf-citationBo, T., Gao, L., Yao, Z., Shao, S., Wang, X., Proud, C. G., & Zhao, J. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.04.006 · Cited by 293
Titchenell, P. M., Quinn, W. J., Lu, M., Chu, Q., Lu, W., Li, C., Chen, H., Monks, B. R., Chen, J., Rabinowitz, J. D., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.04.022 · Cited by 298
Self-citationO-Sullivan, I., Zhang, W., Wasserman, D. H., Liew, C. W., Liu, J., Paik, J., DePinho, R. A., Stolz, D. B., Kahn, C. R., Schwartz, M. W., et al. (2015) · Nature Communications · doi:10.1038/ncomms8079 · Cited by 228
Metabolic drivers of non-alcoholic fatty liver disease
Bence, K. K., & Birnbaum, M. J. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101143 · Cited by 230
Self-citationHepatic NADH reductive stress underlies common variation in metabolic traits
Goodman, R. P., Markhard, A. L., Shah, H., Sharma, R., Skinner, O. S., Clish, C. B., Deik, A., Patgiri, A., Hsu, Y.-H. H., Masia, R., et al. (2020) · Nature · doi:10.1038/s41586-020-2337-2 · Cited by 211
Brain insulin signalling in metabolic homeostasis and disease
Scherer, T., Sakamoto, K., & Buettner, C. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00498-x · Cited by 205
Parlati, L., Régnier, M., Guillou, H., & Postic, C. (2021) · JHEP Reports · doi:10.1016/j.jhepr.2021.100346 · Cited by 201
Ins and outs of the TCA cycle: the central role of anaplerosis
Inigo, M., Deja, S., & Burgess, S. C. (2021) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-120420-025558 · Cited by 189
Inter‐organ communication: a gatekeeper for metabolic health
Castillo‐Armengol, J., Fajas, L., & Lopez‐Mejia, I. C. (2019) · The EMBO Reports · doi:10.15252/embr.201947903 · Cited by 178
Adipose tissue mTORC2 regulates ChREBP-driven de novo lipogenesis and hepatic glucose metabolism
Tang, Y., Wallace, M., Sánchez-Gurmaches, J., Hsiao, W., Li, H., Lee, P. L., Vernia, S., Metallo, C. M., & Guertin, D. A. (2016) · Nature Communications · doi:10.1038/ncomms11365 · Cited by 188
Kubota, T., Kubota, N., & Kadowaki, T. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.03.004 · Cited by 174
Ginsenoside Rg1 Inhibits Glucagon-Induced Hepatic Gluconeogenesis through Akt-FoxO1 Interaction
Liu, Q., Zhang, F.-G., Zhang, W., Pan, A., Yang, Y., Liu, J., Li, P., Liu, B., & Qi, L. (2017) · Theranostics · doi:10.7150/thno.18788 · Cited by 158
Scarlett, J. M., Rojas, J. M., Matsen, M. E., Kaiyala, K. J., Stefanovski, D., Bergman, R. N., Hồng, N. T., Dorfman, M. D., Lantier, L., Wasserman, D. H., et al. (2016) · Nature Medicine · doi:10.1038/nm.4101 · Cited by 150
Obesity: Pathophysiology, monosodium glutamate-induced model and anti-obesity medicinal plants
Hernández-Bautista, R., Mahmoud, A. M., Königsberg, M., & López‐Díazguerrero, N. E. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.12.108 · Cited by 158
Long Noncoding RNA lncSHGL Recruits hnRNPA1 to Suppress Hepatic Gluconeogenesis and Lipogenesis
Wang, J., Yang, W., Chen, Z., Chen, J., Meng, Y., Feng, B., Sun, L., Dou, L., Li, J., Cui, Q., et al. (2018) · Diabetes · doi:10.2337/db17-0799 · Cited by 138
Mu, W., Cheng, X., Liu, Y., Lv, Q., Gao-lin, L., Zhang, J.-G., & Li, X. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01566 · Cited by 127
Taheri, R., Mokhtari, Y., Yousefi, A., & Bashash, D. (2024) · Cell Biology International · doi:10.1002/cbin.12189 · Cited by 116
Inactivating hepatic follistatin alleviates hyperglycemia
Tao, R., Wang, C., Stöhr, O., Qiu, W., Hu, Y., Miao, J., Dong, X. C., Leng, S., Stefater, M., Stylopoulos, N., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0048-0 · Cited by 104
Intercellular Transmission of Hepatic ER Stress in Obesity Disrupts Systemic Metabolism
Tirosh, A., Tuncman, G., Calay, E. S., RATHAUS, M., Ron, I., Tirosh, A., Yalçın, A., Lee, Y. G., Livne, R., Ron, S., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.11.009 · Cited by 106
Muscle Directs Diurnal Energy Homeostasis through a Myokine-Dependent Hormone Module in Drosophila
Zhao, X. L., & Karpac, J. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.004 · Cited by 93
Hypothalamic Control of Systemic Glucose Homeostasis: The Pancreas Connection
Pozo, M., & Claret, M. (2018) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2018.05.001 · Cited by 97
Hypothalamic Insulin Resistance in Obesity: Effects on Glucose Homeostasis
Chen, W., Balland, É., & Cowley, M. A. (2017) · Neuroendocrinology · doi:10.1159/000455865 · Cited by 101
mTORC1 stimulates phosphatidylcholine synthesis to promote triglyceride secretion
Quinn, W. J., Wan, M., Shewale, S. V., Gelfer, R., Rader, D. J., Birnbaum, M. J., & Titchenell, P. M. (2017) · Journal of Clinical Investigation · doi:10.1172/jci96036 · Cited by 96
Self-citationHepatic Dysfunction Caused by Consumption of a High-Fat Diet
Soltis, A. R., Kennedy, N. J., Xin, X., Zhou, F., Ficarro, S. B., Yap, Y. S., Matthews, B. J., Lauffenburger, D. A., White, F. M., Marto, J. A., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.059 · Cited by 100
Sphingolipid metabolism in non-alcoholic fatty liver diseases
Régnier, M., Polizzi, A., Guillou, H., & Loiseau, N. (2018) · Biochimie · doi:10.1016/j.biochi.2018.07.021 · Cited by 88
Truong, X. T., & Lee, D. H. (2025) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2025.0644 · Cited by 84
“In mice, concomitant deletion of FoxO1 in an AKT-deficient liver is not sufficient to drive DNL but restores insulin sensitivity and glucose tolerance, suggesting there are other pathways downstream of AKT that contribute to DNL [12,32].”
Zhang, W., Bu, S. Y., Mashek, M. T., O‐Sullivan, I., Sibai, Z., Khan, S. A., Ilkayeva, O., Newgard, C. B., Mashek, D. G., & Unterman, T. G. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.03.021 · Cited by 82
Physiological Suppression of Lipotoxic Liver Damage by Complementary Actions of HDAC3 and SCAP/SREBP
Papazyan, R., Sun, Z., Kim, Y. H., Titchenell, P. M., Hill, D. A., Lu, W., Damle, M., Wan, M., Zhang, Y., Briggs, E. R., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.10.012 · Cited by 80
Self-citationQi, B., Ren, D., Li, T., Niu, P., Zhang, X., Yang, X., & Xiao, J. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c02400 · Cited by 76
Acierno, C., Caturano, A., Pafundi, P. C., Nevola, R., Adinolfi, L. E., & Sasso, F. C. (2020) · Exploration of Medicine · doi:10.37349/emed.2020.00019 · Cited by 81
Metabolic Role of PTEN in Insulin Signaling and ResistancePreprint
Li, Y. Z., Cristofano, A. D., & Woo, M. (2020) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a036137 · Cited by 76
Hepatic Glucagon Receptor Signaling Enhances Insulin-Stimulated Glucose Disposal in Rodents
Kim, T., Holleman, C. L., Nason, S. R., Arble, D. M., Ottaway, N., Chabenne, J. R., Loyd, C., Kim, J., Sandoval, D. A., Drucker, D. J., et al. (2018) · Diabetes · doi:10.2337/db18-0068 · Cited by 69
LRG1 is an adipokine that mediates obesity-induced hepatosteatosis and insulin resistance
He, S., Ryu, J., Liu, J., Luo, H., Lv, Y., Langlais, P. R., Wen, J., Dong, F., Sun, Z., Xia, W., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci148545 · Cited by 71
Triglycerides in Nonalcoholic Fatty Liver Disease: Guilty Until Proven Innocent
Semova, I., & Biddinger, S. B. (2021) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2020.12.001 · Cited by 69
Kalviša, A., Siersbæk, M. S., Præstholm, S. M., Christensen, L. J. L., Nielsen, R., Stöhr, O., Vettorazzi, S., Tuckermann, J. P., White, M. F., Mandrup, S., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2006249 · Cited by 63
The role of adipose tissue dysfunction in hepatic insulin resistance and T2D
Sancar, G., & Birkenfeld, A. L. (2024) · Journal of Endocrinology · doi:10.1530/joe-24-0115 · Cited by 69
FoxO1 antagonist suppresses autophagy and lipid droplet growth in adipocytes
Liu, L., Zheng, L., Zou, P., Brooke, J., Smith, C., Long, Y. C., Almeida, F. A., Liu, D., & Cheng, Z. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1192732 · Cited by 60
The adipocyte supersystem of insulin and cAMP signaling
Guilherme, A., Rowland, L. A., Wang, H., & Czech, M. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.07.009 · Cited by 59
Edgerton, D. S., Scott, M. F., Farmer, B., Williams, P. E., Madsen, P., Kjeldsen, T., Brand, C. L., Fledelius, C., Nishimura, E., & Cherrington, A. D. (2019) · JCI Insight · doi:10.1172/jci.insight.126974 · Cited by 61
Duca, F. A., Bauer, P. V., Hamr, S. C., & Lam, T. K. T. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.003 · Cited by 62
Wu, F., Shao, Q., Xia, Q., Hu, M., Zhao, Y. Q., Wang, D., Fang, K., Xu, L., Zou, X., Chen, Z., et al. (2021) · Phytomedicine · doi:10.1016/j.phymed.2021.153487 · Cited by 53
Cady, G., Landeryou, T., Garratt, M., Kopchick, J. J., Qi, N., García-Galiano, D., Elias, C. F., Myers, M. G., Miller, R. A., Sandoval, D. A., et al. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.03.001 · Cited by 52
Liver and insulin resistance: New wine in old bottle!!!
Patel, B. M., & Goyal, R. K. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.172657 · Cited by 51
Insulin Regulation of Hepatic Lipid Homeostasis
Uehara, K., Santoleri, D., Whitlock, A. E. G., & Titchenell, P. M. (2023) · Comprehensive Physiology · doi:10.1002/cphy.c220015 · Cited by 49
Self-citationFerdous, S.-E., & Ferrell, J. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168731 · Cited by 56
The adipokine sFRP4 induces insulin resistance and lipogenesis in the liver
Hörbelt, T., Knebel, B., Fahlbusch, P., Barbosa, D., de Wiza, D. H., de Velde, F. V., Nieuwenhove, Y. V., Lapauw, B., Thoresen, G. H., Al‐Hasani, H., et al. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2019.07.008 · Cited by 47
Gröger, M., Matsuo, K., Arash, E. H., Pereira, A., Guillou, D. L., Pino, C., Telles-Silva, K. A., Maher, J. J., Hsiao, E. C., & Willenbring, H. (2023) · Nature Communications · doi:10.1038/s41467-023-39311-w · Cited by 47
MicroRNA-21 regulates hepatic glucose metabolism by targeting FOXO1
Luo, A., Yan, H., Liang, J., Du, C., Zhao, X., Sun, L., & Chen, Y. (2017) · Gene · doi:10.1016/j.gene.2017.06.024 · Cited by 44
Du, Q., Zhang, S., Li, A., Mohammad, I. S., Liu, B., & Li, Y. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00015 · Cited by 45
Regulation of Glucose Production in the Pathogenesis of Type 2 Diabetes
Sargsyan, A., & Herman, M. A. (2019) · Current Diabetes Reports · doi:10.1007/s11892-019-1195-5 · Cited by 42
Niacin fine‐tunes energy homeostasis through canonical GPR109A signaling
Ye, L., Cao, Z., Lai, X., Wang, W., Guo, Z., Yan, L., Wang, Y., Shi, Y., & Zhou, N. (2018) · The FASEB Journal · doi:10.1096/fj.201801951r · Cited by 38
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase
Leiter, S. M., Parker, V., Welters, A., Knox, R. G., Rocha, N., Clark, G. R., Payne, F., Lotta, L. A., Harris, J. R., Guerrero-Fernández, J., et al. (2017) · European Journal of Endocrinology · doi:10.1530/eje-17-0132 · Cited by 38
Hepatocyte ABCA1 Deletion Impairs Liver Insulin Signaling and Lipogenesis
Key, C.-C. C., Liu, M., Kurtz, C. L., Chung, S., Boudyguina, E. Y., Dinh, T. A., Bashore, A. C., Phelan, P. E., Freedman, B. I., Osborne, T. F., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.032 · Cited by 40
Dittmann, A., Kennedy, N. J., Soltero, N. L., Morshed, N., Mana, M., Yilmaz, Ö. H., Davis, R. J., & White, F. M. (2019) · Molecular Systems Biology · doi:10.15252/msb.20198849 · Cited by 34
Goldsworthy, M., Bai, Y., Li, C.-M., Ge, H., Lamas, E., Hilton, H., Esapa, C. T., Baker, D., Baron, W., Juan, T., et al. (2016) · Diabetes · doi:10.2337/db15-1276 · Cited by 35
Elumalai, A., & Jain, S. K. (2017) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2017.07.016 · Cited by 31
Avilkina, V., Chauveau, C., & Mhenni, O. G. (2021) · Bone · doi:10.1016/j.bone.2021.116232 · Cited by 33
Deconstructing the Role of PKC Epsilon in Glucose Homeostasis
Schmitz‐Peiffer, C. (2020) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2020.01.016 · Cited by 30
Lu, J., Tao, X., Li, M., Zhang, X., Zhou, Q., Luo, J., Zhu, T., Jiao, L., & Jin, M. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.739910 · Cited by 29
Ling, A. V., Gearing, M. E., Semova, I., Shin, D., Clements, R. L., Lai, Z. W., & Biddinger, S. B. (2017) · Endocrinology · doi:10.1210/en.2017-00870 · Cited by 30
Wang, L., Yu, J., Zhou, Q., Wang, X., Mukhanova, M., Du, W. J., Sun, L., Pajvani, U. B., & Accili, D. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.11.013 · Cited by 28
Regulation of Hepatic Glucose Metabolism by FoxO Proteins, an Integrated Approach
Unterman, T. G. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.10.005 · Cited by 28
Loss of FOXO transcription factors in the liver mitigates stress-induced hyperglycemia
Whitlock, A. E. G., Sostre‐Colón, J., Gavin, M. J., Martin, N. D., Baur, J. A., Sims, C. A., & Titchenell, P. M. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101246 · Cited by 29
Self-citationSostre‐Colón, J., Uehara, K., Whitlock, A. E. G., Gavin, M. J., Ishibashi, J., Potthoff, M. J., Seale, P., & Titchenell, P. M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109128 · Cited by 26
Self-citationInsulin–Dendrimer Nanocomplex for Multi‐Day Glucose‐Responsive Therapy in Mice and Swine
Xian, S., Xiang, Y., Liu, D., Fan, B., Mitrová, K., Ollier, R. C., Su, B., Alloosh, M. A., Jiráček, J., Sturek, M. S., et al. (2023) · Advanced Materials · doi:10.1002/adma.202308965 · Cited by 26
Varghese, J., James, J., Vaulont, S., McKie, A. T., & Jacob, M. (2018) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2018.05.022 · Cited by 25
Xie, X., Yan, D., Li, H., Zhu, Q., Li, J., Fang, Y., Cheung, C. W., Irwin, M. G., Xia, Z., & Lian, Q. (2018) · Journal of Diabetes Research · doi:10.1155/2018/6254340 · Cited by 27
Crosstalk between bone and other organs
Yuan, W., & Song, C. (2022) · Medical Review · doi:10.1515/mr-2022-0018 · Cited by 27
Corbit, K. C., Camporez, J. P., Edmunds, L. R., Tran, J. L., Vera, N. B., Erion, D. M., Deo, R. C., Perry, R. J., Shulman, G. I., Jurczak, M. J., et al. (2017) · Diabetes · doi:10.2337/db17-0524 · Cited by 20
Caracciolo, V., Young, J., Gonzales, D. M., Ni, Y., Flowers, S. J., Summer, R. S., Waldman, S. A., Kim, J. K., Jung, D. Y., Noh, H. L., et al. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00224.2017 · Cited by 20
Merry, T. L., Hedges, C. P., Masson, S. W. C., Laube, B., Pöhlmann, D., Wueest, S., Walsh, M. E., Arnold, M., Langhans, W., Konrad, D., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15623-z · Cited by 20
Jiang, Y., Zhu, H., Chen, Z., Yu, Y., Guo, X., Chen, Y., Yang, M., Chen, B.-W., Sagnelli, M., Xu, D. Q., et al. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.844707 · Cited by 21
An integrative transcriptional logic model of hepatic insulin resistance
Kitamoto, T., Kuo, T., Okabe, A., Kaneda, A., & Accili, D. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2102222118 · Cited by 20
Insulin Resistance in Type 2 Diabetes
Roden, M., Petersen, K. F., & Shulman, G. I. (2016) · Wiley eBooks · doi:10.1002/9781118924853.ch13 · Cited by 20
Modulation of Glucose Production by Central Insulin Requires IGF-1 Receptors in AgRP Neurons
Quipildor, G. F., Mao, K., Beltran, P. J., Barzilai, N., & Huffman, D. M. (2021) · Diabetes · doi:10.2337/db21-0028 · Cited by 19
IPMK modulates hepatic glucose production and insulin signaling
Jung, I., Anokye‐Danso, F., Jin, S., Ahima, R. S., & Kim, S. F. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30827 · Cited by 19
FoxO1: mute for a tuned metabolism?
Cheng, Z. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.06.006 · Cited by 19
Kumar, K. K., Aburawi, E. H., Ljubisavljević, M., Leow, M. K., Xu, F., Ansari, S. A., & Emerald, B. S. (2024) · Clinical Epigenetics · doi:10.1186/s13148-024-01692-0 · Cited by 22
Regulation of Hepatic Metabolism, Recent Advances, and Future Perspectives
Sharabi, K., Tavares, C. D. J., & Puigserver, P. (2019) · Current Diabetes Reports · doi:10.1007/s11892-019-1224-4 · Cited by 21
Wang, Y., Fan, M., Qian, H., Ying, H., Li, Y., & Wang, L. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2183382 · Cited by 20
Role of AMPD2 in impaired glucose tolerance induced by high fructose diet
Hudoyo, A. W., Hirase, T., Tandelilin, A., Honda, M., Shirai, M., Cheng, J., Morisaki, H., & Morisaki, T. (2017) · Molecular Genetics and Metabolism Reports · doi:10.1016/j.ymgmr.2017.07.006 · Cited by 18
Zhang, J., Wang, X., Huajun, J., Yang, F., Du, Y., Wang, L., & Hong, B. (2022) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2022.03.007 · Cited by 17
Liebmann, M., Pfeifer, M. A., Grupe, K., & Scherneck, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126693 · Cited by 18
FOXO: a key target in regulating aging and age-related diseases
Wang, W., Zhu, H., Jiang, Q., Shi, Y., & Wang, X. (2026) · Biogerontology · doi:10.1007/s10522-025-10380-2 · Cited by 18
Passaro, A., Sanz, J. M., Naumovski, N., & Sergi, D. (2024) · Advances in Redox Research · doi:10.1016/j.arres.2024.100100 · Cited by 17
Okuyama, T., Shirakawa, J., Tajima, K., Ino, Y., Vethe, H., Togashi, Y., Kyohara, M., Inoue, R., Miyashita, D., Li, J., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217815 · Cited by 14
Metadata
- Authors
- Titchenell, P. M., Chu, Q., Monks, B. R., & Birnbaum, M. J.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Birnbaum, Morris J.
- Venue
- Nature Communications
- Published
- 2015-05-12
- Volume
- 6
- Issue
- 1
- Pages
- 7078-7078
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC4429930
- OpenAlex
- W240175869
- Cited by
- 169
- References
- 43
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 11 · 2023: 14 · 2022: 18 · 2021: 15 · 2020: 15 · 2019: 11 · 2018: 19 · 2017: 24 · 2016: 14 · 2015: 8
- FWCI
- 9.41
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Nature Communications (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK056886, F32DK101175)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › FOXO transcription factor regulation
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Keywords
- hepatic glucose production, FOXO1, insulin receptor, Akt, gluconeogenesis, impaired glucose tolerance, insulin resistance, liver-specific knockout, postprandial glucose metabolism, hepatic glucose metabolism
- MeSH terms
- Forkhead Box Protein O1, Animals, Gene Expression Regulation, Gluconeogenesis, Glucose, Glucose Tolerance Test, Insulin Resistance, Liver, Male, Receptor, Insulin, RNA, Messenger, Signal Transduction, Mice, Knockout, Mice, Forkhead Transcription Factors
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