The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.
SIRT4 Has Tumor-Suppressive Activity and Regulates the Cellular Metabolic Response to DNA Damage by Inhibiting Mitochondrial Glutamine Metabolism
Open accessAbstract
DNA damage elicits a cellular signaling response that initiates cell cycle arrest and DNA repair. Here, we find that DNA damage triggers a critical block in glutamine metabolism, which is required for proper DNA damage responses. This block requires the mitochondrial SIRT4, which is induced by numerous genotoxic agents and represses the metabolism of glutamine into tricarboxylic acid cycle. SIRT4 loss leads to both increased glutamine-dependent proliferation and stress-induced genomic instability, resulting in tumorigenic phenotypes. Moreover, SIRT4 knockout mice spontaneously develop lung tumors. Our data uncover SIRT4 as an important component of the DNA damage response pathway that orchestrates a metabolic block in glutamine metabolism, cell cycle arrest, and tumor suppression.
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
“Moreover, evidence has shown that during the DNA damage response, normal cells show a decrease in glutaminolysis controlled by SIRT4 protein suppressing GLUD1. In the absence of SIRT4, a failure to undergo cell cycle arrest induced by DNA damage causes a delay in DNA repair and increased chromosomal instability, suggesting a tumor suppressor effect of SIRT4151.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [151]
In the citing paper
“Accordingly, loss of SIRT4 enhances glutamine-dependent proliferation and genomic instability, which simultaneously contribute to tumorigenesis151.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [151]
In the citing paper
“Similarly, SIRT4 is upregulated as part of the DNA damage response via ATF4 (Jeong et al. 2013).”
From The Mitochondrial Acylome Emerges: Proteomics, Regulation by Sirtuins, and Metabolic and Disease Implications (2018) · cites this paper as Jeong et al. 2013
In the citing paper
“SIRT4 likewise appears to control tumorigenesis ((Jeong et al. 2013), (Csibi et al. 2013)) by inhibiting the high rate of glutamine metabolism associated with cancer growth;”
From The Mitochondrial Acylome Emerges: Proteomics, Regulation by Sirtuins, and Metabolic and Disease Implications (2018) · cites this paper as Jeong et al. 2013
In the citing paper
“DHODH activity is also elevated in response to DNA damage and upon genotoxic chemotherapy treatment to increase nucleotide synthesis for DNA repair.76,77”
From The multifaceted contributions of mitochondria to cellular metabolism (2018) · cites this paper as [76]
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
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139
Rogakou, E. P., Pilch, D. R., Orr, A. H., Ivanova, V. S., & Bonner, W. M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.10.5858 · Cited by 5,438
The DNA Damage Response: Making It Safe to Play with Knives
Ciccia, A., & Elledge, S. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.019 · Cited by 4,368
Otto Warburg's contributions to current concepts of cancer metabolism
Koppenol, W. H., Bounds, P. L., & Dang, C. V. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3038 · Cited by 3,427
p21 in cancer: Intricate networks and multiple activities
Abbas, T., & Dutta, A. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2657 · Cited by 2,712
hSIR2SIRT1 Functions as an NAD-Dependent p53 Deacetylase
Vaziri, H., Dessain, S. K., Eaton, E. N., Imai, S., Frye, R. A., Pandita, T. K., Guarente, L., & Weinberg, R. A. (2001) · Cell · doi:10.1016/s0092-8674(01)00527-x · Cited by 2,690
DeBerardinis, R. J., Mancuso, A., Daikhin, E., Nissim, I., Yudkoff, M., Wehrli, S., & Thompson, C. B. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709747104 · Cited by 2,622
Genomic instability — an evolving hallmark of cancer
Negrini, S., Gorgoulis, V. G., & Halazonetis, T. D. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2858 · Cited by 2,397
Regulation of glutathione synthesis
Lu, S. C.-L. (2008) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2008.05.005 · Cited by 2,131
Sirtuins as regulators of metabolism and healthspan
Houtkooper, R. H., Pirinen, E., & Auwerx, J. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3293 · Cited by 2,008
Cell cycle checkpoint signaling through the ATM and ATR kinases
Abraham, R. T. (2001) · Genes & Development · doi:10.1101/gad.914401 · Cited by 1,966
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 446
Huang, R., Yu, Y., Zong, X., Li, X., Ma, L., & Zheng, Q. (2017) · Cancer Letters · doi:10.1016/j.canlet.2016.12.038 · Cited by 37
Tong, Y., Kai, J., Wang, S., Yu, Y., Xie, S., Zheng, H., Wang, Y., Liu, Y., Zhu, K., Guan, X., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03901-7 · Cited by 37
Xing, J., Li, J., Fu, L., Gai, J., Guan, J., & Li, Q. (2019) · Cancer Medicine · doi:10.1002/cam4.2557 · Cited by 36
Lovy, A., Ahumada-Castro, U., Bustos, G., Farías, P., González-Billault, C. E., Molgó, J., & Cárdenas, C. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00378 · Cited by 37
Sirtuins, aging, and cardiovascular risks
Favero, G., Franceschetti, L., Rodella, L. F., & Rezzani, R. (2015) · AGE · doi:10.1007/s11357-015-9804-y · Cited by 36
Rytelewski, M., Tong, J., Buensuceso, A. V., Leong, H. S., Vareki, S. M., Figueredo, R., Cresce, C. D., Wu, S. Y., Herbrich, S. M., Baggerly, K., et al. (2014) · Molecular Oncology · doi:10.1016/j.molonc.2014.05.017 · Cited by 36
SIRT4 Is a Regulator of Insulin Secretion
Zaganjor, E., Vyas, S., & Haigis, M. C. (2017) · Cell chemical biology · doi:10.1016/j.chembiol.2017.06.002 · Cited by 35
Self-citationAmino acids downregulate SIRT4 to detoxify ammonia through the urea cycle
Hu, S.-H., Feng, Y.-Y., Yang, Y.-X., Ma, H., Zhou, S.-X., Qiao, Y.-N., Zhang, K.-H., Zhang, L., Huang, L., Yuan, Y., et al. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00784-0 · Cited by 40
Self-citationFan, H., Xu, Z., Yao, K., Zheng, B., Zhang, Y., Wang, X., Zhang, T., Li, X., Hu, H., Yue, B., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-23-1443 · Cited by 36
Self-citationMolecular Sentinels: Unveiling the Role of Sirtuins in Prostate Cancer Progression
Chouhan, S., Muhammad, N., Usmani, D., Khan, T. H., & Kumar, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms26010183 · Cited by 34
Sirt1 protects from K‐Ras‐driven lung carcinogenesis
Costa‐Machado, L. F., Martín‐Hernández, R., Sánchez‐Luengo, M. Á., Hess, K., Vales‐Villamarín, C., Barradas, M., Lynch, C. J., de la Nava, D., Díaz‐Ruiz, A., de Cabo, R., et al. (2018) · EMBO Reports · doi:10.15252/embr.201643879 · Cited by 34
Jiang, W., Ouyang, X., Ji, Z., Shi, W., Wu, Y., Yao, Q., Wang, Y., Yang, W., Xiang, L., & Yang, H. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216064 · Cited by 34
Mito-Nuclear Communication in Hepatocellular Carcinoma Metabolic Rewiring
Mello, T., Simeone, I., & Galli, A. (2019) · Cells · doi:10.3390/cells8050417 · Cited by 34
Role of Sirtuins in Maintenance of Genomic Stability: Relevance to Cancer and Healthy Aging
Wu, X., Neng, C., Fenech, M. F., & Wang, X. (2016) · DNA and Cell Biology · doi:10.1089/dna.2016.3280 · Cited by 33
Self-citationOverexpression of SIRT4 inhibits the proliferation of gastric cancer cells through cell cycle arrest
Hu, Y., Lin, J., Lin, Y., Chen, X., Zhu, G., & Huang, G. (2018) · Oncology Letters · doi:10.3892/ol.2018.9877 · Cited by 32
Sirtuin Deacetylases as Therapeutic Targets in the Nervous System
Langley, B. C., & Sauve, A. A. (2013) · Neurotherapeutics · doi:10.1007/s13311-013-0214-5 · Cited by 33
Targeting Pulmonary Fibrosis by SLC1A5-Dependent Glutamine Transport Blockade
Choudhury, M., Schaefbauer, K. J., Kottom, T. J., Yi, E. S., Tschumperlin, D. J., & LIMPER, A. H. (2023) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2022-0339oc · Cited by 33
A Rice Glutamyl-tRNA Synthetase Modulates Early Anther Cell Division and Patterning
Yang, X., Li, G., Tian, Y., Song, Y., Liang, W., & Zhang, D. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.00110 · Cited by 32
Mechri, S., Sellem, I., Bouacem, K., Jabeur, F., Laribi-Habchi, H., Mellouli, L., Hacène, H., Bouanane‐Darenfed, A., & Jaouadi, B. (2020) · Environmental Science and Pollution Research · doi:10.1007/s11356-020-08076-w · Cited by 32
Bergmann, L., Lang, A., Bross, C., Altinoluk-Hambüchen, S., Fey, I., Overbeck, N., Stefanski, A., Wiek, C., Kefalas, A., Verhülsdonk, P., et al. (2020) · Cells · doi:10.3390/cells9091950 · Cited by 32
SZC-6, a small-molecule activator of SIRT3, attenuates cardiac hypertrophy in mice
Li, Z., Lu, G., Lü, J., Wang, P., Zhang, X., Zou, Y., & Liu, P. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-00966-8 · Cited by 32
Sirtuins in macrophage immune metabolism: A novel target for cardiovascular disorders
Xu, C.-Q., Li, J., Liang, Z., Zhong, Y.-L., Zhang, Z., Hu, X., Cao, Y., & Chen, J. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.128270 · Cited by 32
Serine hydroxymethyltransferase 2: a novel target for human cancer therapy
Xie, M., & Pei, D. (2021) · Investigational New Drugs · doi:10.1007/s10637-021-01144-z · Cited by 30
Avilkina, V., Chauveau, C., & Mhenni, O. G. (2021) · Bone · doi:10.1016/j.bone.2021.116232 · Cited by 33
The Mechanistic Roles of Sirtuins in Breast and Prostate Cancer
Onyiba, C. I., Scarlett, C. J., & Weidenhofer, J. (2022) · Cancers · doi:10.3390/cancers14205118 · Cited by 31
Sirtuins in Hematological Aging and Malignancy
Roth, M., Wang, Z., & Chen, W. (2013) · Critical Reviews™ in Oncogenesis · doi:10.1615/critrevoncog.2013010187 · Cited by 31
Tsusaka, T., Guo, T., Yagura, T., Inoue, T., Yokode, M., Inagaki, N., & Kondoh, H. (2014) · Genes to Cells · doi:10.1111/gtc.12176 · Cited by 31
Sirtuin 3 in renal diseases and aging: From mechanisms to potential therapies
Xuan, P., Ni, H., Kuang, B., Wang, Z., Hou, S., Gu, S., & Gong, N. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107261 · Cited by 33
Amino acid metabolism in breast cancer: pathogenic drivers and therapeutic opportunities
Liu, Y., Zong, X., Altea‐Manzano, P., & Fu, J. (2025) · Protein & Cell · doi:10.1093/procel/pwaf011 · Cited by 32
Mitochondrial sirtuins, key regulators of aging
Ji, Z., Liu, G., & Qu, J. T. (2025) · Life Medicine · doi:10.1093/lifemedi/lnaf019 · Cited by 32
Ramadani‐Muja, J., Gottschalk, B., Pfeil, K., Burgstaller, S., Rauter, T., Bischof, H., Waldeck‐Weiermair, M., Bugger, H., Graier, W. F., & Malli, R. (2019) · Cells · doi:10.3390/cells8121583 · Cited by 32
Monteiro‐Reis, S., Lameirinhas, A., Miranda‐Gonçalves, V., Felizardo, D., Dias, P. C., Oliveira, J., Graça, I. C. R., Gonçalves, C. S., Costa, B. M., Henrique, R., et al. (2020) · Cancers · doi:10.3390/cancers12051066 · Cited by 31
Implications of NAD + boosters in translational medicine
Kang, B. E., Choi, J., Stein, S., & Ryu, D. (2020) · European Journal of Clinical Investigation · doi:10.1111/eci.13334 · Cited by 32
Mitochondrial sirtuins in stem cells and cancer
Jaiswal, A., Xudong, Z., Ju, Z., & Saretzki, G. C. (2021) · FEBS Journal · doi:10.1111/febs.15879 · Cited by 29
Chen, L., Cui, H., Fang, J., Deng, H., Kuang, P., Guo, H., Wang, X., & Zhao, L. (2016) · Oncotarget · doi:10.18632/oncotarget.10579 · Cited by 30
Self-citationFatty acid oxidation facilitates DNA double-strand break repair by promoting PARP1 acetylation
Yang, S., Hwang, S., Kim, B.-J., Shin, S., Kim, M., & Jeong, S. M. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05968-w · Cited by 34
Self-citationLi, B., Chen, Q., Feng, Y., Wei, T., Zhang, Y., Zhang, Y., & Feng, Q. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216424 · Cited by 31
SIRT4 prevents excitotoxicity via modulating glutamate metabolism in glioma cells
Dönmez, G., & Colak, M. (2020) · Human & Experimental Toxicology · doi:10.1177/0960327120907142 · Cited by 29
Emerging strategies to target cancer metabolism and improve radiation therapy outcomes
Kery, M., & Papandreou, I. (2020) · British Journal of Radiology · doi:10.1259/bjr.20200067 · Cited by 33
Targeting respiratory complex I to prevent the Warburg effect
Vatrinet, R., Iommarini, L., Kurelac, I., Luise, M. D., Gasparre, G., & Porcelli, A. M. (2015) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2015.01.017 · Cited by 31
Endothelial dysfunction in the aging kidney
Borri, M., Jacobs, M. E., Carmeliet, P., Rabelink, T. J., & Dumas, S. J. (2025) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00287.2024 · Cited by 31
Regulation of Adaptive Immune Cells by Sirtuins
Warren, J. L., & MacIver, N. J. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00466 · Cited by 30
NAD metabolism in aging and cancer
Kincaid, J. W. R., & Berger, N. A. (2020) · Experimental Biology and Medicine · doi:10.1177/1535370220929287 · Cited by 29
The research progress on radiation resistance of cervical cancer
Liang, M., Sheng, L., Ke, Y., & Wu, Z. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1380448 · Cited by 28
Zhang, L., Yang, Y., Li, Y., Wang, C., Bian, C., Wang, H., & Wang, F. (2025) · Biomarker Research · doi:10.1186/s40364-025-00788-w · Cited by 28
Self-citationTargeting Mitochondrial Sirtuins in Age-Related Neurodegenerative Diseases and Fibrosis
Xiao, H., Xie, Y., Xi, K., Xie, J., Liu, M., Zhang, Y., Cheng, Z., Wang, W., Guo, B., & Wu, S. (2023) · Aging and Disease · doi:10.14336/ad.2023.0203 · Cited by 29
TRIM2 regulates the development and metastasis of tumorous cells of osteosarcoma
Qin, Y., Ye, J., Zhao, F., Hu, S., & Wang, S. (2018) · International Journal of Oncology · doi:10.3892/ijo.2018.4494 · Cited by 27
Zhang, Q., Qin, Y., Sun, X., Bian, Z., Liu, H., Liu, H., Mao, L., & Sun, S. (2024) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2024.111227 · Cited by 33
Sirtuins, a key regulator of ageing and age-related neurodegenerative diseases
Bhatt, V., & Tiwari, A. K. (2023) · International Journal of Neuroscience · doi:10.1080/00207454.2022.2057849 · Cited by 28
Sirtuins: Promising Therapeutic Targets to Treat Ischemic Stroke
Liu, Y., Wang, L., Yang, G., Chi, X., Liang, X., & Zhang, Y. (2023) · Biomolecules · doi:10.3390/biom13081210 · Cited by 26
Exploiting aneuploidy-imposed stresses and coping mechanisms to battle cancer
Zhou, L., Jilderda, L. J., & Foijer, F. (2020) · Open Biology · doi:10.1098/rsob.200148 · Cited by 30
m6A/IGF2BP3-driven serine biosynthesis fuels AML stemness and metabolic vulnerability
Huang, F., Wang, Y., Zhang, X., Gao, W., Li, J., Yang, Y., Mo, H., Prince, E. A., Long, Y., Hu, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58966-1 · Cited by 26
Regulation of Cancer and Cancer-Related Genes via NAD +
Sharif, T., Martell, E., Dai, C., Ghassemi-Rad, M. S., Kennedy, B. E., Lee, P. W. K., & Gujar, S. A. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7478 · Cited by 25
Addabbo, F., Chen, Q., Patel, D., Rabadi, M. M., Ratliff, B. B., Zhang, F., Jasmin, J.-F., Wolin, M. S., Lisanti, M. P., Gross, S. S., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065458 · Cited by 26
Effect of Resveratrol on Sirtuins, OPA1, and Fis1 Expression in Adult Zebrafish Retina
Sheng, W., Lu, Y., Feng, M., Wang, N., Liu, Z.-Z., Han, Y., Wang, H.-T., Zou, S., Xu, H. A., & Zhang, X. (2018) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.18-24539 · Cited by 25
Interplay Between the Circadian Clock and Sirtuins
Zhuang, Y., Zhang, Y., Liu, C., & Zhong, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111469 · Cited by 25
Coenzyme Q10 Supplement Rescues Postovulatory Oocyte Aging by Regulating SIRT4 Expression
Su, J., Xing, X., Zhang, J., Zhang, J., Wang, Y., Wang, J., Kang, J., Quan, F., & Zhang, Y. (2021) · Current Molecular Pharmacology · doi:10.2174/1874467214666210420112819 · Cited by 24
Zhang, F., Wang, D., Li, J., Su, Y., Liu, S., Lei, Q., & Yin, M. (2022) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjac020 · Cited by 26
Eldridge, M. J. G., & Hamon, M. A. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1010173 · Cited by 25
Intersections between mitochondrial sirtuin signaling and tumor cell metabolism
Herrera, K. N. G., Lee, J. J., & Haigis, M. C. (2015) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2015.1031879 · Cited by 25
Self-citationMammalian Sirtuins SIRT4 and SIRT7
Li, S., & Zheng, W. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.11.001 · Cited by 24
Knockout of SIRT4 decreases chemosensitivity to 5‑FU in colorectal cancer cells
Zhu, Y., Wang, G., Li, X., Wang, T., Weng, M., & Zhang, Y. (2018) · Oncology Letters · doi:10.3892/ol.2018.8850 · Cited by 24
Lv, M., Yang, X., Xu, C., Song, Q., Zhao, H., Sun, T., Liu, J., Zhang, Y., Sun, G., Xue, Y., et al. (2025) · Advanced Science · doi:10.1002/advs.202412553 · Cited by 29
Flavonoids as Sirtuin Modulators
Şenol, F. S., Eren, G., & Orhan, İ. E. (2022) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026622666220422094744 · Cited by 24
Exploring the Multi-Faceted Role of Sirtuins in Glioblastoma Pathogenesis and Targeting Options
Kunadis, E., & Piperi, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232112889 · Cited by 23
Sirtuin 4 Regulates Lipopolysaccharide Mediated Leydig Cell Dysfunction
Ramatchandirin, B., Sadasivam, M., Kannan, A., & Prahalathan, C. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25374 · Cited by 23
Biology, Chemistry, and Pharmacology of Sirtuins
Bedalov, A., Chowdhury, S., & Simon, J. A. (2016) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2016.03.011 · Cited by 23
Co-Operation between Aneuploidy and Metabolic Changes in Driving Tumorigenesis
Newman, D. L., & Gregory, S. L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184611 · Cited by 24
Cui, Y., Bai, Y., Yang, J., Yao, Y., Zhang, C., Liu, C., Shi, J., Li, Q., Zhang, J., Lü, X., et al. (2020) · Carcinogenesis · doi:10.1093/carcin/bgaa134 · Cited by 22
Alterations of sirtuins in mitochondrial cytochrome c-oxidase deficiency
Potthast, A. B., Heuer, T., Warneke, S. J., & Das, A. M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186517 · Cited by 22
The signaling pathways that mediate the anti-cancer effects of caloric restriction
Lu, Y., Tao, F., Zhou, M., & Tang, K. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.01.021 · Cited by 24
Functions of mammalian SIRT4 in cellular metabolism and research progress in human cancer (Review)
Wang, C., Liu, Y., Zhu, Y., & Kong, C. (2020) · Oncology Letters · doi:10.3892/ol.2020.11872 · Cited by 24
Xu, M., Hou, Y., Li, N., Yu, W., & Chen, L. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05169-9 · Cited by 22
Epigenomic and Metabolomic Integration Reveals Dynamic Metabolic Regulation in Bladder Cancer
Loras, A., Segovia, C., & Ruiz-Cerdá, J. L. (2021) · Cancers · doi:10.3390/cancers13112719 · Cited by 23
Schistosome Sirtuins as Drug Targets
Lancelot, J., Cabezas‐Cruz, A., Caby, S., Marek, M., Schultz, J., Romier, C., Sippl, W., Jung, M., & Pierce, R. J. (2015) · Future Medicinal Chemistry · doi:10.4155/fmc.15.24 · Cited by 22
Qin, X., Tatsukawa, H., Hitomi, K., Shirakami, Y., Ishibashi, N., Shimizu, M., Moriwaki, H., & Kojima, S. (2016) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-15-0326 · Cited by 20
Multifaced role of protein deacetylase sirtuins in neurodegenerative disease
Gupta, R. V., Ambasta, R. K., & Kumar, P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.047 · Cited by 20
Mitochondrial Alterations in Prostate Cancer: Roles in Pathobiology and Racial Disparities
Vikramdeo, K. S., Sharma, A., Anand, S., Sudan, S. K., Singh, S., Singh, A. P., & Dasgupta, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054482 · Cited by 20
Tumor-suppressive function of SIRT4 in neuroblastoma through mitochondrial damage
Wang, Y., Guo, Y., Gao, J., & Yuan, X. (2018) · Cancer Management and Research · doi:10.2147/cmar.s172509 · Cited by 20
Research Progress of Sirtuin4 in Cancer
Bai, Y., Yang, J., Cui, Y., Yao, Y., Wu, F., Liu, C., Fan, X., & Zhang, Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.562950 · Cited by 20
Bang, S., Choi, S.-H., & Jeong, S. M. (2025) · Cells · doi:10.3390/cells14241956 · Cited by 22
Self-citationLee, S. M., Lee, G., & Kim, H. U. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.06.027 · Cited by 18
He, L., Liu, Q., Cheng, J., Cao, M., Zhang, S., Wan, X., Li, J., & Tu, H. (2023) · Biogerontology · doi:10.1007/s10522-023-10022-5 · Cited by 18
Metabolic Alterations at the Crossroad of Aging and Oncogenesis
Raffaghello, L., & Longo, V. D. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.01.003 · Cited by 19
Mechri, S., Sellem, I., Bouacem, K., Jabeur, F., Chamkha, M., Hacène, H., Bouanane‐Darenfed, A., & Jaouadi, B. (2020) · Waste and Biomass Valorization · doi:10.1007/s12649-020-00942-5 · Cited by 18
Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
He, Q., Chen, K., Ye, R., Dai, N., Guo, P., & Wang, L. (2020) · Oncology Letters · doi:10.3892/ol.2020.11432 · Cited by 18
Bhalla, K., Jaber, S. M., Reagan, K., Hamburg, A., Underwood, K. F., Jhajharia, A., Singh, M., Bhandary, B., Bhat, S., Nanaji, N. M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-78193-6 · Cited by 17
Chen, X., Lai, X., Wu, C., Tian, Q., Lei, T., Pan, J., & Huang, G. (2017) · Cancer Biomarkers · doi:10.3233/cbm-160419 · Cited by 18
Lin, R., Zhu, Y., Liu, Y.-J., Guo, Z., Wei, J., Li, Y., & Yu, Y. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107936 · Cited by 18
Self-citationZhao, X., Shao, Z., Zhou, X., Lin, Y., Guo, J., Guo, J., Zhang, Y., & Wang, S. (2021) · Food and Chemical Toxicology · doi:10.1016/j.fct.2021.112249 · Cited by 17
STAT3 Signaling Axis and Tamoxifen in Breast Cancer: A Promising Target for Treatment Resistance
Zamanian, M. Y., Golmohammadi, M., Al‐Alak, A., Kamiab, Z., Obaid, R. F., Ramírez‐Coronel, A. A., Hjazi, A. M., Abosaooda, M., Mustafa, Y. F., Heidari, M., et al. (2023) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520623666230713101119 · Cited by 17
Tucker, S. A., Hu, S.-H., Vyas, S., Park, A., Joshi, S., Inal, A., Lam, T., Tan, E., Haigis, K. M., & Haigis, M. C. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113975 · Cited by 18
Self-citationCai, G., Ge, Z., Xu, Y., Cai, L., Sun, P., & Huang, G. (2022) · Scientific Reports · doi:10.1038/s41598-022-16610-8 · Cited by 17
Huang, G., Lin, Y., & Zhu, G. (2017) · PubMed Central · Cited by 16
Regulation of metabolic reprogramming by tumor suppressor genes in pancreatic cancer
Liu, M., Liu, W., Qin, Y., Xu, X., Yu, X., Zhuo, Q., & Ji, S. (2020) · Experimental Hematology and Oncology · doi:10.1186/s40164-020-00179-x · Cited by 17
Self-citationKim, B.-J., Gwak, J., Kim, M., Yang, S., Hwang, S., Shin, S., Kim, J. H., Son, J., & Jeong, S. M. (2023) · Cancer Gene Therapy · doi:10.1038/s41417-023-00598-y · Cited by 16
Self-citationMetabolic regulation of endothelial senescence
Le, N.-T. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1232681 · Cited by 15
Right on TARGET: glutamine metabolism in cancer
Ratnikov, B. I., Jeon, Y. J., Smith, J. W., & Ronai, Z. A. (2015) · Oncoscience · doi:10.18632/oncoscience.205 · Cited by 15
Yokoyama, N. N., Denmon, A. P., Uchio, E., Jordan, M. L., Mercola, D., & Zi, X. (2015) · Current Pharmacology Reports · doi:10.1007/s40495-015-0039-5 · Cited by 15
The possible role of sirtuins in male reproduction
Loganathan, C., Kannan, A., Panneerselvam, A., Mariajoseph-Antony, L. F., Kumar, S. A., Kumarasamy, A., & Prahalathan, C. (2021) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-021-04116-2 · Cited by 14
Metadata
- Authors
- Jeong, S. M., Xiao, C., Finley, L. W. S., Lahusen, T., Souza, A. L., Pierce, K., Li, Y.-H., Wang, X., Laurent, G., German, N. J., Xu, X., Li, C., Wang, R.-H., Lee, J., Csibi, A., Cerione, R., Blenis, J., Clish, C. B., Kimmelman, A., Deng, C.-X., & Haigis, M. C.
- Affiliations
- Harvard University (US)
- National Institutes of Health (US)
- Broad Institute (US)
- Cornell University (US)
- Corresponding author
- Deng, Chu-Xia
- Haigis, Marcia C.
- ORCID
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2013-04
- Volume
- 23
- Issue
- 4
- Pages
- 450-463
- ISSN
- 1535-6108 (ISSN-L)
- PMC
- PMC3650305
- OpenAlex
- W2046120998
- Cited by
- 445
- References
- 56
- Citations by year
- 2026: 9 · 2025: 31 · 2024: 27 · 2023: 28 · 2022: 33 · 2021: 43 · 2020: 42 · 2019: 31 · 2018: 41 · 2017: 32 · 2016: 41 · 2015: 38 · 2014: 24 · 2013: 23
- FWCI
- 19.64
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cancer Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (R01AG032375, AG032375)
- National Cancer Institute (R01CA157490)
- Topics
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- SIRT4, DNA damage response, glutamine metabolism, mitochondrial metabolism, TCA cycle, tumor suppression, genomic instability, cell cycle arrest, lung cancer, genotoxic stress, tumor suppressor
- MeSH terms
- Animals, DNA Damage, DNA Repair, Female, Glutamine, Humans, Male, Mitochondria, Neoplasms, Experimental, Signal Transduction, Mice, Knockout, Mitochondrial Proteins, Tumor Suppressor Proteins, Sirtuins, Cell Line, Tumor, Cell Growth Processes, Mice, Hep G2 Cells, HEK293 Cells
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