The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Telomerase directly regulates NF-κB-dependent transcription
Abstract
Although elongation of telomeres is thought to be the prime function of reactivated telomerase in cancers, this activity alone does not account for all of the properties that telomerase reactivation attributes to human cancer cells. Here, we uncover a link between telomerase and NF-κB, a master regulator of inflammation. We observe that while blocking NF-κB signalling can inhibit effects of telomerase overexpression on processes relevant to transformation, increasing NF-κB activity can functionally substitute for reduced telomerase activity. Telomerase directly regulates NF-κB-dependent gene expression by binding to the NF-κB p65 subunit and recruitment to a subset of NF-κB promoters such as those of IL-6 and TNF-α, cytokines that are critical for inflammation and cancer progression. As NF-κB can transcriptionally upregulate telomerase levels, our findings suggest that a feed-forward regulation between them could be the key mechanistic basis for the coexistence of chronic inflammation and sustained telomerase activity in human cancers.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“It has to be noted though that apart from initiating replicative immortality, telomerase seems to play a crucial role in almost all the hallmarks of cancer, ranging from cell growth and proliferation through to the activation of EGFR signaling [182], resistance to apoptosis through activation of NF-kB [183], and the promotion of invasion and metastasis through induction of the epithelial–mesenchym”
From Current and Future Trends of Colorectal Cancer Treatment: Exploring Advances in Immunotherapy (2024) · cites this paper as [183]
Citations
Cites
Hallmarks of Cancer: The Next Generation
Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590
Mantovani, A., Allavena, P., Sica, A., & Balkwill, F. (2008) · Nature · doi:10.1038/nature07205 · Cited by 11,399
The Human Genome Browser at UCSC
Kent, W. J., Sugnet, C. W., Furey, T. S., Roskin, K. M., Pringle, T. H., Zahler, A. M., & Haussler, A. D. (2002) · Genome Research · doi:10.1101/gr.229102 · Cited by 10,400
The limited in vitro lifetime of human diploid cell strains
Hayflick, L. (1965) · Experimental Cell Research · doi:10.1016/0014-4827(65)90211-9 · Cited by 5,876
Shared Principles in NF-κB Signaling
Hayden, M. S., & Ghosh, S. (2008) · Cell · doi:10.1016/j.cell.2008.01.020 · Cited by 4,954
GREAT improves functional interpretation of cis-regulatory regions
McLean, C. Y., Bristor, D., Hiller, M., Clarke, S. L., Schaar, B. T., Lowe, C. B., Wenger, A. M., & Bejerano, G. (2010) · Nature Biotechnology · doi:10.1038/nbt.1630 · Cited by 4,502
Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1
Barbie, D. A., Tamayo, P., Boehm, J. S., Kim, S. Y., Moody, S. E., Dunn, I. F., Schinzel, A. C., Sandy, P., Meylan, E., Scholl, C., et al. (2009) · Nature · doi:10.1038/nature08460 · Cited by 3,922
Suppression of TNF-α-Induced Apoptosis by NF-κB
Antwerp, D. J. V., Martin, S. J., Kafri, T., Green, D. R., & Verma, I. M. (1996) · Science · doi:10.1126/science.274.5288.787 · Cited by 2,581
NF-κB functions as a tumour promoter in inflammation-associated cancer
Pikarsky, E., Porat, R. M., Stein, I., Abramovitch, R., Amit, S., Kasem, S., Gutkovich-Pyest, E., Urieli-Shoval, S., Galun, E., & Ben‐Neriah, Y. (2004) · Nature · doi:10.1038/nature02924 · Cited by 2,423
Integrating cell-signalling pathways with NF-κB and IKK function
Perkins, N. D. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2083 · Cited by 2,350
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 378
Telomeres in neurological disorders
Anitha, A., Thanseem, I., Vasu, M. M., Viswambharan, V., & Poovathinal, S. A. (2019) · Advances in clinical chemistry · doi:10.1016/bs.acc.2019.01.003 · Cited by 49
Emerging mechanisms of telomerase reactivation in cancer
Sharma, S., & Chowdhury, S. (2022) · Trends in cancer · doi:10.1016/j.trecan.2022.03.005 · Cited by 48
Efficient DNA binding of NF-κB requires the chaperone-like function of NPM1
Lin, J., Kato, M., Nagata, K., & Okuwaki, M. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1285 · Cited by 47
Telomerase stimulates ribosomal DNA transcription under hyperproliferative conditions
Gonzalez, O. G., Assfalg, R., Koch, S., Schelling, A., Meena, J. K., Kraus, J. M., Lechel, A., Katz, S., Beneš, V., Scharffetter‐Kochanek, K., et al. (2014) · Nature Communications · doi:10.1038/ncomms5599 · Cited by 46
PES1 is a critical component of telomerase assembly and regulates cellular senescence
Cheng, L., Yuan, B., Ying, S., Niu, C., Mai, H.-X., Guan, X., Yang, X., Teng, Y., Lin, J., Huang, J., et al. (2019) · Science Advances · doi:10.1126/sciadv.aav1090 · Cited by 47
The Maintenance of Telomere Length in CD28+ T Cells During T Lymphocyte Stimulation
Huang, E. E., Tedone, E., O’Hara, R. A., Cornelius, C., Lai, T., Ludlow, A. T., Wright, W. E., & Shay, J. W. (2017) · Scientific Reports · doi:10.1038/s41598-017-05174-7 · Cited by 46
Cai, Y., Kandula, V., Kosuru, R., Ye, X., Irwin, M. G., & Xia, Z. (2017) · Cell Cycle · doi:10.1080/15384101.2017.1371886 · Cited by 46
El-Badawy, A., Ghoneim, N. I., Nasr, M. A., Elkhenany, H. A., Ahmed, T. A., Ahmed, S. M., & El‐Badri, N. (2018) · Biology Open · doi:10.1242/bio.034181 · Cited by 44
Telomere Length: A Cardiovascular Biomarker and a Novel Therapeutic Target
Sagris, Μ., Theofilis, P., Antonopoulos, A. S., Tsioufis, K. P., & Tousoulis, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232416010 · Cited by 44
Liu, S., Nong, W., Ji, L., Zhuge, X., Wei, H., Luo, M., Zhou, L., Chen, S., Zhang, S., Lei, X., et al. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112132 · Cited by 47
Teichroeb, J. H., Kim, J., & Betts, D. H. (2016) · RNA Biology · doi:10.1080/15476286.2015.1134413 · Cited by 46
Non-canonical roles of canonical telomere binding proteins in cancers
Akıncılar, S. C., Chan, C. H. T., Ng, Q. F., Fidan, K., & Tergaonkar, V. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03783-0 · Cited by 45
Self-citationSerrated colorectal cancer: preclinical models and molecular pathways
Aiderus, A., Barker, N., & Tergaonkar, V. (2023) · Trends in cancer · doi:10.1016/j.trecan.2023.09.011 · Cited by 42
Self-citationInhibition of RAP1 Enhances Corneal Recovery Following Alkali Injury
Poon, M.-W., Yan, L., Jiang, D., Qin, P., Tse, H., Wong, I. Y., Wong, D., Tergaonkar, V., & Lian, Q. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-15268 · Cited by 42
Self-citationMiller, J., Dakic, A., Chen, R., Palechor-Ceron, N., Dai, Y., Kallakury, B., Schlegel, R., & Liu, X. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003284 · Cited by 42
Song, H.-J., Chen, X., Jiao, Q., Qiu, Z., Shen, C., Zhang, G., Sun, Z., Zhang, H., & Luo, Q. (2020) · Thyroid · doi:10.1089/thy.2020.0023 · Cited by 42
The Role of Telomerase in Breast Cancer’s Response to Therapy
Judasz, E., Lisiak, N., Kopczyński, P., Taube, M., & Rubiś, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232112844 · Cited by 43
Significance of NF‐κB activation in immortalization of nasopharyngeal epithelial cells
Zhu, D. D., Zhang, J., Deng, W., Yip, Y. L., Lung, H. L., Tsang, C. M., Law, W. T., Yang, J., Lau, V. M. Y., Shuen, T. W. H., et al. (2015) · International Journal of Cancer · doi:10.1002/ijc.29850 · Cited by 43
A cascade amplification approach for visualization of telomerase activity in living cells
Yan, L., Hui, J., Liu, Y., Guo, Y., Liu, L., Ding, L., & Ju, H. (2016) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2016.07.102 · Cited by 41
Hexokinase 2 is a molecular bridge linking telomerase and autophagy
Roh, J.-I., Kim, Y.-J., Oh, J., Kim, Y., Lee, J., Lee, J., Chun, K., & Lee, H. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193182 · Cited by 41
Jacczak, B., Rubiś, B., & Totoń, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126381 · Cited by 43
Soutto, M., Chen, Z., Katsha, A. M., Romero–Gallo, J., Krishna, U. S., Piazuelo, M. B., Washington, M. K., Peek, R. M., Belkhiri, A., & El-Rifai, W. M. (2015) · Cancer · doi:10.1002/cncr.29644 · Cited by 40
Pan, Y., Meng, M., Zheng, N., Cao, Z., Yang, P., Xi, X., & Zhou, Q. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.11.024 · Cited by 41
González‐Giraldo, Y., Forero, D. A., Echeverría, V., García‐Segura, L. M., & Barreto, G. E. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.02.017 · Cited by 40
Zhang, X., Li, B., de Jonge, N., Björkholm, M., & Xu, D. (2015) · Oncotarget · doi:10.18632/oncotarget.2917 · Cited by 38
TERT promoter mutations in thyroid cancer
Matsuse, M., & Mitsutake, N. (2023) · Endocrine Journal · doi:10.1507/endocrj.ej23-0136 · Cited by 40
Telomerase activates transcription of cyclin D1 gene through an interaction with NOL1
Hong, J., Lee, J. H., & Chung, I. K. (2016) · Journal of Cell Science · doi:10.1242/jcs.181040 · Cited by 38
Current and Future Trends of Colorectal Cancer Treatment: Exploring Advances in Immunotherapy
Nikolouzakis, T. K., Chrysos, E., Docea, A. O., Fragkiadaki, P., Souglakos, J., Tsiaoussis, J., & Tsatsakis, A. (2024) · Cancers · doi:10.3390/cancers16111995 · Cited by 37
Loss of Telomere Protection: Consequences and Opportunities
Jacobs, J. J. L. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00088 · Cited by 40
Mechanistic Insights of Thyroid Cancer Progression
Leandro-Garcia, L. J., & Landa, I. (2023) · Endocrinology · doi:10.1210/endocr/bqad118 · Cited by 37
Saraswati, A. P., Relitti, N., Brindisi, M., Gemma, S., Zisterer, D. M., Butini, S., & Campiani, G. (2019) · Drug Discovery Today · doi:10.1016/j.drudis.2019.05.015 · Cited by 37
Telomerase promotes formation of a telomere protective complex in cancer cells
Perera, O. N., Sobinoff, A. P., Teber, E., Harman, A., Maritz, M. F., Yang, S. F., Pickett, H. A., Cesare, A. J., Arthur, J. W., MacKenzie, K. L., et al. (2019) · Science Advances · doi:10.1126/sciadv.aav4409 · Cited by 36
Telomerase in Brain: The New Kid on the Block and Its Role in Neurodegenerative Diseases
Saretzki, G. C., & Wan, T. (2021) · Biomedicines · doi:10.3390/biomedicines9050490 · Cited by 38
Giunco, S., Celeghin, A., Gianesin, K., Dolcetti, R., Indraccolo, S., & Rossi, A. D. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.145 · Cited by 36
Telomerase and hallmarks of cancer: An intricate interplay governing cancer cell evolution
Kumar, N., & Sethi, G. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216459 · Cited by 35
Snail1 transcription factor controls telomere transcription and integrity
Mazzolini, R., Gonzàlez, N., García-Garijo, A., Millanes‐Romero, A., Peiró, S., Smith, S. H., de Herreros, A. G., & Canudas, S. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx958 · Cited by 37
Ovarian Telomerase and Female Fertility
Toupance, S., Fattet, A.-J., Thornton, S. N., Bénétos, A., Guéant, J., & Koscinski, I. (2021) · Biomedicines · doi:10.3390/biomedicines9070842 · Cited by 36
TERT Extra-Telomeric Roles: Antioxidant Activity and Mitochondrial Protection
Marinaccio, J., Micheli, E., Udroiu, I., Nottia, M. D., Carrozzo, R., Baranzini, N., Grimaldi, A., Leone, S., Moreno, S., Muzzi, M., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054450 · Cited by 35
Gao, Z., Bravo, R., Rupert, J. E., Drunen, R. V., Yu, Y., Eckel‐Mahan, K. L., & Kolonin, M. G. (2024) · Aging Cell · doi:10.1111/acel.14138 · Cited by 35
Nasrollahzadeh, A., Bashash, D., Kabuli, M., Zandi, Z., Kashani, B., Zaghal, A., Mousavi, S. A., & Ghaffari, S. H. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118060 · Cited by 34
Plyasova, A. A., & Zhdanov, D. D. (2021) · Biomedicines · doi:10.3390/biomedicines9050526 · Cited by 35
Nair‐Shalliker, V., Dhillon, V. S., Clements, M., Armstrong, B. K., & Fenech, M. F. (2014) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2014.04.001 · Cited by 35
Functional and mechanistic analysis of telomerase: An antitumor drug target
Chen, Y., & Zhang, Y. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.03.017 · Cited by 36
Consensus transcriptional regulatory networks of coronavirus-infected human cells
Ochsner, S. A., Pillich, R., & McKenna, N. J. (2020) · Scientific Data · doi:10.1038/s41597-020-00628-6 · Cited by 35
Akıncılar, S. C., Chua, J. Y. H., Ng, Q. F., Chan, C. H. T., Eslami‐S, Z., Chen, K., Low, J.-L., Arumugam, S., Aswad, L., Chua, C., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac479 · Cited by 33
Self-citationNUCKS: a potential biomarker in cancer and metabolic disease
Qiu, B., Han, W., & Tergaonkar, V. (2015) · Clinical Science · doi:10.1042/cs20140656 · Cited by 34
Self-citationReview: NF-kB activation in canine cancer
Schlein, L. J., & Thamm, D. H. (2022) · Veterinary Pathology · doi:10.1177/03009858221092017 · Cited by 32
Otsubo, T., Yamada, K., Hagiwara, T., Oshima, K., Iida, K., Nishikata, K., Toyoda, T., Igari, T., Nohara, K., Yamashita, S., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.21375 · Cited by 32
Fatemi, A., Safa, M., & Kazemi, A. (2015) · Tumor Biology · doi:10.1007/s13277-015-3575-z · Cited by 32
Su, X., Jiang, X., Wang, W., Wang, H., Xu, X., Lin, A., Teng, X., Wu, H., & Teng, L. (2016) · OncoTargets and Therapy · doi:10.2147/ott.s116594 · Cited by 32
Ameri, Z., Ghiasi, S., Farsinejad, A., Hassanshahi, G., Ehsan, M., & Fatemi, A. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.04.060 · Cited by 32
The mechanism of NF-κB-TERT feedback regulation of granulosa cell apoptosis in PCOS rats
Xue, H., Hu, Z., Liu, S., Zhang, S., Yang, W., Li, J., Yan, C., Zhang, J., Zhang, J., & Lei, X. (2024) · PLoS ONE · doi:10.1371/journal.pone.0312115 · Cited by 30
Shetty, R., Kumar, N. R., Khamar, P. M., Francis, M., Sethu, S., Randleman, J. B., Krueger, R. R., Roy, A. S., & Ghosh, A. (2019) · Journal of Refractive Surgery · doi:10.3928/1081597x-20181128-01 · Cited by 30
Self-citationRole of telomerase in the tumour microenvironment
Liu, N., Guo, X., Liu, J., & Cong, Y. (2019) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13223 · Cited by 30
Multiple Actions of Telomerase Reverse Transcriptase in Cell Death Regulation
Palamarchuk, A. I., Kovalenko, E. I., & Streltsova, M. A. (2023) · Biomedicines · doi:10.3390/biomedicines11041091 · Cited by 31
Li, Y., & Tergaonkar, V. (2016) · Transcription · doi:10.1080/21541264.2016.1160173 · Cited by 30
Self-citationTelomeres, telomerase, and cancer: mechanisms, biomarkers, and therapeutics
Shou, S., Maolan, A., Zhang, D., Jiang, X., Liu, F., Li, Y., Zhang, X., Geer, E., Pu, Z., Hua, B., et al. (2025) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00597-9 · Cited by 29
Protsenko, E., Rehkopf, D. H., Prather, A. A., Epel, E. S., & Lin, J. (2020) · PLoS ONE · doi:10.1371/journal.pone.0240185 · Cited by 29
Targeted Covalent Inhibition of Telomerase
Betori, R. C., Liu, Y., Wu, D., Mishra, R., Cohen, S., Kron, S. J., & Scheidt, K. A. (2020) · ACS Chemical Biology · doi:10.1021/acschembio.9b00945 · Cited by 29
Means to the ends: The role of telomeres and telomere processing machinery in metastasis
Robinson, N. J., & Schiemann, W. P. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.10.005 · Cited by 28
Ci, X., Li, B., Ma, X., Kong, F., Zheng, C., Björkholm, M., Jia, J., & Xu, D. (2015) · Oncotarget · doi:10.18632/oncotarget.5752 · Cited by 27
Kotla, S., Le, N., Vu, H. T., Ko, K. A., Gi, Y. J., Thomas, T. N., Giancursio, C. J., Lusis, A. J., Cooke, J. P., Fujiwara, K., et al. (2019) · Metabolism · doi:10.1016/j.metabol.2019.153962 · Cited by 27
Piñeiro‐Hermida, S., Bosso, G., Sánchez-Vazquez, R., Martínez, P., & Blasco, M. A. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01149-6 · Cited by 28
Telomerase-targeted therapies in myeloid malignancies
Waksal, J. A., Bruedigam, C., Komrokji, R. S., Jamieson, C. H. M., & Mascarenhas, J. O. (2023) · Blood Advances · doi:10.1182/bloodadvances.2023009903 · Cited by 27
Telomerase Reverse Transcriptase Regulates microRNAs
Lassmann, T., Maida, Y., Tomaru, Y., Yasukawa, M., Ando, Y., Kojima, M., Kasim, V., Simon, C., Daub, C. O., Carninci, P., et al. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16011192 · Cited by 27
Cellular lifespan and senescence: a complex balance between multiple cellular pathways
Dolivo, D., Hernandez, S. J., & Dominko, T. (2016) · BioEssays · doi:10.1002/bies.201670906 · Cited by 29
Kachuri, L., Latifovic, L., Liu, G., & Hung, R. J. (2016) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-16-0200 · Cited by 27
Long-term ozone exposure is positively associated with telomere length in critically ill patients
Wang, C., Wolters, P. J., Calfee, C. S., Liu, S., Balmes, J. R., Zhao, Z., Koyama, T., & Ware, L. B. (2020) · Environment International · doi:10.1016/j.envint.2020.105780 · Cited by 27
Teralı, K., & Yılmazer, A. (2015) · Biochimie · doi:10.1016/j.biochi.2015.12.001 · Cited by 28
Role of Telomeres Shortening in Atherogenesis: An Overview
Yegorov, Y. E., Poznyak, A. V., Nikiforov, N. G., Starodubova, A. V., & Orekhov, A. N. (2021) · Cells · doi:10.3390/cells10020395 · Cited by 26
Prabhavathy, D., Chandrasekaran, K. S., & Karunagaran, D. (2015) · Bioscience Reports · doi:10.1042/bsr20140160 · Cited by 26
Many Functions of Telomerase Components: Certainties, Doubts, and Inconsistencies
Udroiu, I., Marinaccio, J., & Sgura, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315189 · Cited by 25
Telomerase reverse transcriptase and neurodegenerative diseases
Yu, X., Liu, M., Zheng, C., Liu, Y., Wang, Z., & Wang, Z.-Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1165632 · Cited by 25
Wu, Y. L., Bian, C., Zhen, C., Liu, L., Lin, Z., Nisar, M. F., Wang, M., Bartsch, J. W., Huang, E., Ji, P., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.20888 · Cited by 25
Staffaroni, A. M., Tosun, D., Lin, J., Elahi, F. M., Casaletto, K. B., Wynn, M. J., Patel, N., Neuhaus, J. M., Walters, S. M., Epel, E. S., et al. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.04.021 · Cited by 28
Wysoczańska, B., Dratwa, M., Gębura, K., Mizgala, J., Mazur, G. J., Wróbel, T., & Bogunia‐Kubik, K. (2019) · OncoTargets and Therapy · doi:10.2147/ott.s198313 · Cited by 25
Jeda, A. S., Badrzadeh, F., Esghaei, M., & Abdoli, A. (2021) · Cancer Treatment and Research Communications · doi:10.1016/j.ctarc.2021.100323 · Cited by 24
Telomere Length, TERT, and miRNA Expression
Slattery, M. L., Herrick, J. S., Pellatt, A. J., Wolff, R. K., & Mullany, L. E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162077 · Cited by 25
Landa, I., Thornton, C. E. M., Xu, B., Haase, J., Krishnamoorthy, G. P., Hao, J., Knauf, J. A., Herbert, Z. T., Martínez, P., Blasco, M. A., et al. (2023) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-23-0144 · Cited by 23
Telomerase Biology Associations Offer Keys to Cancer and Aging Therapeutics
Smith‐Sonneborn, J. (2019) · Current Aging Science · doi:10.2174/1874609812666190620124324 · Cited by 24
Romaniuk-Drapała, A., Totoń, E., Konieczna, N., Machnik, M., Barczak, W., Kowal, D., Kopczyński, P., Kaczmarek, M., & Rubiś, B. (2021) · Cells · doi:10.3390/cells10040867 · Cited by 23
Implications of telomerase reverse transcriptase in tumor metastasis
Zou, Y., Cong, Y., & Zhou, J. (2020) · BMB Reports · doi:10.5483/bmbrep.2020.53.9.108 · Cited by 22
Self-citationOverexpression of cellular telomerase RNA enhances virus-induced cancer formation
Kheimar, A., Trimpert, J., Groenke, N., & Kaufer, B. B. (2018) · Oncogene · doi:10.1038/s41388-018-0544-1 · Cited by 22
Long-lived termite kings and queens activate telomerase in somatic organs
Koubová, J., Pangrácová, M., Jankásek, M., Lukšan, O., Jehlík, T., Brabcová, J., Jedlička, P., Křivánek, J., Frydrychová, R. Č., & Hanus, R. (2021) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2021.0511 · Cited by 22
Ask, T. F., Lugo, R. G., & Sütterlin, S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00726 · Cited by 23
He, L., Zhang, X., Zhang, S., Wang, Y., Hu, W., Li, J., Liu, Y., Liao, Y., Peng, X., Li, J., et al. (2024) · Advanced Science · doi:10.1002/advs.202401227 · Cited by 21
Vinayagamurthy, S., Bagri, S., Mergny, J., & Chowdhury, S. (2022) · Trends in Genetics · doi:10.1016/j.tig.2022.10.002 · Cited by 21
hTERT promotes gastric intestinal metaplasia by upregulating CDX2 via NF-κB signaling pathway
Chen, B.-J., Zeng, S., Xie, R., Hu, C.-J., Wang, S.-M., Wu, Y., Xiao, Y., & Yang, S. (2017) · Oncotarget · doi:10.18632/oncotarget.15926 · Cited by 21
Human telomerase reverse transcriptase is a novel target of Hippo‐YAP pathway
Zhang, Q., Liu, N., Bai, J., Zhou, Q., Mao, J., Xu, L., Liu, J., Wei, H., Ren, C., Wu, X., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201902147r · Cited by 21
Liao, Y., Gao, Y., Chang, A., Li, Z., Wang, H., Cao, J., Gu, W., & Tang, R. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15854 · Cited by 21
Robinson, N. J., Miyagi, M., Scarborough, J. A., Scott, J. G., Taylor, D. J., & Schiemann, W. P. (2021) · Science Signaling · doi:10.1126/scisignal.abe9613 · Cited by 21
Błasiak, J., Szczepańska, J., Fila, M., Pawłowska, E., & Kaarniranta, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137194 · Cited by 22
Iron-(Fe3+)-Dependent Reactivation of Telomerase Drives Colorectal Cancers
Shanmugam, R., Majee, P., Shi, W., Ozturk, M. B., Vaiyapuri, T. S., Idzham, K., Raju, A., Shin, S. H., Fidan, K., Low, J.-L., et al. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-1379 · Cited by 20
Self-citationLe, T. Y. L., Pickett, H. A., Yang, A., Ho, J. W. K., Thavapalachandran, S., Igoor, S., Yang, S. F., Farraha, M., Voges, H. K., Hudson, J. E., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-47022-w · Cited by 20
Telomerase in hematologic malignancies
Bruedigam, C., & Lane, S. (2016) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000252 · Cited by 20
Fang, L., & Cui, J. (2015) · Medical Oncology · doi:10.1007/s12032-015-0649-0 · Cited by 20
Clonal inactivation of TERT impairs stem cell competition
Hasegawa, K., Zhao, Y., Garbuzov, A., Corces, M. R., Neuhöfer, P., Gillespie, V. M., Cheung, P., Belk, J. A., Huang, Y., Wei, Y., et al. (2024) · Nature · doi:10.1038/s41586-024-07700-w · Cited by 20
Mechanisms of TERT Reactivation and Its Interaction with BRAFV600E
Song, Y. S., & Park, Y. J. (2020) · Endocrinology and Metabolism · doi:10.3803/enm.2020.304 · Cited by 19
Robinson, N. J., Taylor, D. J., & Schiemann, W. P. (2019) · Journal of Cancer Metastasis and Treatment · doi:10.20517/2394-4722.2019.15 · Cited by 18
The Pivotal Role of NF-κB in Glioblastoma: Mechanisms of Activation and Therapeutic Implications
Ramar, V., Guo, S., Wang, G., & Liu, M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26167883 · Cited by 18
Metadata
- Authors
- Ghosh, A., Saginc, G., Leow, S. C., Khattar, E., Shin, E. M., Yan, T. D., Wong, M., Zhang, Z., Li, G., Sung, W.-K., Zhou, J., Chng, W. J., Li, S., Liu, E., & Tergaonkar, V.
- Affiliations
- Institute of Molecular and Cell Biology (SG)
- Genome Institute of Singapore (SG)
- National University of Singapore (SG)
- Cancer Science Institute of Singapore (SG)
- Corresponding author
- Tergaonkar, Vinay
- ORCID
- Venue
- Nature Cell Biology
- Published
- 2012-11-18
- Volume
- 14
- Issue
- 12
- Pages
- 1270-1281
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- OpenAlex
- W2033861401
- Cited by
- 378
- References
- 70
- Citations by year
- 2026: 20 · 2025: 27 · 2024: 27 · 2023: 34 · 2022: 29 · 2021: 30 · 2020: 32 · 2019: 22 · 2018: 28 · 2017: 19 · 2016: 33 · 2015: 48 · 2014: 15 · 2013: 14
- FWCI
- 16.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- National University of Singapore (submittedVersion)
- Funders
- Agency for Science, Technology and Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Keywords
- telomerase, NF-κB, NF-κB p65, transcriptional regulation, telomere elongation, chronic inflammation, tumor progression, interleukin-6, TNF-α, feedforward control, telomerase reactivation, tumor inflammation
- MeSH terms
- Animals, Female, Humans, Male, Promoter Regions, Genetic, Transcription, Genetic, Tumor Cells, Cultured, Tumor Necrosis Factor-alpha, Signal Transduction, Interleukin-6, NF-kappa B, Telomerase, Cell Line, Tumor, 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