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Suppression of induced pluripotent stem cell generation by the p53–p21 pathway
Open accessAbstract
Induced pluripotent stem (iPS) cells can be generated from somatic cells by the introduction of Oct3/4 (also known as Pou5f1), Sox2, Klf4 and c-Myc, in mouse and in human. The efficiency of this process, however, is low. Pluripotency can be induced without c-Myc, but with even lower efficiency. A p53 (also known as TP53 in humans and Trp53 in mice) short-interfering RNA (siRNA) was recently shown to promote human iPS cell generation, but the specificity and mechanisms remain to be determined. Here we report that up to 10% of transduced mouse embryonic fibroblasts lacking p53 became iPS cells, even without the Myc retrovirus. The p53 deletion also promoted the induction of integration-free mouse iPS cells with plasmid transfection. Furthermore, in the p53-null background, iPS cells were generated from terminally differentiated T lymphocytes. The suppression of p53 also increased the efficiency of human iPS cell generation. DNA microarray analyses identified 34 p53-regulated genes that are common in mouse and human fibroblasts. Functional analyses of these genes demonstrate that the p53-p21 pathway serves as a barrier not only in tumorigenicity, but also in iPS cell generation.
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“It is known that OSKM induction activates the p53–p21 pathway25.”
From In vivo partial reprogramming of myofibers promotes muscle regeneration by remodeling the stem cell niche (2021) · cites this paper as [25]
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Cites
Takahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673
Self-citationInduction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors
Takahashi, K., Tanabe, K., Ohnuki, M., Narita, M., Ichisaka, T., Tomoda, K., & Yamanaka, S. (2007) · Cell · doi:10.1016/j.cell.2007.11.019 · Cited by 20,221
Self-citationInduced Pluripotent Stem Cell Lines Derived from Human Somatic Cells
Yu, J., Vodyanik, M. A., Smuga-Otto, K., Antosiewicz-Bourget, J., Frane, J. L., Tian, S., Nie, J., Jonsdottir, G. A., Ruotti, V., Stewart, R., et al. (2007) · Science · doi:10.1126/science.1151526 · Cited by 10,310
Generation of germline-competent induced pluripotent stem cells
Okita, K., Ichisaka, T., & Yamanaka, S. (2007) · Nature · doi:10.1038/nature05934 · Cited by 4,438
Self-citationIn vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state
Wernig, M., Meissner, A., Foreman, R. K., Brambrink, T., Ku, M., Hochedlinger, K., Bernstein, B., & Jaenisch, R. (2007) · Nature · doi:10.1038/nature05944 · Cited by 2,732
Reprogramming of human somatic cells to pluripotency with defined factors
Park, I.-H., Zhao, R., West, J. A., Yabuuchi, A., Huo, H., Ince, T. A., Lerou, P. H., Lensch, M. W., & Daley, G. Q. (2008) · Nature · doi:10.1038/nature06534 · Cited by 2,436
Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts
Nakagawa, M., Koyanagi, M., Tanabe, K., Takahashi, K., Ichisaka, T., Aoi, T., Okita, K., Mochiduki, Y., Takizawa, N., & Yamanaka, S. (2008) · Nature Biotechnology · doi:10.1038/nbt1374 · Cited by 2,380
Self-citationGeneration of Mouse Induced Pluripotent Stem Cells Without Viral Vectors
Okita, K., Nakagawa, M., Hong, H., Ichisaka, T., & Yamanaka, S. (2008) · Science · doi:10.1126/science.1164270 · Cited by 2,056
Self-citationMaherali, N., Sridharan, R., Xie, W., Utikal, J., Eminli, S., Arnold, K., Stadtfeld, M., Yachechko, R., Tchieu, J., Jaenisch, R., et al. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.05.014 · Cited by 1,725
Plat-E: an efficient and stable system for transient packaging of retroviruses
MORITA, S., Kojima, T., & Kitamura, T. (2000) · Gene Therapy · doi:10.1038/sj.gt.3301206 · Cited by 1,660
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Mahabadi, J. A., Sabzalipoor, H., Nikzad, H., Seyedhosseini, E., Enderami, S. E., Hayat, S. M. G., & Sahebkar, A. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27990 · Cited by 22
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Chiche, A., Chen, C., & Li, H. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.111005 · Cited by 21
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Kurosaki, H., Hiratsuka, M., Imaoka, N., Iida, Y., Uno, N., Kazuki, Y., Ishihara, C., Yakura, Y., Mimuro, J., Sakata, Y., et al. (2011) · Journal of Human Genetics · doi:10.1038/jhg.2011.88 · Cited by 21
Chang, G., Miao, Y., Zhang, Y., Liu, S., Kou, Z., Ding, J., Chen, D., Sun, Q., & Gao, S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010320 · Cited by 21
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Guo, W., Wang, X., & Wang, Y. (2014) · Protein & Cell · doi:10.1007/s13238-013-0014-z · Cited by 21
Liu, L., Xu, F., Chang, C., He, Q., Wu, L., Zhang, Z., & Li, X. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.526 · Cited by 21
Stępniewski, J., Pacholczak, T., Skrzypczyk, A., Cieśla, M., Szade, A., Szade, K., Bidanel, R., Langrzyk, A., Grochowski, R., Vandermeeren, F., et al. (2018) · IUBMB Life · doi:10.1002/iub.1711 · Cited by 21
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Al‐Khalaf, H. H., & Aboussekhra, A. (2018) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-18-0017 · Cited by 22
Xu, Y., Nasri, M., Dannenmann, B., Mir, P., Zahabi, A., Welte, K., Morishima, T., & Skokowa, J. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02144-9 · Cited by 21
Viswabandya, A., Baidya, S., Nair, S. C., Lakshmi, K. M., Mathews, V., George, B., Chandy, M., & Srivastava, A. (2010) · American Journal of Hematology · doi:10.1002/ajh.21741 · Cited by 21
Shared mechanisms in stemness and carcinogenesis: lessons from oncogenic viruses
Iacovides, D. C., Michael, S., Achilleos, C., & Strati, K. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00066 · Cited by 21
Takahashi, K. (2010) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2010.01169.x · Cited by 20
Self-citationMetabostemness in cancer: Linking metaboloepigenetics and mitophagy in remodeling cancer stem cells
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Injury primes mutation-bearing astrocytes for dedifferentiation in later life
Ragdale, H. S., Clements, M., Tang, W., Deltcheva, E. M., Andreassi, C., Lai, A. G., Chang, W. H., Pandrea, M., Andrew, I., Gamé, L., et al. (2023) · Current Biology · doi:10.1016/j.cub.2023.02.013 · Cited by 20
Replication stress in mammalian embryo development, differentiation, and reprogramming
Wang, N., Xu, S., & Egli, D. M. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.03.015 · Cited by 21
Miyoshi, K., Horiguchi, T., Tanimura, A., Hagita, H., & Noma, T. (2015) · BioMed Research International · doi:10.1155/2015/121575 · Cited by 21
Practical Integration‐Free Episomal Methods for Generating Human Induced Pluripotent Stem Cells
Kime, C., Rand, T., Ivey, K. N., Srivastava, D., Yamanaka, S., & Tomoda, K. (2015) · Current Protocols in Human Genetics · doi:10.1002/0471142905.hg2102s87 · Cited by 20
Self-citationInduced Pluripotent Stem Cells: A New Approach for Physiological Research
Pfannkuche, K., Hannes, T., Khalil, M., Noghabi, M. S., Morshedi, A., Hescheler, J., & Dröge, P. (2010) · Cellular Physiology and Biochemistry · doi:10.1159/000320514 · Cited by 21
Therapeutic opportunities: Telomere maintenance in inducible pluripotent stem cells
Gourronc, F. A., & Klingelhutz, A. J. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.05.008 · Cited by 20
Genome integrity: linking pluripotency and tumorgenicity
Deng, W., & Xu, Y. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.09.004 · Cited by 20
Suppression of Lefty expression in induced pluripotent cancer cells
Saito, A. M., Ochiai, H., Okada, S., Miyata, N., & Azuma, T. (2013) · The FASEB Journal · doi:10.1096/fj.12-221432 · Cited by 20
Mahapatra, P. S., Singh, R., Kumar, K., Sahoo, N. R., Agarwal, P., Mili, B., Das, K., Sarkar, M., BHANJA, S. K., Das, B. C., et al. (2016) · The International Journal of Developmental Biology · doi:10.1387/ijdb.160006sb · Cited by 20
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Swaidan, N. T., Salloum‐Asfar, S., Palangi, F., Errafii, K., Soliman, N., Aboughalia, A. T., Saidwali, A. H., Abdulla, S. A., & Emara, M. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-78932-9 · Cited by 20
Xu, H., Zhou, Y., Coughlan, K. A., Ding, Y., Wang, S., Wu, Y., Song, P., & Zou, M. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2014.10.002 · Cited by 21
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Nii, T., Marumoto, T., & Tani, K. (2012) · BioMed Research International · doi:10.1155/2012/903435 · Cited by 21
Lu, X., Wei, Y., & Liu, F. (2015) · Cell Discovery · doi:10.1038/celldisc.2015.27 · Cited by 21
Innovation for hepatotoxicity in vitro research models: A review
Han, W., Wu, Q., Zhang, X., & Duan, Z. (2018) · Journal of Applied Toxicology · doi:10.1002/jat.3711 · Cited by 22
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Zheng, Z. S., Li, C., Ha, P., Chang, G. X., Yang, P., Zhang, X., Kim, J. K., Jiang, W., Pang, X., Berthiaume, E. A., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci125015 · Cited by 20
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Peng, K.-L., Vasudevan, H. N., Lockney, D. T., Baum, R., Hendrickson, R. C., Raleigh, D. R., & Schmitt, A. M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2203738119 · Cited by 19
Kaemena, D. F., Yoshihara, M., Beniazza, M., Ashmore, J., Zhao, S., Bertenstam, M., Olariu, V., Katayama, S., Okita, K., Tomlinson, S. R., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36097-9 · Cited by 20
Self-citationPossible Strategies to Reduce the Tumorigenic Risk of Reprogrammed Normal and Cancer Cells
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Pietronave, S., & Prat, M. (2012) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y11-125 · Cited by 19
Cao, S., Loh, K. M., Pei, Y., Zhang, W., & Han, J. (2012) · Protein & Cell · doi:10.1007/s13238-012-2078-6 · Cited by 19
Acute reduction in oxygen tension enhances the induction of neurons from human fibroblasts
Davila, J., Chanda, S., Ang, C. E., Südhof, T. C., & Wernig, M. (2013) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2013.03.020 · Cited by 19
Informational needs assessment of non‐Hodgkin lymphoma survivors and their physicians
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Weige, C. C., Birtwistle, M. R., Mallick, H., Yi, N., Berrong, Z., Cloessner, E., Duff, K., Tidwell, J. A., Clendenning, M., Wilkerson, B. J., et al. (2014) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-13-0286-t · Cited by 19
Zhong, L., Mu, H., Wen, B., Zhang, W., Wei, Q., Gao, G., Han, J., & Cao, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-24863-5 · Cited by 19
Chen, J., Ouyang, H., An, X., & Liu, S. (2018) · Oncology Letters · doi:10.3892/ol.2018.9587 · Cited by 19
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Mellis, I. A., Edelstein, H. I., Truitt, R., Goyal, Y., Beck, L. E., Symmons, O., Dunagin, M. C., Linares-Saldana, R., Shah, P. P., Pérez-Bermejo, J. A., et al. (2021) · Cell Systems · doi:10.1016/j.cels.2021.07.003 · Cited by 20
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Hlavová, M., Čížková, M., Vítová, M., Bišová, K., & Zachleder, V. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019626 · Cited by 19
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Is aging a barrier to reprogramming? Lessons from induced pluripotent stem cells
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Bertoldo, M. J., Locatelli, Y., O’Neill, C., & Mermillod, P. (2014) · Reproduction Fertility and Development · doi:10.1071/rd14049 · Cited by 19
Shimizu, M., Shibuya, H., & Tanaka, N. (2022) · Scientific Reports · doi:10.1038/s41598-022-06916-y · Cited by 18
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The role of p53 in limiting somatic cell reprogramming
Liu, Y., Hoya-Arias, R., & Nimer, S. D. (2009) · Cell Research · doi:10.1038/cr.2009.121 · Cited by 18
Liu, J., Sümer, H., Leung, J., Upton, K. R., Dottori, M., Pébay, A., & Verma, P. J. (2010) · Cell Transplantation · doi:10.3727/096368910x514305 · Cited by 18
Jincho, Y., Araki, R., Hoki, Y., Tamura, C., Nakamura, M., Ando, S., Kasama, Y., & Abe, M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.115915 · Cited by 18
Technological Progress in Generation of Induced Pluripotent Stem Cells for Clinical Applications
Oh, S.-I., Lee, C. K., Cho, K. J., Lee, K.-O., Cho, S., & Hong, S. (2012) · The Scientific World JOURNAL · doi:10.1100/2012/417809 · Cited by 18
Li, J., Yu, T., Xia, Z., Chen, G.-C., Yuan, Y., Zhong, W., Zhao, L., & Chen, Q. (2014) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2014.05.001 · Cited by 19
Role of Rho kinases in abnormal and normal hematopoiesis
Mali, R. S., Kapur, S., & Kapur, R. (2014) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000056 · Cited by 18
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Differential regulated microRNA by wild type and mutant p53 in induced pluripotent stem cells
Grespi, F., Landré, V., Molchadsky, A., Daniele, N. D., Marsella, L., Melino, G., & Rotter, V. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.419 · Cited by 18
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Watanabe, T., Yamazaki, S., Yoneda, N., Shinohara, H., Tomioka, I., Higuchi, Y., Yagoto, M., Ema, M., Suemizu, H., Kawai, K., et al. (2019) · Genes to Cells · doi:10.1111/gtc.12702 · Cited by 19
Allen, J. E., Hart, L. S., Dicker, D. T., Wang, W., & El‐Deiry, W. S. (2009) · Cancer Biology & Therapy · doi:10.4161/cbt.8.22.10450 · Cited by 18
The H2B ubiquitin-protein ligase RNF40 is required for somatic cell reprogramming
Xie, W., Miehe, M., Laufer, S. D., & Johnsen, S. A. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2482-4 · Cited by 19
Reprogramming and transdifferentiation - two key processes for regenerative medicine
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The Cell Biology of Stem Cells
Meshorer, E., & Plath, K. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7037-4 · Cited by 20
Rehman, A., Fatima, I., Noor, F., Qasim, M., Wang, P., jia, J., Alshabrmi, F. M., & Liao, M. (2024) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2024.108661 · Cited by 17
Concise Review: Induced Pluripotency by Defined Factors: Prey of Oxidative Stress
Qi, S., Fang, Z. H., Wang, D., Menéndez, P. R., Yao, K., & Ji, J. (2015) · Stem Cells · doi:10.1002/stem.1946 · Cited by 17
Yan, X., Lv, A., Xing, Y., Liu, B., Hou, J., Huang, W. C., & Li, Y. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-011-0801-x · Cited by 17
Iglesias, J. M., Leis, O., Ruiz, E. P., Barrie, J. G., Garcia‐García, F., Aduriz, A., Beloqui, I., Hernández-García, S., Lopez-Mato, M. P., Dopazo, J., et al. (2014) · Frontiers in Oncology · doi:10.3389/fonc.2014.00308 · Cited by 18
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Chistiakov, D. A., & Chistiakov, P. A. (2011) · Hepatology Research · doi:10.1111/j.1872-034x.2011.00896.x · Cited by 17
Fujii, Y. R. (2010) · The Open Virology Journal · doi:10.2174/1874357901004010063 · Cited by 18
TRIM32 modulates pluripotency entry and exit by directly regulating Oct4 stability
Bahnassawy, L., Perumal, T. M., González-Cano, L., Hillje, A., Taher, L., Makałowski, W., Suzuki, Y., Fuellen, G., del Sol, A., & Schwamborn, J. C. (2015) · Scientific Reports · doi:10.1038/srep13456 · Cited by 17
Safe Transplantation Of Pluripotent Stem Cell By Preventing Teratoma Formation
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Epigenetics of Solid Cancer Stem Cells
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Sogabe, Y., Seno, H., Yamamoto, T., & Yamada, Y. (2018) · Cancer Science · doi:10.1111/cas.13731 · Cited by 17
RNA-Based Strategies for Cell Reprogramming toward Pluripotency
Bailly, A., Milhavet, O., & Lemaı̂tre, J.-M. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14020317 · Cited by 18
Mettl14-driven senescence-associated secretory phenotype facilitates somatic cell reprogramming
Xi, C., Sun, J., Xu, X., Wu, Y., Kou, X., Zhao, Y., Shen, J., Dong, Y., Chen, K., Su, Z., et al. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.06.012 · Cited by 17
Molecular mechanisms of pluripotency and reprogramming
Na, J., Plews, J. R., Li, J., Wongtrakoongate, P., Tuuri, T., Féki, A., Andrews, P. W., & Unger, C. A. (2010) · Stem Cell Research & Therapy · doi:10.1186/scrt33 · Cited by 18
Induced pluripotent stem cells – alchemist's tale or clinical reality?
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Metadata
- Authors
- Hong, H., Takahashi, K., Ichisaka, T., Aoi, T., Kanagawa, O., Nakagawa, M., Okita, K., & Yamanaka, S.
- Affiliations
- Kyoto University (JP)
- RIKEN (JP)
- Gladstone Institutes (US)
- Corresponding author
- Yamanaka, Shinya
- Venue
- Nature
- Published
- 2009-08
- Volume
- 460
- Issue
- 7259
- Pages
- 1132-1135
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2917235
- OpenAlex
- W2081620485
- Cited by
- 1,301
- References
- 23
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 25 · 2023: 29 · 2022: 44 · 2021: 51 · 2020: 41 · 2019: 56 · 2018: 63 · 2017: 59 · 2016: 78 · 2015: 88 · 2014: 116 · 2013: 117 · 2012: 168
- FWCI
- 67.71
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Kyoto University Research Information Repository (Kyoto University) (submittedVersion)
- Funders
- National Heart, Lung, and Blood Institute (U01HL100406)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- induced pluripotent stem cells, p53, p21, p53/p21 pathway, reprogramming efficiency, mouse embryonic fibroblasts, T cells, plasmid transfection, p53 target genes, tumorigenicity, Oct4, SOX2, KLF4, c-Myc
- MeSH terms
- Kruppel-Like Factor 4, Adult, Animals, Cell Differentiation, Embryo, Mammalian, Female, Fibroblasts, Humans, Male, Plasmids, T-Lymphocytes, Transfection, Tumor Suppressor Protein p53, Genes, myc, Oligonucleotide Array Sequence Analysis, Gene Silencing, Gene Expression Profiling, Pluripotent Stem Cells, Cyclin-Dependent Kinase Inhibitor p21, Mice
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