Role of Rb Family in the Epigenetic Definition of Chromatin
Open accessAbstract
Epigenetic changes can influence a variety of cellular processes from regulation of gene transcription to proper chromosome segregation. The molecular activities that dictate the assembly, maintenance and regulation of chromatin structure are beginning to be identified. A recent study demonstrates that the Rb family of tumor suppressors plays a major role in global chromatin structure. In addition to the well-known function of Rb family inducing a repressive chromatin state around euchromatic promoters, Rb proteins have a direct role in the assembly of pericentric and telomeric heterochromatin domains. In particular, the Rb family maintains histone 4 lysine 20 tri-methylation (H4K20) at these constitutive heterochromatin domains. Lack of the Rb family results in decreased H4K20 tri-methylation, coincidental with chromosome segregation defects and abnormal telomere elongation, two processes frequently altered in human cancer. Maintenance of heterochromatic domains, such as those of centromeres and telomeres, may represent a novel tumor suppressor function for the Rb family by ensuing genomic stability.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
RB is an adaptor protein that recruits chromatin remodelling enzymes to control specific target genes and modify chromatin structure chromosome-wide.
“Furthermore, RB is also an adaptor protein that recruits chromatin remodelling enzymes to control the expression of specific target genes and to modify chromatin structure at a chromosome-wide level13,14”
From Cellular mechanisms of tumour suppression by the retinoblastoma gene (2008) · cites this paper as [13]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Still being checked.
Research works printed but not linked: 30
- Weinberg RA. The retinoblastoma protein and cell cycle control. Cell 1995; 81:323-30.
- Lipinski MM, Jacks T. The retinoblastoma gene family in differentiation and development. Oncogene 1999; 18:7873-82.
- Classon M, Harlow E. The retinoblastoma tumour suppressor in development and cancer. Nat Rev Cancer 2002; 2:910-7.
- Dyson N. The regulation of E2F by pRB-family proteins. Genes Dev 1998; 12:2245-62.
- Nevins JR. The Rb/E2F pathway and cancer. Hum Mol Genet 2001; 10:699-703.
- Luo RX, Postigo AA, Dean DC. Rb interacts with histone deacetylase to repress transcrip- tion. Cell 1998; 92:463-73.
- Robertson KD, Ait-Si-Ali S, Yokochi T, Wade PA, Jones PL, Wolffe AP. DNMT1 forms a complex with Rb, E2F1 and HDAC1 and represses transcription from E2F-responsive pro- moters. Nat Genet 2000; 25:338-42.
- Dunaief JL, Strober BE, Guha S, Khavari PA, Alin K, Luban J, Begemann M, Crabtree GR, Goff SP. The retinoblastoma protein and BRG1 form a complex and cooperate to induce cell cycle arrest. Cell 1994; 79:119-30.
- Nielsen SJ, Schneider R, Bauer UM, Bannister AJ, Morrison A, O'Carroll D, Firestein R, Cleary M, Jenuwein T, Herrera RE, Kouzarides T. Rb targets histone H3 methylation and HP1 to promoters. Nature 2001; 412:561-5.
- Vandel L, Nicolas E, Vaute O, Ferreira R, Ait-Si-Ali S, Trouche D. Transcriptional repres- sion by the retinoblastoma protein through the recruitment of a histone methyltransferase. Mol Cell Biol 2001; 21:6484-94.
- Weintraub SJ, Chow KN, Luo RX, Zhang SH, He S, Dean DC. Mechanism of active tran- scriptional repression by the retinoblastoma protein. Nature 1995; 375:812-5.
- Brehm A, Kouzarides T. Retinoblastoma protein meets chromatin. Trends Biochem Sci 1999; 24:142-5.
- Harbour JW, Dean DC. The Rb/E2F pathway: Expanding roles and emerging paradigms. Genes Dev 2000; 14:2393-409.
- Harbour JW, Dean DC. Chromatin remodeling and Rb activity. Curr Opin Cell Biol 2000; 12:685-9.
- Narita M, Nunez S, Heard E, Narita M, Lin AW, Hearn SA, Spector DL, Hannon GJ, Lowe SW. Rb-mediated heterochromatin formation and silencing of E2F target genes dur- ing cellular senescence. Cell 2003; 113:703-16.
- Melcher M, Schmid M, Aagaard L, Selenko P, Laible G, Jenuwein T. Structurefunction analysis of SUV39H1 reveals a dominant role in heterochromatin organization, chromo- some segregation, and mitotic progression. Mol Cell Biol 2000; 20:3728-41.
- Nakayama J, Rice JC, Strahl BD, Allis CD, Grewal SI. Role of histone H3 lysine 9 methy- lation in epigenetic control of heterochromatin assembly. Science 2001; 292:110-3.
- Lachner M, O'Carroll D, Rea S, Mechtler K, Jenuwein T. Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins. Nature 2001; 410:116-20.
- Bannister AJ, Zegerman P, Partridge JF, Miska EA, Thomas JO, Allshire RC, Kouzarides T. Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain. Nature 2001; 410:120-4.
- Lachner M, O'Sullivan RJ, Jenuwein T. An epigenetic road map for histone lysine methy- lation. J Cell Sci 2003; 116:2117-24.
- Schotta G, Lachner M, Sarma K, Ebert A, Sengupta R, Reuter G, Reinberg D, Jenuwein T. A silencing pathway to induce H3-K9 and H4-K20 trimethylation at constitutive hete- rochromatin. Genes Dev 2004; 18:1251-62.
- Lehnertz B, Ueda Y, Derijck AA, Braunschweig U, Perez-Burgos L, Kubicek S, Chen T, Li E, Jenuwein T, Peters AH. Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin. Curr Biol 2003; 13:1192-200.
- Garcia-Cao M, O'Sullivan R, Peters AH, Jenuwein T, Blasco MA. Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltrans- ferases. Nat Genet 2004; 36:94-99.
- Peters AH, O'Carroll D, Scherthan H, Mechtler K, Sauer S, Schofer C, Weipoltshammer K, Pagani M, Lachner M, Kohlmaier A, Opravil S, Doyle M, Sibilia M, Jenuwein T. Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability. Cell 2001; 107:323-37.
- Aagaard L, Schmid M, Warburton P, Jenuwein T. Mitotic phosphorylation of SUV39H1, a novel component of active centromeres, coincides with transient accumulation at mam- malian centromeres. J Cell Sci 2000; 113:817-29.
- Gonzalo S, Garcia-Cao M, Fraga MF, Schotta G, Peters AH, Cotter SE, Eguia R, Dean DC, Esteller M, Jenuwein T, Blasco MA. Role of the RB1 family in stabilizing histone methylation at constitutive heterochromatin. Nat Cell Biol 2005; 7:420-8.
- Garcia-Cao M, Gonzalo S, Dean D, Blasco MA. A role for the Rb family of proteins in controlling telomere length. Nat Genet 2002; 32:415-9.
- Zheng L, Lee WH. Retinoblastoma tumor suppressor and genome stability. Adv Cancer Res 2002; 85:13-50.
- Rowland BD, Denissov SG, Douma S, Stunnenberg HG, Bernards R, Peeper DS. E2F transcriptional repressor complexes are critical downstream targets of p19(ARF)/p53- induced proliferative arrest. Cancer Cell 2002; 2:55-65.
- Fraga MF, Ballestar E, Villar-Garea A, Boix-Chornet M, Espada J, Schotta G, Bonaldi T, Haydon C, Ropero S, Petrie K, Iyer NG, Perez-Rosado A, Calvo E, Lopez JA, Cano A, Calasanz MJ, Colomer D, Piris MA, Ahn N, Imhof A, Caldas C, Jenuwein T, Esteller M. Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hall- mark of human cancer. Nat Genet 2005; 37:391-400.
Cited by
Sorted by citations
Grewal, S. I. S., & Jia, S. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2008 · Cited by 1,263 · see citing works
Cellular mechanisms of tumour suppression by the retinoblastoma gene
Burkhart, D. L., & Sage, J. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2399 · Cited by 974 · see citing works
Histones: annotating chromatin
Campos, E. I., & Reinberg, D. (2009) · Annual Review of Genetics · doi:10.1146/annurev.genet.032608.103928 · Cited by 852 · see citing works
DNA methyltransferases control telomere length and telomere recombination in mammalian cells
Gonzalo, S., Jaco, I., Fraga, M. F., Chen, T., Li, E., Esteller, M., & Blasco, M. A. (2006) · Nature Cell Biology · doi:10.1038/ncb1386 · Cited by 604 · see citing works
Self-citationHutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations
Gonzalo, S., Kreienkamp, R., & Askjaer, P. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2016.06.007 · Cited by 324 · see citing works
Self-citationSwanson, E. C., Manning, B., Zhang, H., & Lawrence, J. B. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201306073 · Cited by 251 · see citing works
“In this context, it is interesting to note that the cell cycle regulator Rb has been reported to interact with the nuclear lamina and play a role in the stabilization of satellite heterochromatin (Gonzalo and Blasco, 2005; Dorner et al., 2007; Marji et al., 2010).”
Novel roles for A‐type lamins in telomere biology and the DNA damage response pathway
González-Suárez, I., Redwood, A. B., Perkins, S. M., Vermolen, B. J., Lichtensztejin, D., Grotsky, D. A., Morgado-Palacin, L., Gapud, E. J., Sleckman, B. P., Sullivan, T. L., et al. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.196 · Cited by 259 · see citing works
Self-citationEpigenetic alterations in aging
Gonzalo, S. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00238.2010 · Cited by 249 · see citing works
Self-citationSequence, Chromatin and Evolution of Satellite DNA
Thakur, J., Packiaraj, J., & Henikoff, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094309 · Cited by 223 · see citing works
A ‘higher order’ of telomere regulation: telomere heterochromatin and telomeric RNAs
Schoeftner, S., & Blasco, M. A. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.197 · Cited by 214 · see citing works
Self-citationEpigenetic mechanisms as a new approach in cancer treatment: An updated review
Fardi, M., Solali, S., & Hagh, M. F. (2018) · Genes & Diseases · doi:10.1016/j.gendis.2018.06.003 · Cited by 211 · see citing works
DNA Methylation: a form of epigenetic control of gene expression
Lim, D. H. K., & Maher, E. R. (2010) · The Obstetrician & Gynaecologist · doi:10.1576/toag.12.1.037.27556 · Cited by 155 · see citing works
Protein arginine methyltransferase 5 is essential for growth of lung cancer cells
Gu, Z., Gao, S., Zhang, F., Wang, Z., Ma, W., Davis, R. E., & Wang, Z. (2012) · Biochemical Journal · doi:10.1042/bj20120768 · Cited by 146 · see citing works
Genetics and Epigenetics of Human Retinoblastoma
Benavente, C. A., & Dyer, M. A. (2015) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-012414-040259 · Cited by 143 · see citing works
Chromatin mechanisms in genomic imprinting
Kacem, S., & Feil, R. (2009) · Mammalian Genome · doi:10.1007/s00335-009-9223-4 · Cited by 135 · see citing works
Induction of microRNAome deregulation in rat liver by long-term tamoxifen exposure
Pogribny, I. P., Tryndyak, V., Boyko, A., Rodriguez‐Juarez, R., Beland, F. A., & Kovalchuk, O. (2007) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2006.12.006 · Cited by 134 · see citing works
Telomere Maintenance Mechanisms in Cancer
Gaspar, T. B., Sá, A., Lopes, J. M., Sobrinho-Simões, M. A., Soares, P., & Vinagre, J. (2018) · Genes · doi:10.3390/genes9050241 · Cited by 132 · see citing works
Linking Heterochromatin Protein 1 (HP1) to cancer progression
Dialynas, G. K., Vitalini, M. W., & Wallrath, L. L. (2008) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2008.09.007 · Cited by 131 · see citing works
Interplay between Epigenetics and Genetics in Cancer
Choi, J. D., & Lee, J.-S. (2013) · Genomics & Informatics · doi:10.5808/gi.2013.11.4.164 · Cited by 131 · see citing works
Kovalchuk, O., Tryndyak, V., Montgomery, B. A., Boyko, A., Kutanzi, K. R., Zemp, F. J., Warbritton, A. R., Latendresse, J. R., Kovalchuk, I., Beland, F. A., et al. (2007) · Cell Cycle · doi:10.4161/cc.6.16.4549 · Cited by 128 · see citing works
Epigenetic regulation of telomeres in human cancer
Vera, E., Canela, A., Fraga, M. F., Esteller, M., & Blasco, M. A. (2008) · Oncogene · doi:10.1038/onc.2008.289 · Cited by 126 · see citing works
Self-citationThe Retinoblastoma (RB) Tumor Suppressor: Pushing Back against Genome Instability on Multiple Fronts
Vélez-Cruz, R., & Johnson, D. G. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081776 · Cited by 113 · see citing works
Redaelli, S., Bentivegna, A., Foudah, D., Miloso, M., Redondo, J., Riva, G., Baronchelli, S., Dalprà, L., & Tredici, G. (2012) · Stem Cell Research & Therapy · doi:10.1186/scrt138 · Cited by 109 · see citing works
Sullivan, L. L., Boivin, C. D., Mravinac, B., Song, I. Y., & Sullivan, B. A. (2011) · Chromosome Research · doi:10.1007/s10577-011-9208-5 · Cited by 105 · see citing works
Manosalva, I., & González, A. (2010) · Theriogenology · doi:10.1016/j.theriogenology.2010.06.024 · Cited by 104 · see citing works
Hutchinson–Gilford progeria syndrome through the lens of transcription
Prokocimer, M., Barkan, R., & Gruenbaum, Y. (2013) · Aging Cell · doi:10.1111/acel.12070 · Cited by 97 · see citing works
Emerging roles of RB family: New defense mechanisms against tumor progression
Indovina, P., Marcelli, E., Casini, N., Rizzo, V., & Giordano, A. (2012) · Journal of Cellular Physiology · doi:10.1002/jcp.24170 · Cited by 94 · see citing works
Chromatin Structure in Telomere Dynamics
Galati, A., Micheli, E., & Cacchione, S. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00046 · Cited by 89 · see citing works
Chromatin regulation and non-coding RNAs at mammalian telomeres
Schoeftner, S., & Blasco, M. A. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.09.015 · Cited by 87 · see citing works
Self-citationBandyopadhyay, D., Curry, J. L., Lin, Q., Richards, H. W., Chen, D., Hornsby, P. J., Timchenko, N. A., & Medrano, E. E. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00308.x · Cited by 81 · see citing works
Suppression of Genome Instability in pRB-Deficient Cells by Enhancement of Chromosome Cohesion
Manning, A. L., Yazinski, S. A., Nicolay, B., Bryll, A. R., Zou, L., & Dyson, N. J. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.01.032 · Cited by 79 · see citing works
Therapeutic targeting of replicative immortality
Yaswen, P., MacKenzie, K. L., Keith, W. N., Hentosh, P., Rodier, F., Zhu, J., Firestone, G. L., Matheu, A., Carnero, A., Bilsland, A. E., et al. (2015) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2015.03.007 · Cited by 74 · see citing works
Current paradigms in epigenetic anticancer therapeutics and future challenges
Singh, M. P., Kumar, V., Sehrawat, N., Yadav, M. K., Chaudhary, M., Upadhyay, S. K., Kumar, S., Sharma, V., Kumar, S., Dilbaghi, N., et al. (2021) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.03.013 · Cited by 77 · see citing works
Wikman, H., & Kettunen, E. (2006) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.6.4.515 · Cited by 73 · see citing works
PR‐SET7 and SUV4‐20H regulate H4 lysine‐20 methylation at imprinting control regions in the mouse
Pannetier, M., Julien, E., Schotta, G., Tardat, M., Sardet, C., Jenuwein, T., & Feil, R. (2008) · EMBO Reports · doi:10.1038/embor.2008.147 · Cited by 72 · see citing works
Loss of A-type lamins and genomic instability
González-Suárez, I., Redwood, A. B., & Gonzalo, S. (2009) · Cell Cycle · doi:10.4161/cc.8.23.10092 · Cited by 68 · see citing works
Self-citationChromatin organization of gammaherpesvirus latent genomes
Tempera, I., & Lieberman, P. M. (2009) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2009.10.004 · Cited by 63 · see citing works
Telomere dynamics: the influence of folate and DNA methylation
Moores, C. J., Fenech, M. F., & O’Callaghan, N. J. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06101.x · Cited by 60 · see citing works
Telomeric armor: the layers of end protection
Oganesian, L., & Karlseder, J. (2009) · Journal of Cell Science · doi:10.1242/jcs.050567 · Cited by 58 · see citing works
Genetic and Epigenetic Discoveries in Human Retinoblastoma
McEvoy, J. D., & Dyer, M. A. (2015) · Critical Reviews™ in Oncogenesis · doi:10.1615/critrevoncog.2015013711 · Cited by 53 · see citing works
Choi, W., Jeon, B.-N., Yoon, J.-H., Koh, D.-I., Kim, M.-H., Yu, M.-Y., Lee, K., Kim, Y., Kim, K., Hur, S. S., et al. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt359 · Cited by 51 · see citing works
Hennig, A. K., Peng, G.-H., & Chen, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069721 · Cited by 50 · see citing works
González-Suárez, I., & Gonzalo, S. (2010) · Nucleus · doi:10.4161/nucl.1.2.10797 · Cited by 45 · see citing works
Self-citationRB loss promotes aberrant ploidy by deregulating levels and activity of DNA replication factors
Srinivasan, S. V., Mayhew, C. N., Schwemberger, S., Zagorski, W., & Knudsen, E. S. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700542200 · Cited by 42 · see citing works
Gu, Z., Zhang, F., Wang, Z.-Q., Ma, W., Davis, R. E., & Wang, Z. (2012) · Oncogene · doi:10.1038/onc.2012.207 · Cited by 38 · see citing works
Chau, C. M., Deng, Z., Kang, H., & Lieberman, P. M. (2008) · Journal of Virology · doi:10.1128/jvi.01412-07 · Cited by 36 · see citing works
Regulation and function of retinoblastoma-related plant genes
Sabelli, P. A., & Larkins, B. A. (2009) · Plant Science · doi:10.1016/j.plantsci.2009.09.012 · Cited by 36 · see citing works
G1 arrest and differentiation can occur independently of Rb family function
Wirt, S. E., Adler, A. S., Gebala, V., Weimann, J. M., Schaffer, B. E., Saddic, L., Viatour, P., Vogel, H. S., Chang, H. Y., Meissner, A., et al. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201003048 · Cited by 35 · see citing works
Brg1 coordinates multiple processes during retinogenesis and is a tumor suppressor in retinoblastoma
Aldiri, I., Ajioka, I., Xu, B.-S., Zhang, J., Chen, X., Benavente, C. A., Finkelstein, D. B., Johnson, D. A., Akiyama, J., Pennacchio, L., et al. (2015) · Development · doi:10.1242/dev.124800 · Cited by 31 · see citing works
The link among microbiota, epigenetics, and disease development
El-Sayed, A., Aleya, L., & Kamel, M. S. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-13862-1 · Cited by 36 · see citing works
RB's original CIN?: Figure 1.Preprint
Sage, J., & Straight, A. F. (2010) · Genes & Development · doi:10.1101/gad.1948010 · Cited by 34 · see citing works
Therapeutic Strategies for RB1-Deficient Cancers: Intersecting Gene Regulation and Targeted Therapy
Huang, M.-F., Wang, Y., Chou, Y., & Lee, D. (2024) · Cancers · doi:10.3390/cancers16081558 · Cited by 32 · see citing works
Alternative lengthening of telomeres (ALT) and chromatin: Is there a connection?
Nittis, T., Guittat, L., & Stewart, S. A. (2007) · Biochimie · doi:10.1016/j.biochi.2007.08.009 · Cited by 33 · see citing works
Epigenetic regulation of cardiac myocyte differentiation†
Oyama, K., El‐Nachef, D., Zhang, Y., Sdek, P., & MacLellan, W. R. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00375 · Cited by 33 · see citing works
Dan, J., Yang, J., Liu, Y., Xiao, A., & Liu, L. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.24980 · Cited by 30 · see citing works
Targeting Notch signaling as a novel therapy for retinoblastoma
Asnaghi, L., Tripathy, A., Yang, Q., Kaur, H., Hanaford, A. R., Yu, W., & Eberhart, C. G. (2016) · Oncotarget · doi:10.18632/oncotarget.12142 · Cited by 30 · see citing works
Bellacchio, E., & Paggi, M. G. (2012) · Journal of Cellular Physiology · doi:10.1002/jcp.24137 · Cited by 29 · see citing works
MBTD1 is associated with Pr-Set7 to stabilize H4K20me1 in mouse oocyte meiotic maturation
Luo, Y.-B., Ma, J.-Y., Zhang, Q.-H., Lin, F., Wang, Z.-W., Huang, L., Schatten, H., & Sun, Q. (2013) · Cell Cycle · doi:10.4161/cc.24216 · Cited by 29 · see citing works
TERRA: Long Noncoding RNA at Eukaryotic Telomeres
Arora, R., Brun, C. M., & Azzalin, C. M. (2010) · Progress in molecular and subcellular biology · doi:10.1007/978-3-642-16502-3_4 · Cited by 27 · see citing works
Lamin A Δexon9 mutation leads to telomere and chromatin defects but not genomic instability
Das, A., Grotsky, D. A., Neumann, M. A., Kreienkamp, R. J., González-Suárez, I., Redwood, A. B., Kennedy, B. K., Stewart, C. L., & Gonzalo, S. (2013) · Nucleus · doi:10.4161/nucl.26873 · Cited by 27 · see citing works
Self-citationBhattacharjee, P., Das, A., Giri, A. K., & Bhattacharjee, P. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.135388 · Cited by 27 · see citing works
Fiorentino, F. P., Marchesi, I., & Giordano, A. (2012) · Journal of Cellular Physiology · doi:10.1002/jcp.24141 · Cited by 27 · see citing works
Optogenetic regulation of site-specific subtelomeric DNA-methylation
Choudhury, S. R., Cui, Y., Narayanan, A., Gilley, D. P., Huda, N., Lo, C., Zhou, F., Yernool, D., & Irudayaraj, J. (2016) · Oncotarget · doi:10.18632/oncotarget.10394 · Cited by 24 · see citing works
Epigenetic regulation of retinal development and disease
Rao, R. C., Hennig, A. K., Malik, M. T. A., Chen, D. F., & Chen, S. (2011) · Journal of ocular biology, diseases, and informatics · doi:10.1007/s12177-012-9083-0 · Cited by 22 · see citing works
Defective Artemis causes mild telomere dysfunction
Yasaei, H., & Slijepčević, P. (2010) · Genome Integrity · doi:10.1186/2041-9414-1-3 · Cited by 22 · see citing works
Chromatin organization changes during the establishment and maintenance of the postmitotic state
Ma, Y., & Buttitta, L. (2017) · Epigenetics & Chromatin · doi:10.1186/s13072-017-0159-8 · Cited by 22 · see citing works
RB and Lamins in Cell Cycle Regulation and Aging
Kennedy, B. K., & Pennypacker, J. K. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-8032-8_6 · Cited by 22 · see citing works
Bikkul, M. U., Faragher, R., Worthington, G. L., Meinke, P., Kerr, A. R. W., Aakila, S., Riyahi, K., Horton, D., Schirmer, E. C., Hubank, M. J. F., et al. (2018) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22711 · Cited by 20 · see citing works
Targeting the epigenome with advanced delivery strategies for epigenetic modulators
Guha, S., Jagadeesan, Y., Pandey, M. M., Mittal, A., & Chitkara, D. (2024) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10710 · Cited by 19 · see citing works
Epigenetic Regulation of Telomere Chromatin Integrity in Pluripotent Embryonic Stem Cells
Wong, L. H. (2010) · Epigenomics · doi:10.2217/epi.10.49 · Cited by 19 · see citing works
The new frontier in cancer research: Deciphering cancer epigenetics
Lohrum, M. A. E., Stunnenberg, H. G., & Logie, C. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2007.03.011 · Cited by 19 · see citing works
The Role of Sumoylation in Senescence
Scurr, L. L., Haferkamp, S., & Rizos, H. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-50044-7_13 · Cited by 18 · see citing works
Yang, Q., Tripathy, A., Yu, W., Eberhart, C. G., & Asnaghi, L. (2017) · Experimental Eye Research · doi:10.1016/j.exer.2017.07.001 · Cited by 15 · see citing works
Epigenetics in Ocular Medicine
Oliver, V. F., van Bysterveldt, K. A., & Merbs, S. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803239-8.00022-3 · Cited by 11 · see citing works
González-Suárez, I., & Gonzalo, S. (2010) · Nucleus · doi:10.4161/nucl.10797 · Cited by 11 · see citing works
Self-citationZluhan‐Martínez, E., Pérez‐Koldenkova, V., Ponce-Castañeda, M. V., Sánchez, M. D. L. P., García‐Ponce, B., Miguel-Hernández, S., Alvarez-Buylla, E. R., & Garay‐Arroyo, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144925 · Cited by 10 · see citing works
RB loss sensitizes cells to replication-associated DNA damage after PARP inhibition by trapping
Zamalloa, L. G., Pruitt, M., Hermance, N. M., Gali, H., Flynn, R. L., & Manning, A. L. (2023) · Life Science Alliance · doi:10.26508/lsa.202302067 · Cited by 10 · see citing works
Crosstalk between chromatin structure, nuclear compartmentalization, and telomere biology
González-Suárez, I., & Gonzalo, S. (2008) · Cytogenetic and Genome Research · doi:10.1159/000167805 · Cited by 10 · see citing works
Self-citationSilvestre, D. C., & Londoño‐Vallejo, A. (2012) · Genome dynamics · doi:10.1159/000337128 · Cited by 10 · see citing works
Brain cancer genomics and epigenomics
Archer, T. C., Sengupta, S., & Pomeroy, S. L. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64076-5.00050-8 · Cited by 10 · see citing works
Skin Tumors Rb(eing) Uncovered
Costa, C., Paramio, J. M., & Santos, M. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00307 · Cited by 8 · see citing works
History and Genetics of Retinoblastoma
Alzahem, T. A., Alsarhani, W. K., Albahlal, A. A., Abu‐Safieh, L., & Al-Dahmash, S. A. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.89035 · Cited by 7 · see citing works
Human Diseases Associated With Genome Instability
Feltes, B. C., Poloni, J. D. F., Miyamoto, K. N., & Bonatto, D. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00026-4 · Cited by 6 · see citing works
Retinoblastoma protein regulates carcinogen susceptibility at heterochromatic cancer driver loci
Wong, K. M., King, D. A., Schwartz, E. K., Herrera, R. E., & Morrison, A. J. (2022) · Life Science Alliance · doi:10.26508/lsa.202101134 · Cited by 7 · see citing works
Mouse oocyte meiosis is disturbed by knockdown of Suv4-20h
Xiong, K., Wu, W., Wang, X., Ma, X., Chen, J., & Liu, H. (2012) · Reproduction Fertility and Development · doi:10.1071/rd12116 · Cited by 6 · see citing works
Kuijpers, T., Kleinjans, J. C. S., & Jennen, D. G. J. (2021) · Scientific Reports · doi:10.1038/s41598-021-90047-3 · Cited by 5 · see citing works
Molecular Genetics and Cancer Biology
Gonzalgo, M. L., & Meeker, A. K. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4160-6911-9.00018-9 · Cited by 5 · see citing works
Epigenetics and the role of nutraceuticals in health and disease
El-Sayed, A., Aleya, L., & Kamel, M. S. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-25236-w · Cited by 5 · see citing works
Dysfunction of the RB Retinoblastoma Gene in Cancer
Pentimalli, F., Cito, L., & Giordano, A. (2009) · Humana Press eBooks · doi:10.1007/978-1-60761-178-3_8 · Cited by 5 · see citing works
FAM111A Is a Novel Molecular Marker for Oocyte Aging
Yang, H., Kolben, T., Kessler, M., Meister, S., Paul, C., van Dorp, J., Eren, S., Kühn, C., Rahmeh, M., Herbst, C., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10020257 · Cited by 3 · see citing works
RB loss sensitizes cells to replication-associated DNA damage by PARP inhibitionPreprint
Zamalloa, L. G., Pruitt, M., Hermance, N. M., Gali, H., Flynn, R. L., & Manning, A. L. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.25.532215 · Cited by 3 · see citing works
RB regulation of developmental transcriptional programs
Dimova, D. K. (2011) · Fly · doi:10.4161/fly.5.2.14187 · Cited by 2 · see citing works
Swanson, E. C. (2014) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/m2k30f · Cited by 1 · see citing works
Epigenetic Mechanisms of Retinal Disease
He, S., Yiu, G. C., Zhou, P., & Chen, D. F. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4557-0737-9.00033-3 · Cited by 1 · see citing works
RB dependent transcriptional regulation at mitotic centromeres preserves genome stability
Crowley, E. A., & Manning, A. L. (2025) · Life Science Alliance · doi:10.26508/lsa.202503433 · Cited by 1 · see citing works
Zhang, L., Song, W., Wang, J., Zhao, Y., Yuan, C., Ruan, Z., Chen, J., Zhao, J., Yao, H., Chen, H., et al. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108098 · Cited by 1 · see citing works
Telomere Biology and Biochemistry
Gardano, L., & Harrington, L. A. (2009) · Springer eBooks · doi:10.1007/978-1-4419-1075-2_1 · Cited by 1 · see citing works
Chromatin Structure in Senescent Cells
Richards, H. W., & Medrano, E. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1075-2_6 · Cited by 1 · see citing works
The Function and Regulation of Senescent Stromal-Derived Osteopontin
Pazolli, E. (2010) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7x34vgs
CONSTITUTIVE AND SOMATIC GENETIC EVENTS IN RETINOMA AND RETINOBLASTOMA
Sampieri, K. (2008)
- Authors
- Gonzalo, S., & Blasco, M. A.
- Affiliations
- Spanish National Cancer Research Centre (ES)
- ORCID
- Gonzalo, Susana
- Venue
- Cell Cycle
- Publisher
- Informa UK Limited
- Published
- 2005-04-08
- Volume
- 4
- Issue
- 6
- Pages
- 752-755
- ISSN
- 1538-4101 (ISSN-L)
- 1551-4005
- OpenAlex
- W2085216724
- Cited by
- 112
- References
- 0
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 3 · 2023: 3 · 2022: 2 · 2021: 6 · 2020: 1 · 2019: 3 · 2018: 5 · 2017: 4 · 2016: 6 · 2015: 6 · 2014: 4 · 2013: 9 · 2012: 10
- FWCI
- 2.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cell Cycle (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation
- European Commission (LSHC-CT-2003-506803, FOOD-CT-2003-506850)
- Ministerio de Ciencia y Tecnología
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- retinoblastoma protein, chromatin structure, heterochromatin, telomeres, centromere, H4K20 trimethylation, tumor suppressor function, chromosome segregation, telomere elongation, genome stability, transcriptional regulation
- MeSH terms
- Multigene Family, Heterochromatin, Humans, Promoter Regions, Genetic, Retinoblastoma Protein, Chromatin Assembly and Disassembly, Epigenesis, Genetic
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