Characterization of MAD2B and Other Mitotic Spindle Checkpoint Genes
Open accessAbstract
Aneuploidy is a characteristic of the majority of human cancers, and recent work has suggested that mitotic checkpoint defects play a role in its development. To further explore this issue, we isolated a novel human gene, MAD2B (MAD2L2), which is homologous to the spindle checkpoint gene MAD2 (MAD2L1). We determined the chromosomal localization of it and other spindle checkpoint genes, including MAD1L1, MAD2, BUB3, TTK (MPS1L1), and CDC20. In addition, we resolved the genomic intron-exon structure of the human BUB1 gene. We then searched for mutations in these genes in a panel of 19 aneuploid colorectal tumors. No new mutations were identified, suggesting that genes yet to be discovered are responsible for most of the checkpoint defects observed in aneuploid cancers.
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The results provide one explanation for why loss-of-function mutations in spindle checkpoint genes are uncommon in human cancers.
“Hence, our results provide one explanation for why loss-of-function mutations in spindle checkpoint genes are uncommon in human cancers 11,12 .”
From Rb inactivation promotes genomic instability by uncoupling cell cycle progression from mitotic control (2004) · cites this paper as [11]
Loss-of-function mutations in spindle checkpoint genes are rarely observed in human tumours.
“loss-of-function mutations in spindle checkpoint genes are rarely observed in human tumours 11,12 .”
From Rb inactivation promotes genomic instability by uncoupling cell cycle progression from mitotic control (2004) · cites this paper as [11]
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Cites
Genetic instabilities in human cancers
Lengauer, C., Kinzler, K. W., & Vogelstein, B. (1998) · Nature · doi:10.1038/25292 · Cited by 4,168 · see citing works
Self-citationGenetic instability in colorectal cancers
Lengauer, C., Kinzler, K. W., & Vogelstein, B. (1997) · Nature · doi:10.1038/386623a0 · Cited by 1,995 · see citing works
Self-citationMutations of mitotic checkpoint genes in human cancers
Cahill, D. P., Christoph Lengauer, C., Yu, J., Riggins, G. J., Willson, J. K. V., Markowitz, S. D., Kinzler, K. W., & Vogelstein, B. (1998) · Nature · doi:10.1038/32688 · Cited by 1,485 · see citing works
Self-citation(1991) · PubMed · Cited by 1,305 · see citing works
Feedback control of mitosis in budding yeast
Li, R., & Murray, A. W. (1991) · Cell · doi:10.1016/0092-8674(81)90015-5 · Cited by 1,174 · see citing works
S. cerevisiae genes required for cell cycle arrest in response to loss of microtubule function
Hoyt, M. A., Totis, L., & Roberts, B. T. (1991) · Cell · doi:10.1016/0092-8674(81)90014-3 · Cited by 1,138 · see citing works
Zur Frage der Entstehung maligner Tumoren
Boveri, T. (1914) · Cited by 789 · see citing works
Association of Spindle Assembly Checkpoint Component XMAD2 with Unattached Kinetochores
Chen, R., Waters, J. C., Salmon, E. D., & Murray, A. W. (1996) · Science · doi:10.1126/science.274.5285.242 · Cited by 783 · see citing works
Defects in a cell cycle checkpoint may be responsible for the genomic instability of cancer cells
Hartwell, L. H. (1992) · Cell · doi:10.1016/0092-8674(92)90586-2 · Cited by 770 · see citing works
Identification of a Human Mitotic Checkpoint Gene: hsMAD2
Li, Y., & Benezra, R. (1996) · Science · doi:10.1126/science.274.5285.246 · Cited by 597 · see citing works
Fang, G., Yu, H., & Kirschner, M. W. (1998) · Genes & Development · doi:10.1101/gad.12.12.1871 · Cited by 597 · see citing works
Budding Yeast Cdc20: A Target of the Spindle Checkpoint
Hwang, L. H., Lau, L. F., Smith, D. L., Mistrot, C., Hardwick, K., Hwang, E. S., Amon, A., & Murray, A. W. (1998) · Science · doi:10.1126/science.279.5353.1041 · Cited by 567 · see citing works
Taylor, S. S., & McKeon, F. (1997) · Cell · doi:10.1016/s0092-8674(00)80255-x · Cited by 536 · see citing works
Human T Cell Leukemia Virus Type 1 Oncoprotein Tax Targets the Human Mitotic Checkpoint Protein MAD1
Jin, D., Spencer, F. A., & Jeang, K.-T. (1998) · Cell · doi:10.1016/s0092-8674(00)81148-4 · Cited by 520 · see citing works
Taylor, S. S., Ha, E., & McKeon, F. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.1.1 · Cited by 458 · see citing works
Weiss, E., & Winey, M. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.132.1.111 · Cited by 424 · see citing works
Fission Yeast Slp1: An Effector of the Mad2-Dependent Spindle Checkpoint
Kim, S. H., Lin, D. P., Matsumoto, S., Kitazono, A. A., & Matsumoto, T. (1998) · Science · doi:10.1126/science.279.5353.1045 · Cited by 379 · see citing works
Activation of the Budding Yeast Spindle Assembly Checkpoint Without Mitotic Spindle Disruption
Hardwick, K., Weiss, E. L., Luca, F. C., Winey, M., & Murray, A. W. (1996) · Science · doi:10.1126/science.273.5277.953 · Cited by 339 · see citing works
Mismatch repair: mechanisms and relationship to cancer susceptibility
Kolodner, R. D. (1995) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)89087-8 · Cited by 305 · see citing works
Chan, G. K. T., Schaar, B. T., & Yen, T. J. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.1.49 · Cited by 281 · see citing works
Strand-specific Mismatch Repair in Mammalian Cells
Modrich, P. L. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.40.24727 · Cited by 246 · see citing works
Kallio, M. J., Weinstein, J., Daum, J. R., Burke, D. J., & Gorbsky, G. J. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.6.1393 · Cited by 240 · see citing works
He, X., Patterson, T. E., & Sazer, S. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.15.7965 · Cited by 234 · see citing works
Mad1p, a phosphoprotein component of the spindle assembly checkpoint in budding yeast.
Hardwick, K., & Murray, A. W. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.3.709 · Cited by 231 · see citing works
The Saccharomyces cerevisiae checkpoint gene BUB1 encodes a novel protein kinase.
Roberts, B. T., Farr, K. A., & Hoyt, M. A. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.12.8282 · Cited by 227 · see citing works
Cancer of the microsatellite mutator phenotype.
Perucho, M. (1996) · PubMed · Cited by 227 · see citing works
Replication errors: cha(lle)nging the genome
Jiricny, J. (1998) · The EMBO Journal · doi:10.1093/emboj/17.22.6427 · Cited by 202 · see citing works
Expression of TTK, a novel human protein kinase, is associated with cell proliferation.
Mills, G. B., Schmandt, R. E., McGill, M., Amendola, A., Hill, M., Jacobs, K., May, C., Rodricks, A.-M., Campbell, S., & Hogg, D. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)49633-6 · Cited by 136 · see citing works
Hardwick, K. (1998) · Trends in Genetics · doi:10.1016/s0168-9525(97)01340-1 · Cited by 110 · see citing works
Efimov, V. P., & Morris, N. R. (1998) · Genetics · doi:10.1093/genetics/149.1.101 · Cited by 68 · see citing works
Markowitz, S. D., Myeroff, L. L., Cooper, M. J., Traicoff, J. L., Kochera, M., Lutterbaugh, J., Swiriduk, M., & Willson, J. K. V. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117048 · Cited by 65 · see citing works
Dominant Alleles of Saccharomyces cerevisiae CDC20 Reveal Its Role in Promoting Anaphase
Schott, E. J., & Hoyt, M. A. (1998) · Genetics · doi:10.1093/genetics/148.2.599 · Cited by 52 · see citing works
Mammalian BUB1 Protein Kinases: Map Positions andin VivoExpression
Pangilinan, F., Li, Q., Weaver, T., Lewis, B. C., Dang, C. V., & Spencer, F. A. (1997) · Genomics · doi:10.1006/geno.1997.5068 · Cited by 43 · see citing works
Li, X., Deng, H., Yang, Y., Jia Hui, X. I. A., Hung, W.-Y., & Siddque, T. (2008) · Cytogenetics and Cell Genetics · doi:10.1159/000134631 · Cited by 22 · see citing works
Map Location and Gene Structure of theHomo sapiensMitotic Arrest Deficient 2 (MAD2L1) Gene at 4q27
Krishnan, R., Goodman, B. K., Jin, D., Jeang, K.-T., Collins, C. S., Stetten, G., & Spencer, F. A. (1998) · Genomics · doi:10.1006/geno.1998.5233 · Cited by 16 · see citing works
Flagged first, then by citations
1 of the 36 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
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 · see citing works
Mitotic kinases as regulators of cell division and its checkpoints
Nigg, E. A. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35048096 · Cited by 1,541 · see citing works
Genetic Pathways to Primary and Secondary Glioblastoma
Ohgaki, H., & Kleihues, P. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.070011 · Cited by 1,487 · see citing works
On the road to cancer: aneuploidy and the mitotic checkpoint
Kops, G. J. P. L., Weaver, B. A. A., & Cleveland, D. W. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1714 · Cited by 1,188 · see citing works
Causes and consequences of aneuploidy in cancer
Gordon, D. J., Resio, B. J., & Pellman, D. S. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3123 · Cited by 818 · see citing works
MAD2 haplo-insufficiency causes premature anaphase and chromosome instability in mammalian cells
Michel, L. S., Liberal, V., Chatterjee, A., Kirchwegger, R., Pasche, B., Gerald, W. L., Dobles, M., Sorger, P. K., Murty, V. V. V. S., & Benezra, R. (2001) · Nature · doi:10.1038/35053094 · Cited by 725 · see citing works
Anand, S., Penrhyn-Lowe, S., & Venkitaraman, A. R. (2003) · Cancer Cell · doi:10.1016/s1535-6108(02)00235-0 · Cited by 631 · see citing works
Hernando, E., Nahlé, Z., Juan, G., Diaz-Rodriguez, E., Alaminos, M., Hemann, M., Michel, L., Mittal, V., Gerald, W., Benezra, R., et al. (2004) · Nature · doi:10.1038/nature02820 · Cited by 562 · see citing works
Short- and long-term effects of chromosome mis-segregation and aneuploidy
Santaguida, S., & Amon, A. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4025 · Cited by 535 · see citing works
The anaphase-promoting complex: it's not just for mitosis any morePreprint
Harper, J. W., Burton, J. L., & Solomon, M. J. (2002) · Genes & Development · doi:10.1101/gad.1013102 · Cited by 490 · see citing works
Significance of multiple mutations in cancer
Loeb, K. R., & Loeb, L. A. (2000) · Carcinogenesis · doi:10.1093/carcin/21.3.379 · Cited by 460 · see citing works
Chfr defines a mitotic stress checkpoint that delays entry into metaphase
Scolnick, D. M., & Halazonetis, T. D. (2000) · Nature · doi:10.1038/35019108 · Cited by 375 · see citing works
Genomic instability and colon cancer
Grady, W. M. (2003) · Cancer and Metastasis Reviews · doi:10.1023/a:1025861527711 · Cited by 348 · see citing works
Babu, J. R., Jeganathan, K. B., Baker, D. J., Wu, X., Kang, N., & van Deursen, J. M. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211048 · Cited by 342 · see citing works
RETRACTED: DNA Content as a Prognostic Marker in Patients with Oral Leukoplakia
Sudbø, J., Kildal, W., Risberg, B. Å., Koppang, H. S., Danielsen, H. E., & Reith, A. (2001) · New England Journal of Medicine · doi:10.1056/nejm200104263441702 · Cited by 284 · see citing works
RetractedMolecular Pathogenesis of Osteosarcoma
Kansara, M., & Thomas, D. M. (2007) · DNA and Cell Biology · doi:10.1089/dna.2006.0505 · Cited by 273 · see citing works
Past and future of the mitotic spindle as an oncology target
Wood, K. (2001) · Current Opinion in Pharmacology · doi:10.1016/s1471-4892(01)00064-9 · Cited by 248 · see citing works
G1 and G2 cell-cycle arrest following microtubule depolymerization in human breast cancer cells
Blajeski, A. L., Phan, V., Kottke, T. J., & Kaufmann, S. H. (2002) · Journal of Clinical Investigation · doi:10.1172/jci13275 · Cited by 232 · see citing works
BUB1 and BUBR1: multifaceted kinases of the cell cycle
Bolaños-García, V. M., & Blundell, T. L. (2010) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2010.08.004 · Cited by 221 · see citing works
The Mouse Mps1p-like Kinase Regulates Centrosome Duplication
Fisk, H. A., & Winey, M. (2001) · Cell · doi:10.1016/s0092-8674(01)00411-1 · Cited by 223 · see citing works
DNA polymerase zeta (pol ζ) in higher eukaryotes
Gan, G. N., Wittschieben, J. P., Wittschieben, B. Ø., & Wood, R. D. (2007) · Cell Research · doi:10.1038/cr.2007.117 · Cited by 202 · see citing works
Epigenetic inactivation of CHFR in human tumors
Toyota, M., Sasaki, Y., Satoh, A., Ogi, K., Kikuchi, T., Suzuki, H., Mita, H., Tanaka, N., Itoh, F., Issa, J. J., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1337066100 · Cited by 199 · see citing works
Targeting the Mitotic Checkpoint for Cancer Therapy with NMS-P715, an Inhibitor of MPS1 Kinase
Colombo, R., Caldarelli, M., Mennecozzi, M., Giorgini, M. L., Sola, F., Cappella, P., Perrera, C., Depaolini, S. R., Rusconi, L., Cucchi, U., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-2101 · Cited by 198 · see citing works
Mitotic checkpoints: from yeast to cancer
Wassmann, K., & Benezra, R. (2001) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00161-1 · Cited by 195 · see citing works
FUNCTIONS AND MECHANISMS OF ACTION OF THE ADENOVIRUS E3 PROTEINS
Lichtenstein, D. L., Tóth, K., Doronin, K., Tollefson, A. E., & Wold, W. S. M. (2004) · International Reviews of Immunology · doi:10.1080/08830180490265556 · Cited by 192 · see citing works
Bub1 overexpression induces aneuploidy and tumor formation through Aurora B kinase hyperactivation
Ricke, R. M., Jeganathan, K. B., & van Deursen, J. M. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201012035 · Cited by 190 · see citing works
Fujisawa, H., Reis, R. M., Nakamura, M., Colella, S., Yonekawa, Y., Kleihues, P., & Ohgaki, H. (2000) · Laboratory Investigation · doi:10.1038/labinvest.3780009 · Cited by 180 · see citing works
Shichiri, M., Yoshinaga, K., Hisatomi, H., Sugihara, K., & Hirata, Y. (2002) · PubMed · Cited by 177 · see citing works
Aneuploid colon cancer cells have a robust spindle checkpoint
Tighe, A., Johnson, V., Albertella, M. R., & Taylor, S. S. (2001) · EMBO Reports · doi:10.1093/embo-reports/kve127 · Cited by 175 · see citing works
García‐Castillo, H., Vásquez-Velásquez, A. I., Rivera, H., & Barros‐Núñez, P. (2008) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32315 · Cited by 170 · see citing works
A Bacterial Effector Targets Mad2L2, an APC Inhibitor, to Modulate Host Cell Cycling
Iwai, H., Kim, M., Yoshikawa, Y., Ashida, H., Ogawa, M., Fujita, Y., Muller, D., Kirikae, T., Jackson, P. K., Kotani, S., et al. (2007) · Cell · doi:10.1016/j.cell.2007.06.043 · Cited by 169 · see citing works
Epigenetic inactivation of CHFR and sensitivity to microtubule inhibitors in gastric cancer.
Satoh, A., Toyota, M., Itoh, F., Sasaki, Y., Suzuki, H., Ogi, K., Kikuchi, T., Mita, H., Yamashita, T., Kojima, T., et al. (2003) · PubMed · Cited by 163 · see citing works
The spindle checkpoint: two transitions, two pathways
Gardner, R. D., & Burke, D. J. (2000) · Trends in Cell Biology · doi:10.1016/s0962-8924(00)01727-x · Cited by 153 · see citing works
SHLD2/FAM35A co‐operates with REV7 to coordinate DNA double‐strand break repair pathway choice
Findlay, S., Heath, J., Luo, V. M., Malina, A., Morin, T., Coulombe, Y., Djerir, B., Li, Z., Samiei, A., Simo‐Cheyou, E. R., et al. (2018) · The EMBO Journal · doi:10.15252/embj.2018100158 · Cited by 148 · see citing works
MAD2B is an inhibitor of the anaphase-promoting complexPreprint
Chen, J., & Fang, G. (2001) · Genes & Development · doi:10.1101/gad.898701 · Cited by 144 · see citing works
Inhibition of Cdh1–APC by the MAD2-related protein MAD2L2: a novel mechanism for regulating Cdh1Preprint
Pfleger, C. M., Salic, A. N., Lee, E. N., & Kirschner, M. W. (2001) · Genes & Development · doi:10.1101/gad.897901 · Cited by 140 · see citing works
The multifaceted roles of the HORMA domain in cellular signaling
Rosenberg, S., & Corbett, K. D. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201509076 · Cited by 132 · see citing works
Molecular alterations associated with bladder cancer initiation and progression
Cordon‐Cardo, C. (2008) · Scandinavian Journal of Urology and Nephrology · doi:10.1080/03008880802291915 · Cited by 126 · see citing works
The role of the SV40 ST antigen in cell growth promotion and transformation
Rundell, K., & Parakati, R. (2001) · Seminars in Cancer Biology · doi:10.1006/scbi.2000.0341 · Cited by 126 · see citing works
Mutations in the mitotic check point gene, MAD1L1, in human cancers
Tsukasaki, K., Miller, C. W., Greenspun, E., Eshaghian, S., Kawabata, H., Fujimoto, T., Tomonaga, M., Sawyers, C. L., SAID, J. W., & Koeffler, H. P. (2001) · Oncogene · doi:10.1038/sj.onc.1204421 · Cited by 122 · see citing works
Multiple Roles of Vertebrate REV Genes in DNA Repair and Recombination
Okada, T., Sonoda, E., Yoshimura, M., Kawano, Y., Saya, H., Kohzaki, M., & Takeda, S. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.14.6103-6111.2005 · Cited by 112 · see citing works
Novel actions of the antitumor drugs vinflunine and vinorelbine on microtubules.
Ngan, V. K., Bellman, K., Panda, D., Hill, B. T., Jordan, M. A., & Wilson, L. (2000) · PubMed · Cited by 112 · see citing works
Corn, P. G. (2003) · Carcinogenesis · doi:10.1093/carcin/24.1.47 · Cited by 106 · see citing works
CEP55 is a determinant of cell fate during perturbed mitosis in breast cancer
Kalimutho, M., Sinha, D., Jeffery, J., Nones, K., Srihari, S., Fernando, W., Duijf, P. H. G., Vennin, C., Raninga, P. V., Nanayakkara, D. M., et al. (2018) · EMBO Molecular Medicine · doi:10.15252/emmm.201708566 · Cited by 99 · see citing works
Constitutional aneuploidy and cancer predisposition
Ganmore, I., Smooha, G., & Izraeli, S. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp084 · Cited by 98 · see citing works
Imai, Y., Shiratori, Y., Kato, N., Inoue, T., & Omata, M. (1999) · Japanese Journal of Cancer Research · doi:10.1111/j.1349-7006.1999.tb00824.x · Cited by 98 · see citing works
Genetic instability: tipping the balance
Janssen, A., & Medema, R. H. (2012) · Oncogene · doi:10.1038/onc.2012.576 · Cited by 97 · see citing works
Matsuura, S., Ito, E., Tauchi, H., Komatsu, K., Ikeuchi, T., & Kajii, T. (2000) · The American Journal of Human Genetics · doi:10.1086/303022 · Cited by 95 · see citing works
Understanding familial and non-familial renal cell cancer
Bodmer, D. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.20.2489 · Cited by 92 · see citing works
Ruszkiewicz, A. R., Bennett, G., Moore, J., Manavis, J., Rudzki, B., Shen, L. Y. C., & Suthers, G. (2002) · Pathology · doi:10.1080/0031302021000035965-2 · Cited by 92 · see citing works
Cheung, H. W., Chun, A. C. S., Wang, Q., Deng, W., Hu, L., Guan, X., Nicholls, J. M., Ling, M., Wong, Y. C., Tsao, S. W., et al. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3602 · Cited by 91 · see citing works
Recent advances in cancer research: mouse models of tumorigenesis
Herzig, M., & Christofori, G. (2002) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/s0304-419x(02)00039-2 · Cited by 89 · see citing works
Koga, T., Hashimoto, S., Sugio, K., Yoshino, I., Nakagawa, K., Yonemitsu, Y., Sugimachi, K., & Sueishi, K. (2001) · International Journal of Cancer · doi:10.1002/1097-0215(20010720)95:4 · Cited by 34 · see citing works
Complexity in the spindle checkpoint
Burke, D. J. (2000) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(99)00040-4 · Cited by 88 · see citing works
Procopio, A. D., Strizzi, L., Vianale, G., Betta, P., Puntoni, R., Fontana, V., Tassi, G., Gareri, F., & Mutti, L. (2000) · Genes Chromosomes and Cancer · doi:10.1002/1098-2264(2000)9999:9999 · Cited by 52 · see citing works
Nelson, K. K., Schlöndorff, J. S., & Blobel, C. (1999) · PubMed Central · Cited by 83 · see citing works
Expression of the mitotic checkpoint gene MAD2L2 has prognostic significance in colon cancer
Rimkus, C., Friederichs, J., Rosenberg, R., Holzmann, B., Siewert, J., & Janssen, K. (2006) · International Journal of Cancer · doi:10.1002/ijc.22155 · Cited by 77 · see citing works
Weterman, M. A. J., van Groningen, J. J. M., Tertoolen, L. G. J., & van Kessel, A. G. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.241304198 · Cited by 76 · see citing works
Preventing aneuploidy: The contribution of mitotic checkpoint proteins
Suijkerbuijk, S. J. E., & Kops, G. J. P. L. (2008) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2008.04.001 · Cited by 74 · see citing works
Overexpression of B-type cyclins alters chromosomal segregation
Sarafan‐Vasseur, N., Lamy, A., Bourguignon, J., Pessot, F. L., Hieter, P., Sesboüé, R., Bastard, C., Frébourg, T., & Flaman, J. (2002) · Oncogene · doi:10.1038/sj.onc.1205257 · Cited by 74 · see citing works
On the statistical assessment of classifiers using DNA microarray data
Ancona, N., Maglietta, R., Piepoli, A., D’Addabbo, A., Cotugno, R., Savino, M., Liuni, S., Carella, M., Pesole, G., & Perri, F. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-387 · Cited by 73 · see citing works
Frequent impairment of the spindle assembly checkpoint in hepatocellular carcinoma
Saeki, A., Tamura, S., Ito, N., Kiso, S., Matsuda, Y., Yabuuchi, I., Kawata, S., & Matsuzawa, Y. (2002) · Cancer · doi:10.1002/cncr.10448 · Cited by 73 · see citing works
Cancer Karyotypes: Survival of the Fittest
Nicholson, J. M., & Cimini, D. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00148 · Cited by 70 · see citing works
Sudbø, J., & Reith, A. (2005) · International Journal of Cancer · doi:10.1002/ijc.20896 · Cited by 68 · see citing works
RetractedCAMP (C13orf8, ZNF828) is a novel regulator of kinetochore–microtubule attachment
Itoh, G., Kanno, S., Uchida, K. S. K., Chiba, S., Sugino, S., Watanabe, K., Mizuno, K., Yasui, A., Hirota, T., & Tanaka, K. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.276 · Cited by 64 · see citing works
Association of abnormal morphology and altered gene expression in human preimplantation embryos
Wells, D., García-Bermúdez, M., Steuerwald, N., Malter, H. E., Thornhill, A. R., & Cohen, J. (2005) · Fertility and Sterility · doi:10.1016/j.fertnstert.2005.01.143 · Cited by 67 · see citing works
Konttinen, Y. T., Li, T.-F., Mandelin, J., Ainola, M., Lassus, J., Virtanen, I., Santavirta, S. S., Tammi, M., & Tammi, R. (2001) · The Journal of Pathology · doi:10.1002/1096-9896(200107)194:3 · Cited by 20 · see citing works
Infrequent Mutation of the hBUB1 and hBUBR1 Genes in Human Lung Cancer
Sato, M., Sekido, Y., Horio, Y., Takahashi, M., Saito, H., Minna, J. D., Shimokata, K., & Hasegawa, Y. (2000) · Japanese Journal of Cancer Research · doi:10.1111/j.1349-7006.2000.tb00974.x · Cited by 64 · see citing works
Safeguarding Entry into Mitosis: the Antephase Checkpoint
Chin, C. F., & Yeong, F. M. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00687-09 · Cited by 63 · see citing works
Identification of Drivers of Aneuploidy in Breast Tumors
Pfister, K. E., Pipka, J. L., Chiang, C., Liu, Y., Clark, R. A., Keller, R. E., Skoglund, P., Guertin, M. J., Hall, I. M., & Stukenberg, P. T. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.102 · Cited by 65 · see citing works
Tunquist, B. J., Eyers, P. A., Chen, L. G., Lewellyn, A. L., & Maller, J. L. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200306153 · Cited by 63 · see citing works
hBUB1 defects in leukemia and lymphoma cells
Ru, H. Y., Chen, R., Lu, W. C., & Chen, J. H. (2002) · Oncogene · doi:10.1038/sj.onc.1205585 · Cited by 62 · see citing works
Targeting the Translesion Synthesis Pathway for the Development of Anti-Cancer Chemotherapeutics
Korzhnev, D. M., & Hadden, M. K. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b00596 · Cited by 58 · see citing works
de Krijger, I., Boersma, V., & Jacobs, J. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2021.04.002 · Cited by 40 · see citing works
Centrosomes and checkpoints: the MPS1 family of kinases
Winey, M., & Huneycutt, B. J. (2002) · Oncogene · doi:10.1038/sj.onc.1205712 · Cited by 58 · see citing works
The Mad1–Mad2 balancing act – a damaged spindle checkpoint in chromosome instability and cancer
Schuyler, S. C., Wu, Y.-F. O., & Kuan, V. J.-W. (2012) · Journal of Cell Science · doi:10.1242/jcs.107037 · Cited by 58 · see citing works
Hong, C.-F., Chou, Y., Lin, Y.-S., & Wu, C. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.005017 · Cited by 58 · see citing works
Targeting Mitosis for Anti-Cancer Therapy
Sudakin, V., & Yen, T. J. (2007) · BioDrugs · doi:10.2165/00063030-200721040-00003 · Cited by 57 · see citing works
Molecular mechanisms of human carcinogenesis
Coleman, W. B., & Tsongalis, G. J. (2006) · Birkhäuser Basel eBooks · doi:10.1007/3-7643-7378-4_14 · Cited by 57 · see citing works
Mitotic Checkpoint Protein hsMAD2 as a Marker Predicting Liver Metastasis of Human Gastric Cancers
Tanaka, K., Nishioka, J., Kato, K., Nakamura, A., 毛利智美, Miki, C., Kusunoki, M., & Nobori, T. (2001) · Japanese Journal of Cancer Research · doi:10.1111/j.1349-7006.2001.tb01186.x · Cited by 56 · see citing works
Chan, S., Hung, F. S. ‐., Chan, D. S. ‐., & Shaw, P. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02091.x · Cited by 56 · see citing works
Summers, M. K., Bothos, J. G., & Halazonetis, T. D. (2005) · Oncogene · doi:10.1038/sj.onc.1208428 · Cited by 55 · see citing works
Novel Management of Oral Cancer: A Paradigm of Predictive Oncology
Sudbø, J. (2004) · Clinical Medicine & Research · doi:10.3121/cmr.2.4.233 · Cited by 55 · see citing works
RetractedBubR1 kinase: protection against aneuploidy and premature aging
Kapanidou, M., Lee, S., & Bolaños-García, V. M. (2015) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2015.04.003 · Cited by 53 · see citing works
Beheshti, B., Park, P. C., Sweet, J., Trachtenberg, J., Jewett, M. A. S., & Squire, J. A. (2001) · Neoplasia · doi:10.1038/sj.neo.7900125 · Cited by 53 · see citing works
Kallio, M. J., Eriksson, J., & Gorbsky, G. J. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9818 · Cited by 53 · see citing works
The REV7 Subunit of DNA Polymerase ζ Is Essential for Primordial Germ Cell Maintenance in the Mouse
Watanabe, N., Mii, S., Asai, N., Asai, M., Niimi, K., Ushida, K., Kato, T., Enomoto, A., Ishii, H., Takahashi, M., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.421966 · Cited by 52 · see citing works
Whole chromosome instability resulting from the synergistic effects of pRB and p53 inactivation
Manning, A. L., Benes, C. H., & Dyson, N. J. (2013) · Oncogene · doi:10.1038/onc.2013.201 · Cited by 50 · see citing works
Pinto, M., Vieira, J., Ribeiro, F. R., Soares, M. J., Henrique, R., Oliveira, J., Jerónimo, C., & Teixeira, M. R. (2008) · PubMed Central · doi:10.3233/clo-2008-0439 · Cited by 49 · see citing works
Southern, S. A., & Herrington, C. S. (2000) · International Journal of Gynecological Cancer · doi:10.1046/j.1525-1438.2000.010004263.x · Cited by 49 · see citing works
Cep55 overexpression promotes genomic instability and tumorigenesis in mice
Sinha, D., Nag, P., Nanayakkara, D. M., Duijf, P. H. G., Burgess, A., Raninga, P. V., Smits, V. A. J., Bain, A. L., Subramanian, G. N., Wall, M., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-01304-6 · Cited by 48 · see citing works
Inactivating mutations targeting the chfr mitotic checkpoint gene in human lung cancer.
Mariatos, G., Bothos, J. G., Zacharatos, P., Summers, M. K., Scolnick, D. M., Kittas, C. N., Halazonetis, T. D., & Gorgoulis, V. G. (2003) · PubMed · Cited by 48 · see citing works
DNA double-strand break repair: a tale of pathway choices
Li, J., & Xu, X. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw045 · Cited by 46 · see citing works
Role of genomic instability in human carcinogenesis
Moon, J. J., Lu, A., & Moon, C. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219826031 · Cited by 46 · see citing works
Viganó, C., von Schubert, C., Ahrné, E., Schmidt, A., Lorber, T., Bubendorf, L., de Vetter, J. R. F., Zaman, G. J. R., Štorchová, Z., & Nigg, E. A. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-10-0577 · Cited by 45 · see citing works
Which putatively pre‐malignant oral lesions become oral cancers?
Sudbø, J., & Reith, A. (2003) · Journal of Oral Pathology and Medicine · doi:10.1034/j.1600-0714.2003.00054.x · Cited by 45 · see citing works
Olesen, S. H. (2001) · Carcinogenesis · doi:10.1093/carcin/22.5.813 · Cited by 45 · see citing works
Doak, S. H., Jenkins, G. J. S., Parry, E. M., Griffiths, A. P., BAXTER, J. N., & Parry, J. M. (2004) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2003.12.009 · Cited by 44 · see citing works
Characterization of Regions in hsMAD1 Needed for Binding hsMAD2
Iwanaga, Y., Kasai, T., Kibler, K. V., & Jeang, K.-T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m110666200 · Cited by 43 · see citing works
Requirement of Skp1-Bub1 Interaction for Kinetochore-Mediated Activation of the Spindle Checkpoint
Kitagawa, K., Abdulle, R., Bansal, P. K., Cagney, G., Fields, S., & Hieter, P. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00145-x · Cited by 43 · see citing works
- Authors
- Cahill, D. P., da Costa, L. T., Carson-Walter, E. B., Kinzler, K. W., Vogelstein, B., & Lengauer, C.
- Affiliations
- Johns Hopkins University (US)
- Howard Hughes Medical Institute (US)
- Venue
- Genomics
- Publisher
- Elsevier BV
- Published
- 1999-06
- Volume
- 58
- Issue
- 2
- Pages
- 181-187
- ISSN
- 0888-7543 (ISSN-L)
- OpenAlex
- W1970916591
- Cited by
- 212
- References
- 36
- Citations by year
- 2025: 2 · 2024: 2 · 2023: 7 · 2021: 4 · 2020: 3 · 2019: 4 · 2018: 5 · 2017: 4 · 2016: 5 · 2015: 11 · 2014: 1 · 2013: 6 · 2012: 6
- FWCI
- 7.21
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Genomics (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (CA62924, CA43460)
- National Cancer Institute (CA43460, P50CA062924, CA 62924)
- National Institute of General Medical Sciences (T32GM007184, GM07184)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- MAD2L2, mitotic spindle checkpoint, aneuploidy, colorectal cancer, chromosomal localization, gene structure, BUB1, Bub3, TTK, CDC20, MAD1L1, Mad2
- MeSH terms
- Amino Acid Sequence, Colonic Neoplasms, DNA Mutational Analysis, Exons, Humans, Introns, Spindle Apparatus, Molecular Sequence Data, Polymorphism, Genetic, Proteins, Tumor Cells, Cultured, Databases, Factual, Sequence Homology, Amino Acid, DNA Primers, Physical Chromosome Mapping, Mad2 Proteins
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