Cell cycle: regulatory mechanisms and biochemical markers

Authors

  • Silvia H. Rabenhorst Universidade Estadual Paulista (UNESP), Botucatu (SP), Brasil.
  • Roberto C. Burini Departamento de Clínica Médica, Faculdade de Medicina. Universidade Estadual Paulista (UNESP), Botucatu (SP), Brasil.
  • Fernando C. L. Schmitt Departamento de Patologia, Faculdade de Medicina. Universidade Estadual Paulista (UNESP), Botucatu (SP), Brasil.

DOI:

https://doi.org/10.32635/2176-9745.RBC.1994v40n3.2983

Keywords:

Cellular Cycle, Proliferative Cell, Cell-Cycle Markers, Proto-Oncogenes

Abstract

The regulatory mechanisms of the cellular cycle and its relationship with the growth factors, oncogenes end anti-oncogenes are one of the major advanced fields in the cancerbiology studies. The Identification of proteins and cofactors regulating the transitions between G1/S and G1/M as well the transcription of the genetic material have allowed the detection of cyclíng cells even before the appearance of the mitotic signs. The development of techniques using monoclonal antibodies against those proteins have made possible studies on proliferative cells of different tomours, mainly based on fact that proteins such as alpha polymerase and cyclin/PCNA are expressed only by proliferating cells. Thus the detection and counting of these cells would allow the evaluation of either the tumor-growth rate or its therapeutic efficiency and consequentiy the prognostic of the disease. The present paper reviewed the current knowledgement of the cell-cycle control mechanisms and the available methodology for the proliferative-cell detection emphasizing the biochemical markers, its practicability and reliability.

Downloads

Download data is not yet available.

References

ADDISON, C., JENKINS, J. R., STRIRZBECKER, N. W. The p53 nuclea localization signal in structurally unked to p34cdc2 kinase mothy. Oncogenes 5:423-426, 1990

BASNAKIAN, A., BENFALVI, G., SARKAR, N. Contribution of DNA polimerase delta to DNA replicatlon in permeable CHO cells synchronized in S phase. Nuclelc Acld Res. 17:4757-4767, 1989. DOI: https://doi.org/10.1093/nar/17.12.4757

BLOW, J. DNA replicatlon, Many strands converge. Nature 326:441-442, 1987.

BRAVO, R. FRANK, R., BLUNDELL, P.A., et al. Cyclin/PCNA is the auxiliary protein of DNA polymerase delta. Nature 326:515-517, 1987. DOI: https://doi.org/10.1038/326515a0

BRAVO, R. & CELIS, J.E. Asearch for differencial polypeptide synthesis throught of cell cycle of HeLa cells. J. Cell Blology 84:795-802, 1980. DOI: https://doi.org/10.1083/jcb.84.3.795

BROWN, O.C., GATTER; K.C. Monoclonal antibody ki-67: its use in histopathology. HIatopathology 17:489-503, 1990. DOI: https://doi.org/10.1111/j.1365-2559.1990.tb00788.x

BYNES, J.J., DOWONEY, K.M., BLACK, V.L., et al. Biochemistry 23:12316, 1984. Aput Blow, J. DNA replicatlon Many strands converge. Nature 326:441-42, 1987. DOI: https://doi.org/10.1038/326441a0

DIRICK, L., NASMITH, K. Positive feedback in the activition of G1 cyclins in yeast. Nature 351:754-757, 1991. DOI: https://doi.org/10.1038/351754a0

DRAETTA, G., LUCA, F., WESTENDORF, J., et al. D. cdc2 protein kinase is complexed with both cyclin A and B: Evidence for proteolitic inactivation of MPF. Cell 56:629-839, 1989. DOI: https://doi.org/10.1016/0092-8674(89)90687-9

DREATTA, G., BEACH, O. Activation of cdc2 protein kinase during mitosis in human cell: cell cycle-dependent phosphorylation and subunit rearrangement. Cell 54:17-26, 1989. DOI: https://doi.org/10.1016/0092-8674(88)90175-4

DUNPHY, W.G., BRIZUELA, L., BEACH, D., et al. The xenopus cdc2 protein is a component of MPF, a cytoplasmic regulator of mitosis. Cell 54:423-431, 1988. DOI: https://doi.org/10.1016/0092-8674(88)90205-X

FELIX, A.M., LEBBÉ, J.C., DORÉE, M. et al. Triggering of cyclin degradatlon in interphase extracts of amphibian eggs by cdc2 kinase. Nature 346:379-382, 1990. DOI: https://doi.org/10.1038/346379a0

FIDOVICH-KED, J., HANSON, L.J., KEYOMARSI, K., et al. Through the cell cycle: an overview. Am. Rev. Reep. Dis. 142:53-56, 1990. DOI: https://doi.org/10.1164/ajrccm/142.6_Pt_2.S3

GARCIA, R.L., COLTRERA, M.D., GOWN, A.M., Analysis of proliferative grade using anti-PCNA/ciclin monoclonal anti-bodies in fixed, embedded tissues. Comparison with cytometric analysis. Am. J. Pathol. 134:733-739, 1989.

GERDES, J., LI, L., SCHLVELTER, C., DUCHROW, M., et al. Immunobiochemical and molecular biologic characterization of the cell proliferation associated nuclear antigen that is defined by monoclonal antibody ki-67. Am. J. Pathol. 138: 867-873, 1991.

HARWELL, L.H. Saccharomyces cerevisiae cell cycle. Bacterlol Rev. 38:164-168, 1974. DOI: https://doi.org/10.1128/br.38.2.164-198.1974

HARTWELL, L.H., WEINERT, T. Checkpoints: Controls that ensure the order of cell cycle events. Science 246:629-634, 1989. DOI: https://doi.org/10.1126/science.2683079

HUBERMANN, J.A. Cell cycle control of initiation of eukary-otic DNA replicatlon. Chromoaaoma 100:419-423, 1992. DOI: https://doi.org/10.1007/BF00364551

HUNT, T. Cell cycle gets more cyclins. Nature 350:462-463, 1991. DOI: https://doi.org/10.1038/350462a0

KAMEL, O.W., LeBRUM, D.P., DAVIS, R.G., et al. Grown fraction estimulation of malignant lymphomas in formalen-flxed palraffln-embedded tissue using antI-PCNA/Cyclin 19A2: Correlation with ki-67. Am. J. Pathol. 138:1471-1477, 1992.

KENNY, M.L., LEE, S.H., HURWITZ, J. Multiple functions of human single-strand-DNA binding protein in Simian virus 40.

LASKEY, R.A., FAIRMAN, M.P. BLOW, J.J. S phase of cell cycle. Science 246:609-613, 1989. DOI: https://doi.org/10.1126/science.2683076

LEE, S.H., HURWITZ, L. Mechanism of elongation of primed DNA by DNA polymerase delta, proliferating cell nuclear antigen and activator. 1. Proc. Natl. Acad. Scl. USA 87: 5672-5676, 1990. DOI: https://doi.org/10.1073/pnas.87.15.5672

LEE, M.Y.: ALEJANDRO, R.; TOOMEY, N.L. - Immunochemical studies of DNA polymerase deita: relation with DNA polymerase alpha. Arch. Blochem. Blophya 272:1-9, 1989. DOI: https://doi.org/10.1016/0003-9861(89)90187-2

LEWIN, B.- Perpetuation of DNA. In: Genes II. 2aed. Toronto, John Wiley & Sons, 1985. p. 533.

LIU, Y.C.: MARRACCINO, R.L.; KENG, P.C.; et al. - Requirement for proliferating cell nuclear antigen expression during stages of the Chinese hamster ovary cell cycle. Blochemistry, 28:2967-2974, 1985. DOI: https://doi.org/10.1021/bi00433a034

MASUI, Y.; MARKET, C. - Cytoplasmic control nuclear behavior during meiotic maturation of frog oocytes. J. Exp. Zool. 177:129-146, 1971. DOI: https://doi.org/10.1002/jez.1401770202

MIYACHI, K.; FRITZLER, M.J.; TAN, E.M. - Autoantibody to a nuclear antigen in proliferating cells. J. Immunol, 121: 2228-2234. DOI: https://doi.org/10.4049/jimmunol.121.6.2228

MORENO, S.; NURSE, P.L.; RUSSEL, P. - Regulation of mitosis by cyclic acumulation of p80cdc2 mitotic inducer in fission yeast. Nature 344:549-552, 1990. DOI: https://doi.org/10.1038/344549a0

MOTOKURA, T. BLOOMM, T.; KIM, H.G.; et al. - A novel cyclin encoded by a abil-linked candidate oncogene. Nature, 350:512-515, 1991. DOI: https://doi.org/10.1038/350512a0

MURRAY, A.W.; KIRSCHNER, M.W. - Dominoes and clocks: The Union of two views of the cell cycle. Science 246: 614-621, 1989. DOI: https://doi.org/10.1126/science.2683077

MURRAY, A.W.; KIRSCHNER, M.W. - What controla the cell cycle. Sclentiflc Am. 264:34-41, 1991. DOI: https://doi.org/10.1038/scientificamerican0391-56

NORTH, G. - Starting and atopping. Nature 351:604-605, 1991. DOI: https://doi.org/10.1038/351604a0

NURSE, P. Universal control mechanism regulating on set of M-phase. Nature 344:503-508, 1990 DOI: https://doi.org/10.1038/344503a0

PARDEC, A.B. G1 events and regulation of cell proliferation. Science 244:603-608, 1989. DOI: https://doi.org/10.1126/science.2683075

PINES, J.; HUNTER, T. - Human cyclins Aand BI are differentially located in cell undergo cell cycle-dependent nuclear transpot. J. Cell Blol., 115:1-17, 1991. DOI: https://doi.org/10.1083/jcb.115.1.1

PRELICH, G.; KOSTURA, M.; MARSHAK, D.R.; et al. – The cell-cycle regulated proliferating cell nuclear antigen Is required for SV40 DNA replicatlon in vitro. Nature 326: 471-475, 1987. DOI: https://doi.org/10.1038/326471a0

PRELICH, G.; TAN, C.K.; KOSTURA, M.; et al. – Functional identity of proliferating cell nuclear antigen and a DNA polymerase delta auxiliary protein. Nature 326:517-520, 1987. DOI: https://doi.org/10.1038/326517a0

SINGER, M.; BERG, P. - DNA replication. In: Genes & Genomes. Mlll Valley, University Science Booka, 1991. p. 73-128.

SMITH, L.; CKER, R. - The interaction of steroids with Rana pipiens oocytes In the induction of maturation. Dev. Blol. 25: 233-247, 1971. DOI: https://doi.org/10.1016/0012-1606(71)90029-7

SUGAWARA, I.; UCHINO, K.; MOROSHITA, Y.; et al. - Intracellular localization of a subunit of human DNA polymerase alpha affecting primase activity recognised by monoclonal antibody (HDR-859-E4) and its appiication to distinction between proliferative and non-proliferative lesion. Br. J. Cancer 60:176-181, 1989. DOI: https://doi.org/10.1038/bjc.1989.246

SUZUKA, I.; DAIDOGI, H.; MATSUOKA, M.; et al. Gene for proliferating-ceçll nuclear antigen (DNA plymerase delta auxiliary protein) is present In both mammalian and higher plant genomes. Proc. Natl. Acad. Scl. USA 86:3189-93, 1989. DOI: https://doi.org/10.1073/pnas.86.9.3189

TSURIMOTO, T.; STILLMAN, B. - Multiple replication factors augment DNA synthesis by the two eukaryotic DNA polymerase, alpha and delta. EMBO J 8:3883-3889, 1989. DOI: https://doi.org/10.1002/j.1460-2075.1989.tb08567.x

TSURIMOTO, T; MELANDY, T.; STILLMAN, B. – Sequential initiation of lagging and leading strand synthesis by two different polymerase complexes at SV40 DNA replication origin. Nature 346:534-539, 1990. DOI: https://doi.org/10.1038/346534a0

Published

2023-06-05

How to Cite

1.
Rabenhorst SH, Burini RC, Schmitt FCL. Cell cycle: regulatory mechanisms and biochemical markers. Rev. Bras. Cancerol. [Internet]. 2023 Jun. 5 [cited 2024 May 17];40(3):141-7. Available from: https://rbc.inca.gov.br/index.php/revista/article/view/2983

Issue

Section

ORIGINAL ARTICLE