Circadian clock, cancer and lipid metabolism

Neuroscience Research

Volumn 57, Issue 4, 2007, Pages 483-490

  Ishida, Norio ^a,b  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^b UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

Cancer; Circadian; Lipid

Indexed keywords

CELL CYCLE; CHOLESTEROL METABOLISM; CIRCADIAN RHYTHM; ENVIRONMENTAL STRESS; GENE EXPRESSION; GENETIC ANALYSIS; HIBERNATION; LIPID METABOLISM; NONHUMAN; OBESITY; PRIORITY JOURNAL; REVIEW;

ANIMALS; CELL CYCLE; CELL CYCLE PROTEINS; CIRCADIAN RHYTHM; FEEDBACK, BIOCHEMICAL; GENE EXPRESSION REGULATION; HUMANS; LIPID METABOLISM; MODELS, BIOLOGICAL; NEOPLASMS;

EID: 33947145124     PISSN: 01680102     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neures.2006.12.012     Document Type: Review

References (54)

1. Balsalobre A., Brown S.A., Marcacci L., et al. Resetting of circadian time in peripheral tissues by glucocorticoid signaling. Science 289 (2000) 2344-2347
2. Barnes J.W., Tischkau S.A., Barnes J.A., Mitchell J.W., Burgoon P.W., Hickok J.R., and Gillette M.U. Requirement of mammalian Timeless for circadian rhythmicity. Science 302 (2003) 439-442
3. Benna C., Scannapieco P., Piccin A., Sandrelli F., Zordan M., Rosato E., Kyriacou C.P., Valle G., and Costa R. A second timeless gene in Drosophila shares greater sequence similarity with mammalian tim. Curr. Biol. 10 (2000) R512-R513
4. Borjigin J., Deng J., Wang M.M., Li X., Blackshaw S., and Snyder S.H. Circadian rhythm of patched1 transcription in the pineal regulated by adrenergic stimulation and cAMP. J. Biol. Chem. 274 49 (1999) 35012-35015
5. Buijs R.M., Van Eden C.G., Goncharuk V.D., and Kalsbeek A. The biological clock tunes the organs of the body: timing by hormones and the autonomic nervous system. J. Endocrinol. 177 (2003) 17-26
6. Chan R.C., Chan A., Jeon M., Wu T.F., Pasqualone D., Rougvie A.E., and Meyer B.J. Chromosome cohesion is regulated by a clock gene paralogue TIM-1. Nature 423 (2003) 1002-1009
7. Dark J. Annual lipid cycles in hibernators: integration of physiology and behavior. Annu. Rev. Nutr. 25 (2005) 469-497
8. Dunlap J.C. Molecular bases for circadian clocks. Cell 96 (1999) 271-290
9. Fu L., Pelicano H., Liu J., Huang P., and Lee C. The circadian gene Period2 plays an important role in tumor suppression and DNA damage response in vivo. Cell 111 1 (2002) 41-50
10. Gooley J.J., Schomer A., and Saper C.B. The dorsomedial hypothalamic nucleus is critical for the expression of food-entrainable circadian rhythms. Nat. Neurosci. 9 (2006) 300-302
11. Gorbacheva U.Y., Kondratov R.V., Zhang R., Cherukuri S., Gudkov A.V., Takahashi J.S., and Antoch M.P. Circadian sensitivity to the chemotherapeutic agent cyclophosphamide depends on the functional status of the CLOCK/BMAL1 transactivation complex. Proc. Natl. Acad. Sci. U.S.A. 102 9 (2005) 3407-3412
12. Hagiwara S.Y., Bolige A., Zhang Y., Takahashi M., Yamagishi A., and Goto K. Circadian gating of photoinduction of commitment to cell-cycle transitions in relation to photoperiodic control of cell reproduction in Euglena. Photochem. Photobiol. 76 1 (2002) 105-115
13. Hamprecht B., Nussler C., and Lynen F. Rhythmic changes of hydroxymethylglutaryl coenzyme A reductase activity in livers of fed and fasted rats. FEBS Lett. 4 (1969) 117-121
14. Hastings M.H. Circadian clocks. Curr. Biol. 7 (1997) R670-R672
15. Hirayama J., Luca C., Doi M., and Paolo S-Colsi. Common pathways in circadian and cell cycle clocks: light-dependent activation of Fos/AP-1 in zebrafish controls CRY-1a and WEE-1. PNAS 02.29 (2005) 10194-10199
16. Iitaka C., Miyazaki K., Akaike T., and Ishida N. A role for glycogen synthase kinase-3β in the mammalian circadian clock. J. Biol. Chem. 280 33 (2005) 29397-29402
17. Ishida N.A., Mutoh T., Ueyama T., Bando H., Masuibuchi S., Nakahara D., Tsujimoto G., and Okamura H. Light activates the adrenal gland: timing of gene expression and glucocorticoid release. Cell Metab. 2 (2005) 297-307
18. Ishida N., Kaneko M., and Allada R. Biological clocks. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 8819-8820
19. Ishida N., Miyazaki K., and Sakai T. Circadian rhythm biochemistry: from protein degradation to sleep and mating. BBRC 286 (2001) 1-5
20. Jurevics H., Hostettler J., Barrett C., Morell P., and Toews A.D. Diurnal and dietary-induced changes in cholesterol synthesis correlate with levels of mRNA for HMG-CoA reductase. J. Lipid Res. 41 (2000) 1048-1054
21. Kawasaki H., Komai K., Nakamura M., Yamamoto E., Ouyang Z., Nakashima T., Morisawa T., Hashiramoto A., Shiozawa K., Ishikawa H., et al. Human wee1 kinase is directly transactivated by and increased in association with c-Fos/AP-1: rheumatoid synovial cells overexpressing these genes go into aberrant mitosis. Oncogene 22 (2003) 6839-6844
22. Keziban U.-K., Mullen T.E., William K.K., and Aziz S. Coupling of human circadian and cell cycles by the Timeless protein. Mol. Cell. Biol. 25 8 (2005) 3109-3116
23. Koike N., Hida A., Numano R., Hirose M., Sakai Y., and Tei H. Identification of the mammalian homologues of the Drosophila timeless gene. FEBS Lett. 441 (1998) 427-431
24. Kobayashi H., Oishi K., Hanai S., and Ishida N. Effect of feeding onperipheral circadian rhythms and behaviour in mammals. Gene Cells 9 (2004) 857-864
25. Koyanagi S., Kuramoto Y., Nakagawa H., Aramaki H., Ohdo S., Soeda S., and Shimeno H. A molecular mechanism regulating circadian expression of vascular endothelial growth factor in tumor cells. Cancer Res. 63 (2003) 7277-7283
26. Li Z., Stuart R.O., Quao J., Pavlova A., Bush K.T., Pohl M., Sakurai H., and Nigam S.K. A role for Timeless in epithelial morphogenesis during kidney development. Proc. Natl. Acad. Sci. U.S.A. 97 (2000) 10038-10043
27. Lowrey P., and Takahashi J.S. Mammalian circadian biology: elucidating genome-wide levels of temporal organization. Annu. Rev. Genomics Hum. Genet. 5 (2004) 407-441
28. Matsuo T., Yamaguchi S., Mitsui S., Emi A., Shimoda F., and Okamura H. Control mechanism of the circadian clock for timing of cell division in vivo. Science 302 (2003) 255-259
29. Miyazaki K., Nagase T., Mesaki M., Narukawa J., Ohara O., and Ishida N. Phosphorylation of clock protein PER1 regulates its circadian degradation in normal human fibroblasts. Biochem. J. 380 (2004) 95-103
30. Nagoshi E., Saini C., Bauer C., Laroche T., Naef F., and Scibler U. Circadian gene expression in individual fibroblasts: cell-autonomous and self-sustained oscillators pass time to daughter cells. Cell 119 (2004) 693-705
31. Nakagawa H., Koyanagi S., Takiguchi T., Kuramoto Y., Soeda S., Shimeno H., Higuchi S., and Ohdo S. 24-hour oscillation of mouse methionine aminopeptidase2, a regulator of tumor progression, is regulated by clock gene proteins. Cancer Res. 64 22 (2004) 8328-8333
32. Noguchi E., Noguchi C., Du L.L., and Russell P. Swi1 prevents replication fork collapse and controls checkpoint kinase Cds1. Mol. Cell. Biol. 23 (2003) 7861-7874
33. Nyberg K., Michelson A.R.J., Putnam C.W., and Weinert T.A. Toward maintaining the genome: DNA damage and replication checkpoints. Annu. Rev. Genet. 36 (2002) 617-656
34. Ochi M., Sono S., Sei H., Oishi K., Kobayashi H., Morita Y., and Ishida N. Sex difference in circadian period of body temperature in Clock mutant mice with Jcl/ICR background. Neurosci. Lett. 347 (2003) 163-166
35. Oishi K., Miyazaki K., and Ishida N. Functional CLOCK is not involved in the entrainment of peripheral clocks to the restricted feeding: entrainable expression of mPer2 and BMAL1 mRNAs in the heart of Clock mutant mice on Jcl:ICR background. BBRC 298 (2002) 198-202
36. Oishi K., Miyazaki K., Kadota K., Kikuno R., Nagase T., Atsumi G., Ohkura N., Azama T., Messaki M., Yukimasa S., Kobayashi H., Iitaka C., Umehara T., Horikoshi M., Kudo T., Shimizu Y., Yano M., Monden M., Machida K., Matsuda J., Horie S., Todo T., and Ishida N. Genome-wide expression analysis of mouse liver reveals CLOCK-regulated circadian output genes. J. Biol. Chem. 278 42 (2003) 41519-41527
37. Oishi K., Amagai N., Shirai H., Kadota K., Ohkura N., and Ishida N. Genome-wide expression analysis reveals 100 adrenal gland-dependent circadian genes in the mouse liver. DNA Res. 12 (2005) 191-202
38. Oishi K., Kobayashi H., Hanai S., and Ishida N. CLOCK is involved in the circadian transactivation of peroxisome-proliferator-activated receptor α(PPARα) in mice. Biochem. J. 386 (2005) 575-581
39. Oishi K., Atsumi G., Sugiyama S., Kodomari I., Kasamatsu M., Machida K., and Ishida N. Disrupted fat absorption attenuates obesity induced by a high-fat diet in Clock mutant mice. FEBS Lett. 580 (2006) 127-13030
40. Oishi K., Ohkura N., Wakabayashi M., Shirai H., Atsumi G., Sato K., Matsuda J., and Ishida N. CLOCK is involved in obesity-induced disordered fiblynosis in ob/ob mice by regulating PAI-1 gene expression. J. Thromb. Haemost. 4 8 (2006) 1774-1780
41. Oishi, K., Ohkura, N., Kadota, K, Kasamatsu, M., Shibukawa, K., Machida, K., Matsuda, J., Horie, S., Ishida, N., 2006c. Clock mutation affects the circadian regulation of numbers of peripheral circulating blood cells. J. Circadian Rhythm, in press.
42. Park H., and Sternglanz R. Identification and characterization of the genes for two topoisomerase I-interacting proteins from Saccharomyces cerevisiae. Yeast 15 (1999) 35-41
43. Patel D.D., Knight B.L., Wiggins D., Humphreys S.M., and Gibbons G.F. Disturbances in the normal regulation of SREBP-sensitive genes in PPAR alpha-deficient mice. J. Lipid Res. 42 3 (2001) 328-337
44. Russell P., and Nurse P. Negative regulation of mitosis by wee1, a gene encoding a protein kinase homolog. Cell 49 (1987) 559-567
45. Sakamoto K., Nagase T., Hukui H., Horikawa K., Okada T., Tanaka H., Sato K., Miyake Y., Ohara O., Kako K., and Ishida N. Multitissue circadian expression of rat period homolog (rPer2) mRNA is governed by the mammalian circadian clock, the suprachiasmatic nucleus in the brain. J. Biol. Chem. 273 (1998) 27039-27042
46. Sakamoto S., Miyazaki K., Fukui H., Oishi K., Hayasaka N., Okada M., Kamakura M., Taniguchi T., Nagai K., and Ishida N. Molecular characterization and nuclear localization of rat timeless-like gene product. BBRC 279 (2000) 131-138
47. Sangoram A.M., Saez L., Antoch M.P., Gekakis N., Staknis D., Whiteley A., Fruechte E.M., Vitaterna M.H., Shimomura K., King D.P., Young M.W., Weitz C.J., and Takahashi J.S. Mammalian circadian autoregulatory loop: a timeless ortholog and mPer1 interact and negatively regulate CLOCK-BMAL1-induced transcription. Neuron 21 (1998) 1101-1113
48. Schibler U., and Sassone-corsi P. A web of circadian pacemakers. Cell 111 (2002) 919-922
49. Schibler U., Juergen R., and Steven A.B. Peripheral circadian oscillators in mammals: time and food. J. Biol. Rhythms 18 3 (2003) 250-260
50. Shaw P.J., Tononi G., Greenspan R.J., and Robinson D.F. Stress response genes protect against lethal effects of sleep deprivation in Drosophila. Nature 16. 417 6886 (2002) 287-291
51. Turek F.W., Joshu C., Kohsaka A., Lin E., Ivanova G., McDearmon E., Laposky A., Losee-Olson S., Easton A., Jensen D.R., Eckel R.H., Takahashi J.S., and Bass J. Obesity and metabolic syndrome in circadian Clock mutant mice. Science 308 5724 (2005) 1043-1045
52. You S., Wood P.A., Xiong Y., Kobayashi M., Du-Quiton J., and Hrushesky W.J. Daily coordination of cancer growth and circadian clock gene expression. Breast Cancer Res. Treat. 91 1 (2005) 47-60
53. Vitaterna M.H., King D.P., Chang A.M., Kornhauser J.M., Lowrey P.L., McDonald J.D., Cove W.F., Pinto L.H., Turek F.W., and Takahashi J.S. Mutagenesis and mapping of a mouse gene, Clock, essential for circadian behavior. Science 264 (1994) 719-725
54. Zhang J., Kaasik K., Blackburn M.R., and Lee C.C. Constant darkness is a circadian metabolic signal in mammals. Nature 439 7074 (2006) 340-343