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Year 2020, Volume: 24 Issue: 1, 265 - 271, 01.02.2020
https://doi.org/10.16984/saufenbilder.559820

Abstract

References

  • M. Li, and P. Zhang, “Spindle Assembly Checkpoint, Aneuploidy, and Tumorigenesis” Cell cycle (Georgetown, Tex), vol. 8, no. 21, pp. 3440, 2009.
  • A. Musacchio, “The Molecular Biology of Spindle Assembly Checkpoint Signaling Dynamics.” Current Biology, vol. 25, no. 20, pp R1002-1018, 2015.
  • C. Dominguez-Brauer, KL. Thu, JM. Mason, H. Blaser, MR. Bray and TW Mak, “Targeting Mitosis in Cancer: Emerging Strategies” Molecular Cell, vol. 60 no. 4 pp. 524-536, 2015.
  • MA. Jordan and K. Kamath, “How do microtubule-targeted drugs work? An overview.” Current Cancer Drug Targets, vol. 7, no. 8, pp. 730-742, 2007.
  • HC. Huang, J. Shi, JD. Orth and TJ. Mitchison, “Cell death when the SAC is out of commission.” Cell Cycle, vol. 9, no. 11, pp. 2049-2050, 2010.
  • KM. Minhas, B. Singh, WW. Jiang, D. Sidransky and JA. Califano, “Spindle assembly checkpoint defects and chromosomal instability in head and neck squamous cell carcinoma.” International Journal of Cancer, vol.107, no. 1, pp. 46-52, 2003.
  • V. Rossio, E. Galati and S. Piatti, “Adapt or die: how eukaryotic cells respond to prolonged activation of the spindle assembly checkpoint.” Biochemical Society Transactions, vol. 38, no. 6, pp. 1645-1649, 2010.
  • CL. Rieder and H. Maiato, “Stuck in division or passing through: what happens when cells cannot satisfy the spindle assembly checkpoint.” Developmental Cell, vol. 7, no. 5, pp. 637-651, 2004.
  • CC. Stobbe, SJ. Park and D. Chapman, “The radiation hypersensitivity of cells at mitosis.” International Journal of Radiation Biology, vol. 78, no. 12, pp. 1149-1157, 2002.
  • H. Sies, C. Berndt and DP. Jones, “Oxidative Stress.” Annual Review of Biochemistry, vol. 86, pp. 715-748, 2017.
  • JE. Klaunig, LM. Kamendulis and BA. Hocevar, “Oxidative stress and oxidative damage in carcinogenesis.” Toxicologic Pathology, vol. 38, no. 1, pp. 96-109, 2010.
  • G-Y. Liou and P. Storz, “Reactive oxygen species in cancer.” Free Radical Research, vol. 44, no. 5, pp. 479-496, 2010.
  • T. Stylianopoulos, “The solid mechanics of cancer and strategies for improved therapy.” Journal of Biomechanical Engineering, vol. 139, no. 2, pp. 10, 2017.
  • M. Delarue, F. Montel, D. Vignjevic, J. Prost, J-F. Joanny and G. Cappello, “Compressive Stress Inhibits Proliferation in Tumor Spheroids through a Volume Limitation.” Biophysical Journal, vol. 107, no. 8, pp. 1821-1828, 2014.
  • DJ. McGrail, KM. McAndrews, CP. Brandenburg, N. Ravikumar, QM. Kieu and MR. Dawson, “Osmotic Regulation Is Required for Cancer Cell Survival under Solid Stress.” Biophysical Journal, vol. 109, no. 7, pp. 1334-1337, 2017.
  • C. Voutouri and T. Stylianopoulos, “Evolution of osmotic pressure in solid tumors.” Journal of Biomechanics, vol. 47, no. 14, pp. 3441-3447, 2014.
  • F. Madeo, E. Fröhlich, M. Ligr, M. Grey, SJ. Sigrist and DH. Wolf, “Oxygen stress: a regulator of apoptosis in yeast.” The Journal of Cell Biology, vol. 145, no. 4, pp. 757-767, 1999.
  • J. Liu and Z. Wang, “Increased Oxidative Stress as a Selective Anticancer Therapy.” Oxidative Medicine and Cellular Longevity, vol. 2015, 294303, 2015.
  • D. Wu and P. Yotnda, “Production and Detection of Reactive Oxygen Species (ROS) in Cancers.” Journal of Visualized Experiments, vol. 57, pp. 3357, 2011.
  • DT. Lau and AW. Murray, “Mad2 and Mad3 cooperate to arrest budding yeast in mitosis.” Current Biology, vol. 22, no. 3, pp. 180-190, 2012.
  • JA. Flattery-O'Brien and IW. Dawes, “Hydrogen peroxide causes RAD9-dependent cell cycle arrest in G2 in Saccharomyces cerevisiae whereas menadione causes G1 arrest independent of RAD9 function.” The Journal of Biological Chemistry, vol. 273, no. 15, pp. 8564-8571, 1998.
  • RE. Shackelford, WK. Kaufmann and RS. Paules, “Oxidative stress and cell cycle checkpoint function.” Free Radical Biology & Medicine, vol. 28, no. 9, pp. 1387-1404, 2000.
  • H. Saito and F. Posas, “Response to hyperosmotic stress.” Genetics, vol. 192, no. 2, pp. 289-318, 2012.

Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast

Year 2020, Volume: 24 Issue: 1, 265 - 271, 01.02.2020
https://doi.org/10.16984/saufenbilder.559820

Abstract

Cancer
cells are defined by abnormal and unrestricted mitotic divisions, therefore
targeting mitosis is a useful strategy for cancer treatment. Two groups of
drugs that are most successfully used in the treatment of several types of
cancer, taxanes and vinca
alkaloids, exhibit their anti-tumor effects by causing a mitotic arrest.
However, not much is known about whether being arrested in mitosis affects the
sensitivity of cells to tumor-related stresses, such as oxidative and osmotic
stresses. In this study, we investigated whether mitosis affects the
sensitivity of Saccharomyces cerevisiae
cells to H2O2-induced oxidative stress and
sorbitol-induced osmotic stress. Mitotic and G1-arrests were induced by
nocodazole and alpha factor, respectively. The effects of nocodazole or alpha
factor treatments on the sensitivity of
wild type (WT) and MAD3 deletion (mad3Δ) strains to
oxidative stress and osmotic stress were evaluated by the spotting and coloni
forming unit (cfu) assays as well as detection of reactive oxygen species (ROS)
production.
Data were
analyzed using Student’s t-test and expressed as standard deviation (std), p<0.05 was considered significant. Our data indicate that mitosis
significantly increases resistance to oxidative stress, however it
does not have any significant effect on the osmotic stress resistance in yeast.

References

  • M. Li, and P. Zhang, “Spindle Assembly Checkpoint, Aneuploidy, and Tumorigenesis” Cell cycle (Georgetown, Tex), vol. 8, no. 21, pp. 3440, 2009.
  • A. Musacchio, “The Molecular Biology of Spindle Assembly Checkpoint Signaling Dynamics.” Current Biology, vol. 25, no. 20, pp R1002-1018, 2015.
  • C. Dominguez-Brauer, KL. Thu, JM. Mason, H. Blaser, MR. Bray and TW Mak, “Targeting Mitosis in Cancer: Emerging Strategies” Molecular Cell, vol. 60 no. 4 pp. 524-536, 2015.
  • MA. Jordan and K. Kamath, “How do microtubule-targeted drugs work? An overview.” Current Cancer Drug Targets, vol. 7, no. 8, pp. 730-742, 2007.
  • HC. Huang, J. Shi, JD. Orth and TJ. Mitchison, “Cell death when the SAC is out of commission.” Cell Cycle, vol. 9, no. 11, pp. 2049-2050, 2010.
  • KM. Minhas, B. Singh, WW. Jiang, D. Sidransky and JA. Califano, “Spindle assembly checkpoint defects and chromosomal instability in head and neck squamous cell carcinoma.” International Journal of Cancer, vol.107, no. 1, pp. 46-52, 2003.
  • V. Rossio, E. Galati and S. Piatti, “Adapt or die: how eukaryotic cells respond to prolonged activation of the spindle assembly checkpoint.” Biochemical Society Transactions, vol. 38, no. 6, pp. 1645-1649, 2010.
  • CL. Rieder and H. Maiato, “Stuck in division or passing through: what happens when cells cannot satisfy the spindle assembly checkpoint.” Developmental Cell, vol. 7, no. 5, pp. 637-651, 2004.
  • CC. Stobbe, SJ. Park and D. Chapman, “The radiation hypersensitivity of cells at mitosis.” International Journal of Radiation Biology, vol. 78, no. 12, pp. 1149-1157, 2002.
  • H. Sies, C. Berndt and DP. Jones, “Oxidative Stress.” Annual Review of Biochemistry, vol. 86, pp. 715-748, 2017.
  • JE. Klaunig, LM. Kamendulis and BA. Hocevar, “Oxidative stress and oxidative damage in carcinogenesis.” Toxicologic Pathology, vol. 38, no. 1, pp. 96-109, 2010.
  • G-Y. Liou and P. Storz, “Reactive oxygen species in cancer.” Free Radical Research, vol. 44, no. 5, pp. 479-496, 2010.
  • T. Stylianopoulos, “The solid mechanics of cancer and strategies for improved therapy.” Journal of Biomechanical Engineering, vol. 139, no. 2, pp. 10, 2017.
  • M. Delarue, F. Montel, D. Vignjevic, J. Prost, J-F. Joanny and G. Cappello, “Compressive Stress Inhibits Proliferation in Tumor Spheroids through a Volume Limitation.” Biophysical Journal, vol. 107, no. 8, pp. 1821-1828, 2014.
  • DJ. McGrail, KM. McAndrews, CP. Brandenburg, N. Ravikumar, QM. Kieu and MR. Dawson, “Osmotic Regulation Is Required for Cancer Cell Survival under Solid Stress.” Biophysical Journal, vol. 109, no. 7, pp. 1334-1337, 2017.
  • C. Voutouri and T. Stylianopoulos, “Evolution of osmotic pressure in solid tumors.” Journal of Biomechanics, vol. 47, no. 14, pp. 3441-3447, 2014.
  • F. Madeo, E. Fröhlich, M. Ligr, M. Grey, SJ. Sigrist and DH. Wolf, “Oxygen stress: a regulator of apoptosis in yeast.” The Journal of Cell Biology, vol. 145, no. 4, pp. 757-767, 1999.
  • J. Liu and Z. Wang, “Increased Oxidative Stress as a Selective Anticancer Therapy.” Oxidative Medicine and Cellular Longevity, vol. 2015, 294303, 2015.
  • D. Wu and P. Yotnda, “Production and Detection of Reactive Oxygen Species (ROS) in Cancers.” Journal of Visualized Experiments, vol. 57, pp. 3357, 2011.
  • DT. Lau and AW. Murray, “Mad2 and Mad3 cooperate to arrest budding yeast in mitosis.” Current Biology, vol. 22, no. 3, pp. 180-190, 2012.
  • JA. Flattery-O'Brien and IW. Dawes, “Hydrogen peroxide causes RAD9-dependent cell cycle arrest in G2 in Saccharomyces cerevisiae whereas menadione causes G1 arrest independent of RAD9 function.” The Journal of Biological Chemistry, vol. 273, no. 15, pp. 8564-8571, 1998.
  • RE. Shackelford, WK. Kaufmann and RS. Paules, “Oxidative stress and cell cycle checkpoint function.” Free Radical Biology & Medicine, vol. 28, no. 9, pp. 1387-1404, 2000.
  • H. Saito and F. Posas, “Response to hyperosmotic stress.” Genetics, vol. 192, no. 2, pp. 289-318, 2012.
There are 23 citations in total.

Details

Primary Language English
Subjects Structural Biology
Journal Section Research Articles
Authors

Pinar Buket Atalay This is me 0000-0001-7627-0291

Nur Kaluc This is me 0000-0002-7323-3150

Elif Ergin Cavusoglu This is me 0000-0002-0573-6047

Publication Date February 1, 2020
Submission Date May 2, 2019
Acceptance Date October 17, 2019
Published in Issue Year 2020 Volume: 24 Issue: 1

Cite

APA Atalay, P. B., Kaluc, N., & Cavusoglu, E. E. (2020). Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast. Sakarya University Journal of Science, 24(1), 265-271. https://doi.org/10.16984/saufenbilder.559820
AMA Atalay PB, Kaluc N, Cavusoglu EE. Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast. SAUJS. February 2020;24(1):265-271. doi:10.16984/saufenbilder.559820
Chicago Atalay, Pinar Buket, Nur Kaluc, and Elif Ergin Cavusoglu. “Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast”. Sakarya University Journal of Science 24, no. 1 (February 2020): 265-71. https://doi.org/10.16984/saufenbilder.559820.
EndNote Atalay PB, Kaluc N, Cavusoglu EE (February 1, 2020) Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast. Sakarya University Journal of Science 24 1 265–271.
IEEE P. B. Atalay, N. Kaluc, and E. E. Cavusoglu, “Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast”, SAUJS, vol. 24, no. 1, pp. 265–271, 2020, doi: 10.16984/saufenbilder.559820.
ISNAD Atalay, Pinar Buket et al. “Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast”. Sakarya University Journal of Science 24/1 (February 2020), 265-271. https://doi.org/10.16984/saufenbilder.559820.
JAMA Atalay PB, Kaluc N, Cavusoglu EE. Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast. SAUJS. 2020;24:265–271.
MLA Atalay, Pinar Buket et al. “Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast”. Sakarya University Journal of Science, vol. 24, no. 1, 2020, pp. 265-71, doi:10.16984/saufenbilder.559820.
Vancouver Atalay PB, Kaluc N, Cavusoglu EE. Effect of Mitosis on the Resistance to Oxidative and Osmotic Stresses in Yeast. SAUJS. 2020;24(1):265-71.