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2007 | 10 | 2 |

Tytuł artykułu

Possible implications of redox-sensitive tumour cell transformation: lessons from cell culture studies

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
It is generally accepted that chronic inflammatory disease, either local or generalized, is associated with higher incidence of cancer. Since inflammation is often accompanied by oxidative stress the latter was indicated as the foundation for progressive mutations leading to tumor development (proliferation, invasion, metastasis). Even though, it is very hard to demonstrate by in vitro studies the causal relationship between oxidative stress and cell transformations. From our studies it is clear that cells are more likely to stop divisions and they commit suicide by apoptosis. During last decade, a novel view on the origin of cancer emerged. The so called cancer stem cells (CSC) were found that form the side-population of stem cells (SC) and they are believed to initiate cancer. Are the SC ancestors for CSC? Do SC transform into CSC? These and other questions remain unanswered. We hypothesize that SC might undergo transformation into CSC during prolonged oxidative stress. We claim that several changes in cell biochemistry has to occur to start the molecular modifications leading to neoplasma. These include either hypoxia-promoted apoptosis signal inducing kinase 1 (ASK-1), hypoxia inducing factor 1 alpha (HIF-la) and glycolysis, or normoxia-promoted activating protein-1 (AP-1) or hyperoxia-induced nuclear factor kappa B (NF-kB). Next, harsh microenviron- ment and heterogenous extracellular matrix (ECM) induced by oxidative stress accelerate the selection of clones of cells resistant to apoptogenic signal. HIF-la, protein crucial for transcriptional activation of protooncogene met leads to the overexpression of c-Met receptor that in turn sensitizes cells to hepatocyte growth factor/scatter factor (HGF/SF) mitogen. Finally, both impaired function of mitochondria and hypoxia elevate fibrin protein level and amplify hemostasis as disseminated in- tracapillary coagulation (DIC). In any case, it is very interesting and remains to be answered whether imbalance in prooxidant-antioxidant homeostasis has causal relationship with transformation of SC to CSC.

Wydawca

-

Rocznik

Tom

10

Numer

2

Opis fizyczny

p.123-126,ref.

Twórcy

  • Warsaw Agricultural University, Nowoursynowska 159C, 02-776 Warsaw, Poland

Bibliografia

  • Calabrese EJ, Baldwin LA (1998) Hormesis as a biological hypothesis. Environ Health Perspect 106: 357-362.
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  • Karbowski M, Lee Y-J, Gaume B, Jeong S-Y, Frank S, Nechuhstan A, Santel A, Fuller M, Smith CL, Youle RJ (2002) Spatial and temporal association of Bax with mitochondrial fission sites, Drpl, and Mfn2 during apo­ptosis. J Cell Biol 159: 931-938.
  • Mackenzie IC (2005) Retention of stem cell patterns in malignant cell lines. Cell Prolif 38: 347-355.
  • Orzechowski A, Grizard J, Jank M, Gajkowska B, Lokociejewska M, Zaron-Teperek M, Godlewski MM (2002) Dexamethasone-mediated regulation of death and differentiation of muscle cells. Is hydrogen peroxide involved in the process? Reprod Nutr Dev 42: 197-216.
  • Orzechowski A, Grzelkowska K (2000a) Reactive oxygen species (ROS) and reactive nitrogen species (RNS) alter metabolic effect of insulin in rat L6 satellite cells. Pol J Vet Sci 3: 3-12.
  • Orzechowski A, Grzelkowska K (2000b) Apoptotic effect of reactive oxygen/nitrogen species (ROS/RNS) in rat L6 satellite cells. Pol J Vet Sci 3: 193-195.
  • Orzechowski A, Jank M, Gajkowska B, Sadkowski T, God­lewski MM, Ostaszewski P (2003) Delineation of sig­nalling pathway leading to antioxidant-dependent inhi­bition of dexamethasone-mediated muscle cell death. J Muscle Res Cell Motility 24: 33-53.
  • Orzechowski A, Ostaszewski P, Jank M, Berwid SJ (2002) Bioactive substances of plant origin in food - impact on genomics. Repr Nutr Dev 42: 1-17.
  • Orzechowski A., Grzelkowska K., Zimowska V., Skierski J., Ptoszaj T., Bachanek K., Motyl T., Karlik W., Filipecki M (2000) Induction of apoptosis and NF-kB by quer­cetin in growing murine L1210 lymphocytic leukaemic cells potentiated by TNF-a. Repr Nutr Dev 40: 441-465.
  • Pająk B, Gajkowska B, Orzechowski A (2005a) Cyc- loheximide-mediated sensitization to TNF-a-induced apoptosis in human colorectal cancer cell line COLO 205; role of FLIP and metabolic inhibitors. J Physiol Pharmacol 56(Suppl 3): 101-118.
  • Pająk B, Gajkowska B, Orzechowski A (2005b) Position of STAT-la in cycloheximide-dependent apoptosis trig­gered by TNF-a in human colorectal COLO 205 cancer cell line: role of polyphenolic compounds. J. Physiol. Pharmacol. 56(Suppl. 3): 119-141.
  • Pawlikowska P, Gajkowska B, Orzechowski A (2006) Mitofusin 2 (Mfn2) - a key player in insulin-dependent myogenesis in vitro. Cell Tissue Res 327: 571-581
  • Penacchietti S, Michieli P, Galluzo M, Massone M, Gior­dano S, Comoglio PM (2003) Hypoxia promotes invas­ive growth by transcriptional activation of the met proto­oncogene. Cancer Cell 3: 347-361.
  • Rhee SG (2006) H2O2, a necessary evil for cell signaling. Science 312: 1882-1883.
  • Selak MA, Armour SM, MacKenzie ED, Boulahbel H, Watson DG, Mansfield KD, Pan Y, Simon MC, Thom­pson CB, Gottlieb E (2005) Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-la prolyl hydroxylase. Cancer Cell 7: 77-85.
  • Turpaev KT (2002) Reactive oxygen species and regulation of gene expression. Biochemistry (Mosc) 67: 281-292.
  • Zimowska W, Motyl T, Skierski J, Balasińska B, Ploszaj T, Orzechowski A, Filipecki M (1997) Apoptosis and Bcl-2 protein changes in L1210 leukaemic cells exposed to oxidative stress. Apoptosis 2: 1-11.
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Typ dokumentu

Bibliografia

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Identyfikator YADDA

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