Українська English

ISSN 2522-9028 (Print)
ISSN 2522-9036 (Online)
DOI: https://doi.org/10.15407/fz

Fiziologichnyi Zhurnal

is a scientific journal issued by the

Bogomoletz Institute of Physiology
National Academy of Sciences of Ukraine

Editor-in-chief: V.F. Sagach

The journal was founded in 1955 as
1955 – 1977 "Fiziolohichnyi zhurnal" (ISSN 0015 – 3311)
1978 – 1993 "Fiziologicheskii zhurnal" (ISSN 0201 – 8489)
1994 – 2016 "Fiziolohichnyi zhurnal" (ISSN 0201 – 8489)
2017 – "Fiziolohichnyi zhurnal" (ISSN 2522-9028)

Fiziol. Zh. 2003; 49(6): 3-13

Effects of neuroendocrinedifferentiation of LNCaP cancer cells in human prostate on characteristics of volume–sensitive chloride current.

R.M. Lazarenko, Iu.M. Vitko, N.C. Pogorela, R.N. Skryma, Ia.M. Shuba

    А.А. Bogomoletz Institute of Physiology NationalAcademy of Sciences of Ukraine, Kiev



Abstract

The review presents a modern view on the functional – morphological peculiarities of 12 segments of the nephron canaliculi possessing some functional, biochemical and his- tologic distinctions that should be taken into account to study physiology, biochemistry, morphology and patho- physiology of the kidney.

Full text: (PDF, in Ukrainian)

References

  1. Alberts B., Bray D., Lewis J. et al. Molecular Biology of the Cell. – Garland Publishing. – 1994.
  2. Aprikian A.G., Cordon-Cardo C., Fair W.R., Reuter V.E. Characterization of neuroendocrine differentiation in human benign prostate and prostatic adenocarcinoma // Cancer. – 1993. – 71(12). – P. 3952 – 3965.
  3. Baquet A., Meijer A.J., Hue L. Hepatocyte swelling increases inositol 1,4,5-triphosphate, calcium and cyclic AMP concentration but antagonizes phosphorylase acti- vation by Ca2+ dependent hormones // FEBS lett. – 1991. 278. – P. 103 – 106.
  4. Bian X., Hudges F.M.Jr. , Huang Y.C.J.A., Putney J.W.Jr. Roles of cytoplasmic Ca2+ and intracellular Ca2+ stores in induction and suppression of apoptosis in S49 cells // Amer. J. Physiol. – 1997. – 272. – P. C1241 – C1249.
  5. Bonkhoff H. Neuroendocrine differentiation in human prostate cancer. Morphogenesis, proliferation and androgen receptor status // Ann. Oncol. – 2001. – 12. – P. 141 – 144.
  6. Bonkhoff H., Stein U., Remberger K. Multidirectional differentiation in the normal, hyperplastic, and neoplastic human prostate: simultaneous demonstration of cell-spe- cific epithelial markers // Hum. Pathol. – 1994. – 1. – P. 42 – 46.
  7. Bonkhoff H., Remberger K. Morphogenetic aspects of normal and abnormal prostatic growth // Pathol. Res. Pract. – 1995. – 191. – P. 833 – 835.
  8. Civan M.M., Coca-Prados M., Peterson-Yantorno K. Pathways signaling the regulatory volume decrease of cultured nonpigmented ciliary epithelial cells // Invest. Ophtalmol. Vis. Sci. – 1994. – 35. – P. 2876 – 2886.
  9. 9. Cox M.E., Deeble P.D., Lakhani S., Parsons S.J. Acquisition of neuroendocrine characteristics by prostate tumor cells is reversible: implications for prostate cancer progression // Cancer. Res. – 1999. – 59. – P. 3821 – 3830.
  10. 10. Cox M.E., Deeble P.D., Bissonette E.A., Parsons S.J. Activated 3',5'-cyclic AMP-dependent protein kinase is sufficient to induce neuroendocrine-like differentiation of the LNCaP prostate tumor cell line // J. Biol. Chem. – 2000. – 275(18). – P. 13812 – 13818.
  11. di Sant’Agnese P.A. Neuroendocrine differentiation in carcinoma of the prostate. Diagnostic, prognostic, and therapeutic implications // Cancer. – 1992. – 70. – P. 254 – 268.
  12. di Sant’Agnese P.A. Neuroendocrine cells of the prostate and neuroendocrine differentiation in prostatic carcinoma: a review of morphologic aspects // Urology. – 1998. – 51. – P. 121 – 124.
  13. Duan D., Zhong J., Hermoso M. et al. Functional inhibition of native volume-sensitive outwardly rectifying anion channels in muscle cells and Xenopus oocytes by anti-ClC-3 antibody // J. Physiol. – 2001. – 531. – P. 437 – 444.
  14. Eggermont J., Trouet D., Carton I., Nilius B. Cellular function and control of volume-regulated anion channels // Cell. Biochem. Biophys. – 2001. – 35. – P. 263 – 274.
  15. Foyouzi-Youssefi R., Arnaudeau S., Krause K.H. et al. Bcl-2 decreases the free Ca2+ concentration within the endoplasmic reticulum // Proc. Natl. Acad. Sci. USA. – 2000. – 97(11). – P. 5723 – 5728.
  16. Furuya Y., Lundmo P., Short A.D. et al. The role of calcium, pH, and cell proliferation in the programmed (apoptotic) death of androgen-independent prostatic cancer cells induced by thapsigargin // Cancer. Res. – 1994. – 54. – P. 6167 – 6175.
  17. Gkonos P.J., Lokeshwar B.L., Balkan W., Roos B.A. Neuroendocrine peptides stimulate adenyl cyclase in normal and malignant prostate cells // Regul. Pept. – 1995. – 59(1). – P. 43 – 51.
  18. He H., Lam M., McCormick T.S., Distelhorst C.W. Main- tenance of calcium homeostasis in the endoplasmic reticulum by Bcl-2 // J. Cell. Biol. – 1997. – 138(6). – P. 1219 – 1228.
  19. 19. Henson J.H. Relationships between the actin cytoskeleton and cell volume regulation // Microsc. Res. Tech. – 1999. – 47. – P. 155 – 162.
  20. 20. Ito T., Yamamoto S., Ohno Y. et al. Up-regulation of neuroendocrine differentiation in prostate cancer after androgen deprivation therapy, degree and androgen independence // Oncol. Rep. – 2001. – 8. – P. 1221 – 1224.
  21. July L.V., Akbari M., Zellweger T. et al. Clusterin expression is significantly enhanced in prostate cancer cells following androgen withdrawal therapy // Prostate. – 2002. – 50. – P. 179 – 188.
  22. Lemonnier L., Prevarskaya N., Shuba Y. et al. Ca2+ modulation of volume-regulated anion channels: evidence for colocalization with store-operated channels // FASEB J. – 2002. – 16. – P. 222 – 224.
  23. Levitan I., Almonte C. , Mollard P., Garber S.S. Modulation of a volume-regulated chloride current by F-actin // J. Membr. Biol. – 1995. – 147(3). – P. 283 – 294.
  24. Lodish H., Berk A., Zipursky S. et al. In: Molecular Cell. Bilolgy. 4th.ed. Ch. 18.1 The Actin Cytoskeleton. – 2000.
  25. Mariot P., Vanoverberghe K., Lalevee N. et al. Overexpression of an alpha 1H (Cav3.2) T-type calcium channel during neuroendocrine differentiation of human prostate cancer cells // J. Biol. Chem. – 2002. – 277. – P. 10824 – 10833.
  26. Mills J.W., Lubin M. Effect of adenosine 3',5'-cyclic monophosphate on volume and cytoskeleton of MDCK cells // Amer. J. Physiol. – 1986. – 250. – P. C319 – C324.
  27. Mills J.W. The cell cytoskeleton: possible role in volume control // Curr. Top. Membr. Transp. – 1987. – 30. – P. 75 – 101.
  28. Nilius B., Droogmans G. Amazing chloride channels: an overview // Acta. Physiol. Scand. – 2003. – 177. – P. 119-147.
  29. 29. Okada Y., Kubo M., Oiki S. et al. Properties of volume- sensitive Cl- channels in a human epithelial cell line // 1994. – Jpn. J. Physiol. – P. S31 – S35.
  30. 30. Okada Y. Volume expansion-sensing outward-rectifier Cl- channel: fresh start to the molecular identity and volume sensor // Amer. J. Physiol. – 1997. – 273. – P. С755 – С789.
  31. Okada Y., Maeno E. Apoptosis, cell volume regulation and volume-regulatory chloride channels // Comp. Biochem. Physiol. A Mol. Integr. Physiol. – 2001. – 130. – P. 377 – 383.
  32. Okada Y., Maeno E., Shimizu T. et al. Receptor-mediated control of regulatory volume decrease (RVD) and apoptotic volume decrease (AVD) // J. Physiol. – 2001. – 532. – P. 3 – 16.
  33. Pinton P., Ferrari D., Magalhaes P. et al. Reduced loading of intracellular Ca2+ stores and downregulation of capacitative Ca2+ influx in Bcl-2-overexpressing cells // J. Cell. Biol. – 2000. – 148. – P. 857 – 862.
  34. Raffo A.J., Perlman H. , Chen M.W. et al. Overexpression of bcl-2 protects prostate cancer cells from apoptosis in vitro and confers resistance to androgen depletion in vivo // Cancer. Res. – 1995. – 55. – P. 4438 – 4445.
  35. Shuba Y.M., Prevarskaya N., Lemonnier L. et al. Volumeregulated chloride conductance in the LNCaP human prostate cancer cell line // Amer. J. Physiol. – 2000. – 279. – P. C1144 – C1154.
  36. Skryma R., Mariot P., Bourhis X.L. et al. Store depletion and store-operated Ca2+ current in human prostate cancer LNCaP cells: involvement in apoptosis // J. Physiol. – 2000. – 527. – P. 71 – 83.
  37. Vanden Abeele F., Skryma R., Shuba Y. et al. Bcl-2-dependent modulation of Ca2+ homeostasis and store-operated chan- nels in prostate cancer cells // Cancer. Cell. – 2002. – 1. – P. 169 – 179.
  38. Wang H.G., Pathan N., Ethell I.M. et al. Ca2+-induced apoptosis through calcineurin dephosphorylation of BAD // Science. – 1999. – 284. – P. 339 – 343.
  39. 39. Watson P.A. Direct stimulation of adenylate cyclase by mechanical forces in S49 mouse lymphoma cells during hyposmotic swelling // J. Biol. Chem. – 1990. – 265. – P. 6569 – 6575.
  40. 40. Xing N., Qian J., Bostwick D. et al. Neuroendocrine cellsin human prostate over-express the anti-apoptosis protein survivin // Prostate. – 2001. – 48. – P. 7 – 15.
  41. Xue Y., Verhofstad A., Lange W. et al. Prostatic neuro- endocrine cells have a unique keratin expression pattern and do not express Bcl-2: cell kinetic features of neuroendocrine cells in the human prostate // Amer. J. Pathol. – 1997. – 151. – P. 1759 – 1765.
© National Academy of Sciences of Ukraine, Bogomoletz Institute of Physiology, 2014-2024.