VAŇHARA, Petr, Eva LINCOVÁ, Karel SOUČEK a Jan ŠMARDA. Regulation of osteoclast differentiation by the TGFbeta proteins secreted by prostate cancer. In Stem cells, cancer and aging. Singapore: Keystone symposia, International Society of Differentiation, 2008, s. 89-90.
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Základní údaje
Originální název Regulation of osteoclast differentiation by the TGFbeta proteins secreted by prostate cancer
Název česky Regulace osteoklastové diferenciaci proteiny TGFbeta sekretovanymi nadory prostaty
Autoři VAŇHARA, Petr, Eva LINCOVÁ, Karel SOUČEK a Jan ŠMARDA.
Vydání Singapore, Stem cells, cancer and aging, s. 89-90, 2008.
Nakladatel Keystone symposia, International Society of Differentiation
Další údaje
Originální jazyk angličtina
Typ výsledku Stať ve sborníku
Obor Genetika a molekulární biologie
Stát vydavatele Singapur
Utajení není předmětem státního či obchodního tajemství
Organizační jednotka Přírodovědecká fakulta
Klíčová slova anglicky TGF; GDF-15; BMP-7; TGFb1; prostate cancer; osteoclast
Štítky BMP-7, GDF-15, osteoclast, prostate cancer, TGF, TGFb1
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnil: prof. RNDr. Jan Šmarda, CSc., učo 1223. Změněno: 9. 7. 2010 10:55.
Anotace
Prostate caner is a common disease in western countries. Primary prostate tumors preferentially disseminate to bones. Homing and activity of cancer cells in the bone microenvironment as well as specific mechanisms used by tumor cells remain to be elucidated. This study aims to describe the effects of three members of TGFb protein family (TGFb, BMP-7 and GDF-15) on osteoclast differentiation of murine cell line RAW264.7. These proteins are secreted by prostate cancer cell line LNCaP, possess strong morphogenic effects and are supposed to influence bone microenvironment significantly. TGFb, BMP-7 or GDF-15 affected efficiency of osteoclast differentiation strongly. While TGFb treatment stimulated RANKL-induced differentiation, BMP-7 and GDF-15 cytokines clearly reduced differentiation potential of RAW264.7 cells to active osteoclasts. In contrast to RANKL/TGFb that induced expression of several osteoclast-associated genes, RANKL/GDF-15 and RANKL/BMP-7 suppressed it. According to these we document that different members of the TGFb protein family differently regulate signaling in osteoclasts and consequently modulate the final cellular answer.
Anotace česky
Prostate caner is a common disease in western countries. Primary prostate tumors preferentially disseminate to bones. Homing and activity of cancer cells in the bone microenvironment as well as specific mechanisms used by tumor cells remain to be elucidated. This study aims to describe the effects of three members of TGFb protein family (TGFb, BMP-7 and GDF-15) on osteoclast differentiation of murine cell line RAW264.7. These proteins are secreted by prostate cancer cell line LNCaP, possess strong morphogenic effects and are supposed to influence bone microenvironment significantly. TGFb, BMP-7 or GDF-15 affected efficiency of osteoclast differentiation strongly. While TGFb treatment stimulated RANKL-induced differentiation, BMP-7 and GDF-15 cytokines clearly reduced differentiation potential of RAW264.7 cells to active osteoclasts. In contrast to RANKL/TGFb that induced expression of several osteoclast-associated genes, RANKL/GDF-15 and RANKL/BMP-7 suppressed it. According to these we document that different members of the TGFb protein family differently regulate signaling in osteoclasts and consequently modulate the final cellular answer.
Návaznosti
GA301/06/0036, projekt VaVNázev: Úloha vybraných transkripčních faktorů v osteoklastové diferenciační dráze
Investor: Grantová agentura ČR, Úloha vybraných transkripčních faktorů v osteoklastové diferenciační dráze
GD204/08/H054, projekt VaVNázev: Molekulární mechanismy proliferace a diferenciace buněk
Investor: Grantová agentura ČR, Molekulární mechanismy proliferace a diferenciace buněk
MSM0021622415, záměrNázev: Molekulární podstata buněčných a tkáňových regulací
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Molekulární podstata buněčných a tkáňových regulací
VytisknoutZobrazeno: 25. 4. 2024 06:22