نتایج جستجو برای: ژن atp7b

تعداد نتایج: 16252  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه اصفهان - دانشکده علوم 1392

جذب مس از طریق دستگاه گوارش به دقت تنظیم شده نمی باشد ولی دفع مس از طریق صفرا به شدت تنظیم شده می-باشد و این کار توسط یک گروه از پروتئین های انتقال دهنده مس وابسته به atp از جمله atp7b صورت می گیرد. این پروتئین توسط ژن atp7b برروی بازوی بلند کروموزوم 13 رمز می شود. کمبود این پروتئین باعث تجمع مس و بروز بیماری ویلسون می شود. بیماری ویلسون یک بیماری کبدی است که اغلب با علائم عصبی همراه می باشد و ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Kuniyuki Katano Roohangiz Safaei Goli Samimi Alison Holzer Mika Tomioka Murray Goodman Stephen B Howell

Some cisplatin (DDP)-resistant cells overexpress the copper export transporter ATP7B, and cells molecularly engineered to overexpress ATP7B are resistant to DDP. The interaction of Cu with ATP7B normally triggers its relocalization from the perinuclear region to more peripheral vesicles. To investigate the interaction of DDP with ATP7B, we examined the effect of DDP on the subcellular localizat...

Journal: :Oncology reports 2008
Tomoki Nakagawa Yoshimasa Inoue Hiroko Kodama Hitoshi Yamazaki Kenji Kawai Hiroshi Suemizu Ryota Masuda Masayuki Iwazaki Shunsuke Yamada Yoshito Ueyama Hiroshi Inoue Masato Nakamura

Copper-transporting P-type adenosine triphosphatase (ATP7B) is reportedly associated with platinum drug resistance in various solid carcinomas. However, the impact of ATP7B on platinum drug resistance in non-small cell lung cancer (NSCLC) remains unknown. We investigated ATP7B expression in nine human NSCLC xenografts using real-time polymerase chain reaction (PCR) and immunohistochemistry, and...

Journal: :Molecular pharmacology 2008
Roohangiz Safaei Shinji Otani Barrett J Larson Michael L Rasmussen Stephen B Howell

ATP7B is a P-type ATPase that mediates the efflux of copper. Recent studies have demonstrated that ATP7B regulates the cellular efflux of cisplatin (DDP) and controls sensitivity to the cytotoxic effects of this drug. To determine whether DDP is a substrate for ATP7B, DDP transport was assayed in vesicles isolated from Sf9 cells infected with a baculovirus that expressed either the wild-type AT...

Journal: :Molecular pharmacology 2003
Kuniyuki Katano Roohangiz Safaei Goli Samimi Alison Holzer Myriam Rochdi Stephen B Howell

Human tumor cells lines with acquired resistance to cisplatin (DDP) and carboplatin (CBDCA) are often cross-resistant to copper and vice versa, and some DDP-resistant cells overexpress the copper export pump ATP7B. We sought to demonstrate that ATP7B directly mediates resistance to DDP and CBDCA by stably transfecting human carcinoma cells with a vector designed to express ATP7B. Increased expr...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Kentaro Nakayama Atsuko Kanzaki Kunihiko Terada Masato Mutoh Kenji Ogawa Toshihiro Sugiyama Seiichi Takenoshita Kiyoshi Itoh Nobuo Yaegashi Kohji Miyazaki Nouri Neamati Yuji Takebayashi

PURPOSE A major obstacle in the treatment of ovarian carcinoma is the intrinsic/acquired resistance to cisplatin-based chemotherapy. Cu-transporting ATPase (ATP7B) has been reported to be associated with cisplatin resistance in vitro. However, the clinical significance of this transporter has not previously been addressed. Our goal was to investigate ATP7B expression in ovarian carcinoma and wh...

Journal: :Journal of cell science 2016
Vasiliki Lalioti Ramón Peiró Manuela Pérez-Berlanga Yo Tsuchiya Angeles Muñoz Teresa Villalba Carlos Sanchez Ignacio V Sandoval

The Cu(+) pump ATP7B plays an irreplaceable role in the elimination of excess Cu(+) by the hepatocyte into the bile. The trafficking and site of action of ATP7B are subjects of controversy. One current proposal is that an increase in intracellular Cu(+) results in the translocation of ATP7B to the lysosomes and excretion of excess Cu(+) through lysosomal-mediated exocytosis at the bile canalicu...

Journal: :European journal of histochemistry : EJH 2005
D Fanni L Pilloni S Orrù P Coni C Liguori S Serra M L Lai A Uccheddu L Contu P Van Eyken G Faa

ATP7B is a copper transporting P-type ATPase, also known as Wilson disease protein, which plays a key role in copper distribution inside cells. Recent experimental data in cell culture have shown that ATP7B putatively serves a dual function in hepatocytes: when localized to the Golgi apparatus, it has a biosynthetic role, delivering copper atoms to apoceruloplasmin; when the hepatocytes are und...

2014
Elena V. Polishchuk Mafalda Concilli Simona Iacobacci Giancarlo Chesi Nunzia Pastore Pasquale Piccolo Simona Paladino Daniela Baldantoni Sven C.D. van IJzendoorn Jefferson Chan Christopher J. Chang Angela Amoresano Francesca Pane Piero Pucci Antonietta Tarallo Giancarlo Parenti Nicola Brunetti-Pierri Carmine Settembre Andrea Ballabio Roman S. Polishchuk

Copper is an essential yet toxic metal and its overload causes Wilson disease, a disorder due to mutations in copper transporter ATP7B. To remove excess copper into the bile, ATP7B traffics toward canalicular area of hepatocytes. However, the trafficking mechanisms of ATP7B remain elusive. Here, we show that, in response to elevated copper, ATP7B moves from the Golgi to lysosomes and imports me...

2016
F M Moinuddin Yoshinari Shinsato Masaharu Komatsu Ryoichi Mitsuo Kentaro Minami Masatatsu Yamamoto Kohich Kawahara Hirofumi Hirano Kazunori Arita Tatsuhiko Furukawa

We previously reported that ATP7B is involved in cisplatin resistance and ATP7A confers multidrug resistance (MDR) in cancer cells.In this study, we show that ATP7B expressing cells also are resistant to doxorubicin, SN-38, etoposide, and paclitaxel as well as cisplatin.In ATP7B expressing cells, doxorubicin relocated from the nuclei to the late-endosome at 4 hours after doxorubicin exposure. E...

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