TY  - THES
AB  - Copper is essential for cellular function, but excess copper is toxic, requiring tight regulation through copper‑binding proteins and the ATP7A and ATP7B transporters. While ATP7B’s role in hepatic copper export is well established, its functions in other tissues are less understood. This work examines ATP7B expression and trafficking in the human large intestine and ovary. In colonic epithelial cells, ATP7B localizes apically and undergoes copper‑dependent trafficking, supporting a model in which excess copper is packaged into vesicles and excreted into the intestinal lumen. Additionally, using cisplatin‑resistant A2780‑CP20 cells, we show that ATP7B does not traffic in response to copper or cisplatin, suggesting that resistance arises from intracellular binding and sequestration rather than ATP7B‑mediated drug efflux.
AD  - Oregon Health and Science University
AU  - Zuzel, Vesna
DA  - 2010
DO  - 10.6083/M41834GZ
DO  - DOI
ED  - Lutsenko, Svetlana
ED  - Mentor
ID  - 556
KW  - Intestines
KW  - Adenosine Triphosphatases
KW  - Ovary
KW  - Homeostasis
KW  - Ovarian Neoplasms
KW  - Copper
L1  - https://digitalcollections.ohsu.edu/record/556/files/557_etd.pdf
L2  - https://digitalcollections.ohsu.edu/record/556/files/557_etd.pdf
L4  - https://digitalcollections.ohsu.edu/record/556/files/557_etd.pdf
LK  - https://digitalcollections.ohsu.edu/record/556/files/557_etd.pdf
N2  - Copper is essential for cellular function, but excess copper is toxic, requiring tight regulation through copper‑binding proteins and the ATP7A and ATP7B transporters. While ATP7B’s role in hepatic copper export is well established, its functions in other tissues are less understood. This work examines ATP7B expression and trafficking in the human large intestine and ovary. In colonic epithelial cells, ATP7B localizes apically and undergoes copper‑dependent trafficking, supporting a model in which excess copper is packaged into vesicles and excreted into the intestinal lumen. Additionally, using cisplatin‑resistant A2780‑CP20 cells, we show that ATP7B does not traffic in response to copper or cisplatin, suggesting that resistance arises from intracellular binding and sequestration rather than ATP7B‑mediated drug efflux.
PB  - Oregon Health and Science University
PY  - 2010
T1  - ATP7B expression and trafficking in the intestine and ovary: insights into specialized function
TI  - ATP7B expression and trafficking in the intestine and ovary: insights into specialized function
UR  - https://digitalcollections.ohsu.edu/record/556/files/557_etd.pdf
Y1  - 2010
ER  -