Navigation überspringen
Universitätsbibliothek Heidelberg
Status: Bibliographieeintrag

Verfügbarkeit
Standort: ---
Exemplare: ---
heiBIB
 Online-Ressource
Verfasst von:Shahmoradgoli, Maria [VerfasserIn]   i
 Riazalhosseini, Yasser [VerfasserIn]   i
 Haag, Daniel [VerfasserIn]   i
 Becker, Natalia [VerfasserIn]   i
 Hovestadt, Volker [VerfasserIn]   i
 Heck, Stefanie [VerfasserIn]   i
 Sinn, Peter [VerfasserIn]   i
 Schneeweiss, Andreas [VerfasserIn]   i
 Mannherz, Otto [VerfasserIn]   i
 Şahin, Özgür [VerfasserIn]   i
 Lichter, Peter [VerfasserIn]   i
Titel:Protein phosphatase 1, regulatory subunit 15B is a survival factor for ERα-positive breast cancer
Verf.angabe:Maria Shahmoradgoli, Yasser Riazalhosseini, Daniel Haag, Natalia Becker, Volker Hovestadt, Stefanie Heck, Hans-Peter Sinn, Andreas Schneeweiss, Otto Mannherz, Özgür Sahin and Peter Lichter
Jahr:2013
Umfang:6 S.
Teil:volume:132
 year:2013
 number:11
 pages:2714-2719
 extent:6
Fussnoten:Online 20 Nov 2012 ; Gesehen am 19.08.2021
Titel Quelle:Enthalten in: International journal of cancer
Ort Quelle:Bognor Regis : Wiley-Liss, 1966
Jahr Quelle:2013
Band/Heft Quelle:132(2013), 11, Seite 2714-2719
ISSN Quelle:1097-0215
Abstract:Breast cancer is a heterogeneous disease at both the clinical and molecular levels. This heterogeneity may give rise to different therapy responses. Molecular profiling has facilitated identification of signatures for stratifying patients who would potentially benefit from given therapies. Previously, we reported on a subset of genes with the potential for predicting response of primary breast cancer to neoadjuvant chemotherapy. Herein, we report that patients with luminal (estrogen receptor α [ERα]-expressing) breast cancer were enriched for nonresponders. To identify novel factors that contribute to the survival of breast cancer cells, a loss-of-function screen was performed with a subset of genes overexpressed in patients with disease resistant to chemotherapy. This approach led us to identify protein phosphatase 1, regulatory subunit 15B (PPP1R15B) as a factor with a potentially essential role in the survival of ERα-positive breast cancer cells. Functional analyses showed that PPP1R15B depletion results in impaired proliferation due to unsuccessful transition of cells from G1 to S phase of the cell cycle, and apoptosis induction. Moreover, our data revealed a regulatory role for PPP1R15B in activating ERα. Furthermore, a high level of PPP1R15B mRNA expression was associated with poor outcome following tamoxifen-based therapy. Accordingly, knockdown of PPP1R15B expression sensitized tamoxifen-resistant MCF-7 breast cancer cells to tamoxifen while reducing ERα abundance in these cells. Our findings reveal a novel role for PPP1R15B in the survival and therapy response of ERα-positive breast cancer and may open new avenues for tumor subtype-specific therapeutic strategies in the era of personalized medicine.
DOI:doi:10.1002/ijc.27945
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1002/ijc.27945
 Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.27945
 DOI: https://doi.org/10.1002/ijc.27945
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:breast cancer
 cell proliferation
 drug resistance
 estrogen receptor α
 PPP1R15B
 tamoxifen
K10plus-PPN:1767440359
Verknüpfungen:→ Zeitschrift

Permanenter Link auf diesen Titel (bookmarkfähig):  https://katalog.ub.uni-heidelberg.de/titel/68772196   QR-Code
zum Seitenanfang