Akt confers cisplatin chemoresistance in human gynecological carcinoma cells by modulating PPM1D stability

Author:

Ali Ahmed Y.12,Kim Ji‐Young12,Pelletier Jean‐François34,Vanderhyden Barbara C.156,Bachvarov Dimcho R.34,Tsang Benjamin K.12578

Affiliation:

1. Department of Cellular & Molecular MedicineUniversity of OttawaOttawaOntarioCanada

2. Chronic Disease ProgramOttawa Hospital Research InstituteOttawaOntarioCanada

3. Département de Médecine MoleculaireFaculté de MédecineUniversité LavalQuébec CityQuébecCanada

4. Centre de Recherche du CHU de QuébecL'Hôtel‐Dieu de QuébecQuébec CityQuébecCanada

5. Department of Obstetrics & GynecologyUniversity of OttawaOttawaOntarioCanada

6. Centre for Cancer TherapeuticsOttawa Hospital Research InstituteOttawaOntarioCanada

7. Department of Interdisciplinary School of Health SciencesUniversity of OttawaOttawaOntarioCanada

8. World Class University (WCU) Biomodulation MajorDepartment of Agricultural BiotechnologyCollege of Agriculture and Life SciencesSeoul National UniversitySeoulRepublic of Korea

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Cancer Research,Molecular Biology

Reference66 articles.

1. www.cancer.ca/en/cancer‐information/cancer‐type/ovarian/statistics/?region =on. 2013.

2. Down‐regulation of X‐linked inhibitor of apoptosis protein induces apoptosis in chemoresistant human ovarian cancer cells;Sasaki H;Cancer Res,2000

3. Regulation of apoptosis-inducing factor-mediated, cisplatin-induced apoptosis by Akt

4. Akt promotes cisplatin resistance in human ovarian cancer cells through inhibition of p53 phosphorylation and nuclear function

5. Cisplatin Induces p53-Dependent FLICE-Like Inhibitory Protein Ubiquitination in Ovarian Cancer Cells

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