Navitoclax combined with Alpelisib effectively inhibits Merkel cell carcinoma cell growth in vitro. (December 2020)
- Record Type:
- Journal Article
- Title:
- Navitoclax combined with Alpelisib effectively inhibits Merkel cell carcinoma cell growth in vitro. (December 2020)
- Main Title:
- Navitoclax combined with Alpelisib effectively inhibits Merkel cell carcinoma cell growth in vitro
- Authors:
- Chteinberg, Emil
Wetzels, Suzan
Gerritsen, Wouter
Temmerman, Lieve
van den Oord, Joost
Biessen, Erik
Kurz, Anna Kordelia
Winnepenninckx, Véronique
Zenke, Martin
Speel, Ernst-Jan
Hausen, Axel zur - Abstract:
- Background: Merkel cell carcinoma (MCC) is a highly malignant skin cancer. Despite major treatment improvements during the last decade, up to 50% of patients do not respond to therapy or develop recurrent disease. For these patients, alternative treatment options are urgently needed. Here, we assessed the efficacy of the combination of the BCL-2 inhibitor Navitoclax and the PI3K p110α inhibitor Alpelisib in MCC cell lines. Methods: The expression of BCL-2 was assessed by immunohistochemistry in MCC and MCC cell lines. Treatment with Navitoclax and Alpelisib alone and in combination was performed on four MCC cell lines. The decrease of cell viability during treatment was assessed by XTT assay and visualized for the combinations by 3D combinatorial index plotting. The increase of apoptotic cells was determined by cleaved PARP Western blotting and Annexin V staining. Results: Some 94% of MCCs and all three MCPyV-positive cell lines showed BCL-2 expression. Navitoclax monotreatment was shown to be highly effective when treating BCL-2-positive cell lines (IC50 -values ranging from 96.0 to 323.0 nM). The combination of Alpelisib and Navitoclax resulted in even stronger synergistic and prolonged inhibitions of MCC cell viability through apoptosis up to 4 days. Discussion: Our results show that the anti-apoptotic BCL-2 is frequently expressed in MCC and MCC cell lines. Inhibition of BCL-2 by Navitoclax in combination with Alpelisib revealed a strong synergy and prolonged inhibitionBackground: Merkel cell carcinoma (MCC) is a highly malignant skin cancer. Despite major treatment improvements during the last decade, up to 50% of patients do not respond to therapy or develop recurrent disease. For these patients, alternative treatment options are urgently needed. Here, we assessed the efficacy of the combination of the BCL-2 inhibitor Navitoclax and the PI3K p110α inhibitor Alpelisib in MCC cell lines. Methods: The expression of BCL-2 was assessed by immunohistochemistry in MCC and MCC cell lines. Treatment with Navitoclax and Alpelisib alone and in combination was performed on four MCC cell lines. The decrease of cell viability during treatment was assessed by XTT assay and visualized for the combinations by 3D combinatorial index plotting. The increase of apoptotic cells was determined by cleaved PARP Western blotting and Annexin V staining. Results: Some 94% of MCCs and all three MCPyV-positive cell lines showed BCL-2 expression. Navitoclax monotreatment was shown to be highly effective when treating BCL-2-positive cell lines (IC50 -values ranging from 96.0 to 323.0 nM). The combination of Alpelisib and Navitoclax resulted in even stronger synergistic and prolonged inhibitions of MCC cell viability through apoptosis up to 4 days. Discussion: Our results show that the anti-apoptotic BCL-2 is frequently expressed in MCC and MCC cell lines. Inhibition of BCL-2 by Navitoclax in combination with Alpelisib revealed a strong synergy and prolonged inhibition of MCC cell viability and induction of apoptosis. The combination of Navitoclax and Alpelisib is a novel potential treatment option for MCC patients. … (more)
- Is Part Of:
- Therapeutic advances in medical oncology. Volume 12(2020)
- Journal:
- Therapeutic advances in medical oncology
- Issue:
- Volume 12(2020)
- Issue Display:
- Volume 12, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 12
- Issue:
- 2020
- Issue Sort Value:
- 2020-0012-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-12
- Subjects:
- apoptosis -- BCL-2 inhibitor -- Merkel cell carcinoma -- Merkel cell polyomavirus -- PI3K inhibitor
Oncology -- Periodicals
Cancer -- Treatment -- Periodicals
616.994005 - Journal URLs:
- http://www.uk.sagepub.com/home.nav ↗
http://tam.sagepub.com/ ↗ - DOI:
- 10.1177/1758835920975621 ↗
- Languages:
- English
- ISSNs:
- 1758-8340
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14387.xml