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Evaluating anti-tumor activity of palbociclib plus radiation in anaplastic and radiation-induced meningiomas: pre-clinical investigations

Purpose Meningiomas are common brain tumors, the majority of which are considered benign. Despite surgery and/or radiation therapy, recurrence rates are approximately 8–10%. One likely cause is the dysregulation of cyclin d -cyclin-dependent kinases 4 and 6 (CDK4/6)-retinoblastoma (Rb) pathway, whic...

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Published in:Clinical & translational oncology 2020-11, Vol.22 (11), p.2017-2025
Main Authors: Das, A., Alshareef, M., Martinez Santos, J. L., Porto, G. B. F., McDonald, D. G., Infinger, L. K., Vandergrift, W. A., Lindhorst, S. M., Varma, A. K., Patel, S. J., Cachia, D.
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cites cdi_FETCH-LOGICAL-c462t-8aecefb93195f12b0064afa3d96f1faeaa968314533bae9de39f644f4d6b17103
container_end_page 2025
container_issue 11
container_start_page 2017
container_title Clinical & translational oncology
container_volume 22
creator Das, A.
Alshareef, M.
Martinez Santos, J. L.
Porto, G. B. F.
McDonald, D. G.
Infinger, L. K.
Vandergrift, W. A.
Lindhorst, S. M.
Varma, A. K.
Patel, S. J.
Cachia, D.
description Purpose Meningiomas are common brain tumors, the majority of which are considered benign. Despite surgery and/or radiation therapy, recurrence rates are approximately 8–10%. One likely cause is the dysregulation of cyclin d -cyclin-dependent kinases 4 and 6 (CDK4/6)-retinoblastoma (Rb) pathway, which controls the cell cycle restriction point. This pathway is commonly dysregulated in anaplastic meningioma cell lines (AM) and radiation-induced meningioma cells (RIM), making it a rational target for anti-meningioma therapy. In this study, we investigate the effect of a CDK4/6 inhibitor, palbociclib, with radiation in relevant pre-clinical models. Methods In vitro cell culture, ex vivo slice culture and in vivo cell line-derived orthotopic xenograft animal models of AM/RIM were utilized to assess treatment efficacy with palbociclib plus radiation. Treatment effects were examined by immunoblot, cell viability, apoptosis, and cell cycle progression. Results The in vitro and ex vivo studies demonstrate that palbociclib plus radiation treatment reduced proliferation and has additional effects on cell cycling, including induction of an RB-associated G (1) arrest in Rb+ AM and RIM cells, but not in Rb− cells. Our results also demonstrated reduced CDK4 and CDK6 expression as well as reduced E2F target gene expression (CCNA2 and CCNE2) with the combination therapy. MRI results in vivo demonstrated reduced tumor size at 5 weeks when treated with 14 days palbociclib (10 mg/kg) plus 6 Gy radiation compared to saline-treated tumors. Finally, no hepatic toxicity was found after treatments. Conclusion A pre-clinical murine model provides preclinical evidence for use of palbociclib plus radiation as a therapeutic agent for Rb+ meningiomas.
doi_str_mv 10.1007/s12094-020-02341-7
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L. ; Porto, G. B. F. ; McDonald, D. G. ; Infinger, L. K. ; Vandergrift, W. A. ; Lindhorst, S. M. ; Varma, A. K. ; Patel, S. J. ; Cachia, D.</creator><creatorcontrib>Das, A. ; Alshareef, M. ; Martinez Santos, J. L. ; Porto, G. B. F. ; McDonald, D. G. ; Infinger, L. K. ; Vandergrift, W. A. ; Lindhorst, S. M. ; Varma, A. K. ; Patel, S. J. ; Cachia, D.</creatorcontrib><description>Purpose Meningiomas are common brain tumors, the majority of which are considered benign. Despite surgery and/or radiation therapy, recurrence rates are approximately 8–10%. One likely cause is the dysregulation of cyclin d -cyclin-dependent kinases 4 and 6 (CDK4/6)-retinoblastoma (Rb) pathway, which controls the cell cycle restriction point. This pathway is commonly dysregulated in anaplastic meningioma cell lines (AM) and radiation-induced meningioma cells (RIM), making it a rational target for anti-meningioma therapy. In this study, we investigate the effect of a CDK4/6 inhibitor, palbociclib, with radiation in relevant pre-clinical models. Methods In vitro cell culture, ex vivo slice culture and in vivo cell line-derived orthotopic xenograft animal models of AM/RIM were utilized to assess treatment efficacy with palbociclib plus radiation. Treatment effects were examined by immunoblot, cell viability, apoptosis, and cell cycle progression. Results The in vitro and ex vivo studies demonstrate that palbociclib plus radiation treatment reduced proliferation and has additional effects on cell cycling, including induction of an RB-associated G (1) arrest in Rb+ AM and RIM cells, but not in Rb− cells. Our results also demonstrated reduced CDK4 and CDK6 expression as well as reduced E2F target gene expression (CCNA2 and CCNE2) with the combination therapy. MRI results in vivo demonstrated reduced tumor size at 5 weeks when treated with 14 days palbociclib (10 mg/kg) plus 6 Gy radiation compared to saline-treated tumors. Finally, no hepatic toxicity was found after treatments. 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J.</au><au>Cachia, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluating anti-tumor activity of palbociclib plus radiation in anaplastic and radiation-induced meningiomas: pre-clinical investigations</atitle><jtitle>Clinical &amp; translational oncology</jtitle><stitle>Clin Transl Oncol</stitle><addtitle>Clin Transl Oncol</addtitle><date>2020-11-01</date><risdate>2020</risdate><volume>22</volume><issue>11</issue><spage>2017</spage><epage>2025</epage><pages>2017-2025</pages><issn>1699-048X</issn><eissn>1699-3055</eissn><abstract>Purpose Meningiomas are common brain tumors, the majority of which are considered benign. Despite surgery and/or radiation therapy, recurrence rates are approximately 8–10%. One likely cause is the dysregulation of cyclin d -cyclin-dependent kinases 4 and 6 (CDK4/6)-retinoblastoma (Rb) pathway, which controls the cell cycle restriction point. This pathway is commonly dysregulated in anaplastic meningioma cell lines (AM) and radiation-induced meningioma cells (RIM), making it a rational target for anti-meningioma therapy. In this study, we investigate the effect of a CDK4/6 inhibitor, palbociclib, with radiation in relevant pre-clinical models. Methods In vitro cell culture, ex vivo slice culture and in vivo cell line-derived orthotopic xenograft animal models of AM/RIM were utilized to assess treatment efficacy with palbociclib plus radiation. Treatment effects were examined by immunoblot, cell viability, apoptosis, and cell cycle progression. Results The in vitro and ex vivo studies demonstrate that palbociclib plus radiation treatment reduced proliferation and has additional effects on cell cycling, including induction of an RB-associated G (1) arrest in Rb+ AM and RIM cells, but not in Rb− cells. Our results also demonstrated reduced CDK4 and CDK6 expression as well as reduced E2F target gene expression (CCNA2 and CCNE2) with the combination therapy. MRI results in vivo demonstrated reduced tumor size at 5 weeks when treated with 14 days palbociclib (10 mg/kg) plus 6 Gy radiation compared to saline-treated tumors. Finally, no hepatic toxicity was found after treatments. 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title Evaluating anti-tumor activity of palbociclib plus radiation in anaplastic and radiation-induced meningiomas: pre-clinical investigations
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