Literature DB >> 27370604

Combination of Imatinib Mesylate and AKT Inhibitor Provides Synergistic Effects in Preclinical Study of Gastrointestinal Stromal Tumor.

Phillip Zook1, Harsh B Pathak2, Martin G Belinsky1, Lawrence Gersz1, Karthik Devarajan3, Yan Zhou3, Andrew K Godwin2, Margaret von Mehren1, Lori Rink1.   

Abstract

PURPOSE: Gastrointestinal stromal tumors (GIST) generally harbor activating mutations in the receptor tyrosine kinase KIT or in the related platelet-derived growth factor receptor alpha (PDGFRA). GIST treated with imatinib mesylate or second-line therapies that target mutant forms of these receptors generally escape disease control and progress over time. Inhibiting additional molecular targets may provide more substantial disease control. Recent studies have implicated the PI3K/AKT pathway in the survival of imatinib mesylate-resistant GIST cell lines and tumors. EXPERIMENTAL
DESIGN: Here, we performed in vitro and in vivo studies evaluating the novel combination of imatinib mesylate with the AKT inhibitor MK-2206 in GIST. Whole-transcriptome sequencing (WTS) of xenografts was performed to explore the molecular aspects of tumor response to this novel combination and to potentially identify additional therapeutic targets in GIST.
RESULTS: This drug combination demonstrated significant synergistic effects in a panel of imatinib mesylate-sensitive and -resistant GIST cell lines. Furthermore, combination therapy provided significantly greater efficacy, as measured by tumor response and animal survival, in imatinib mesylate-sensitive GIST xenografts as compared with treatment with imatinib mesylate or MK-2206 alone. WTS implicated two neural genes, brain expressed X-linked 1 and neuronal pentraxin I, whose expression was significantly upregulated in combination-treated tumors compared with tumors treated with the two monotherapies.
CONCLUSIONS: These studies provide strong preclinical justification for combining imatinib mesylate with an AKT inhibitor as a front-line therapy in GIST. In addition, the WTS implicated the BCL-2/BAX/BAD apoptotic pathway as a potential mechanism for this enhanced combination effect. Clin Cancer Res; 23(1); 171-80. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27370604      PMCID: PMC5203981          DOI: 10.1158/1078-0432.CCR-16-0529

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  46 in total

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2.  A potent combination of the novel PI3K Inhibitor, GDC-0941, with imatinib in gastrointestinal stromal tumor xenografts: long-lasting responses after treatment withdrawal.

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Journal:  Clin Cancer Res       Date:  2012-12-11       Impact factor: 12.531

3.  STI571 inactivation of the gastrointestinal stromal tumor c-KIT oncoprotein: biological and clinical implications.

Authors:  D A Tuveson; N A Willis; T Jacks; J D Griffin; S Singer; C D Fletcher; J A Fletcher; G D Demetri
Journal:  Oncogene       Date:  2001-08-16       Impact factor: 9.867

4.  The phosphatase and tensin homolog regulates epidermal growth factor receptor (EGFR) inhibitor response by targeting EGFR for degradation.

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5.  Long-term results from a randomized phase II trial of standard- versus higher-dose imatinib mesylate for patients with unresectable or metastatic gastrointestinal stromal tumors expressing KIT.

Authors:  Charles D Blanke; George D Demetri; Margaret von Mehren; Michael C Heinrich; Burton Eisenberg; Jonathan A Fletcher; Christopher L Corless; Christopher D M Fletcher; Peter J Roberts; Daniela Heinz; Elisabeth Wehre; Zariana Nikolova; Heikki Joensuu
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Review 6.  Clinical and molecular characteristics of gastrointestinal stromal tumors in the pediatric and young adult population.

Authors:  Lori Rink; Andrew K Godwin
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7.  Imatinib mesylate (STI-571 Glivec, Gleevec) is an active agent for gastrointestinal stromal tumours, but does not yield responses in other soft-tissue sarcomas that are unselected for a molecular target. Results from an EORTC Soft Tissue and Bone Sarcoma Group phase II study.

Authors:  J Verweij; A van Oosterom; J-Y Blay; I Judson; S Rodenhuis; W van der Graaf; J Radford; A Le Cesne; P C W Hogendoorn; E D di Paola; M Brown; O S Nielsen
Journal:  Eur J Cancer       Date:  2003-09       Impact factor: 9.162

8.  Evolutionary dynamics of cancer in response to targeted combination therapy.

Authors:  Ivana Bozic; Johannes G Reiter; Benjamin Allen; Tibor Antal; Krishnendu Chatterjee; Preya Shah; Yo Sup Moon; Amin Yaqubie; Nicole Kelly; Dung T Le; Evan J Lipson; Paul B Chapman; Luis A Diaz; Bert Vogelstein; Martin A Nowak
Journal:  Elife       Date:  2013-06-25       Impact factor: 8.140

9.  BEX1 acts as a tumor suppressor in acute myeloid leukemia.

Authors:  Oscar Lindblad; Tianfeng Li; Xianwei Su; Jianmin Sun; Nuzhat N Kabir; Fredrik Levander; Hui Zhao; Gang Lu; Lars Rönnstrand; Julhash U Kazi
Journal:  Oncotarget       Date:  2015-08-28

10.  BEX1 promotes imatinib-induced apoptosis by binding to and antagonizing BCL-2.

Authors:  Qian Xiao; Yeting Hu; Yue Liu; Zhanhuai Wang; Haitao Geng; Lifeng Hu; Dengyong Xu; Ke Wang; Lei Zheng; Shu Zheng; Kefeng Ding
Journal:  PLoS One       Date:  2014-03-13       Impact factor: 3.240

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  15 in total

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Journal:  Biochim Biophys Acta Rev Cancer       Date:  2016-12-05       Impact factor: 10.680

2.  Direct engagement of the PI3K pathway by mutant KIT dominates oncogenic signaling in gastrointestinal stromal tumor.

Authors:  Benedikt Bosbach; Ferdinand Rossi; Yasemin Yozgat; Jennifer Loo; Jennifer Q Zhang; Georgina Berrozpe; Katherine Warpinski; Imke Ehlers; Darren Veach; Andrew Kwok; Katia Manova; Cristina R Antonescu; Ronald P DeMatteo; Peter Besmer
Journal:  Proc Natl Acad Sci U S A       Date:  2017-09-18       Impact factor: 11.205

3.  Refining Prognosis in Localized Gastrointestinal Stromal Tumor: Clinical Significance of Phosphatase and Tensin Homolog Low Expression and Gene Loss.

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Review 4.  Development of Fangjiomics for Systems Elucidation of Synergistic Mechanism Underlying Combination Therapy.

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Journal:  Comput Struct Biotechnol J       Date:  2018-11-20       Impact factor: 7.271

Review 5.  The PTEN Tumor Suppressor Gene in Soft Tissue Sarcoma.

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Journal:  Cancers (Basel)       Date:  2019-08-14       Impact factor: 6.639

6.  Farnesiferol C Induces Apoptosis in Chronic Myelogenous Leukemia Cells as an Imatinib Sensitizer via Caspase Activation and HDAC (Histone Deacetylase) Inactivation.

Authors:  Ji Hoon Jung; Ji Eon Park; Deok Yong Sim; Eunji Im; Woon Yi Park; Duckgue Lee; Bum-Sang Shim; Sung-Hoon Kim
Journal:  Int J Mol Sci       Date:  2019-11-06       Impact factor: 5.923

7.  Inhibition of AKT-Signaling Sensitizes Soft Tissue Sarcomas (STS) and Gastrointestinal Stromal Tumors (GIST) to Doxorubicin via Targeting of Homology-Mediated DNA Repair.

Authors:  Sergei Boichuk; Firuza Bikinieva; Ilmira Nurgatina; Pavel Dunaev; Elena Valeeva; Aida Aukhadieva; Alexey Sabirov; Aigul Galembikova
Journal:  Int J Mol Sci       Date:  2020-11-22       Impact factor: 5.923

8.  Oncogene mutational analysis in Chinese gastrointestinal stromal tumor patients.

Authors:  Qiong Chen; Rong Li; Zhi-Gao Zhang; Qiao-Ting Deng; Kun Li; Hao Wang; Xue-Xi Yang; Ying-Song Wu
Journal:  Onco Targets Ther       Date:  2018-04-20       Impact factor: 4.147

9.  Imatinib in combination with phosphoinositol kinase inhibitor buparlisib in patients with gastrointestinal stromal tumour who failed prior therapy with imatinib and sunitinib: a Phase 1b, multicentre study.

Authors:  Hans Gelderblom; Robin L Jones; Suzanne George; Claudia Valverde Morales; Charlotte Benson; Daniel J Renouf; Toshihiko Doi; Axel Le Cesne; Michael Leahy; Sabine Hertle; Paola Aimone; Ulrike Brandt; Patrick Schӧffski
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Review 10.  Role of PI3K/AKT pathway in cancer: the framework of malignant behavior.

Authors:  Ningni Jiang; Qijie Dai; Xiaorui Su; Jianjiang Fu; Xuancheng Feng; Juan Peng
Journal:  Mol Biol Rep       Date:  2020-04-24       Impact factor: 2.742

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