The HSP90 inhibitor ganetespib synergizes with the MET kinase inhibitor crizotinib in both crizotinib-sensitive and -resistant MET-driven tumor models.

Abstract:

:The proto-oncogene MET is aberrantly activated via overexpression or mutation in numerous cancers, making it a prime anticancer molecular target. However, the clinical success of MET-directed tyrosine kinase inhibitors (TKI) has been limited due, in part, to mutations in the MET kinase domain that confer therapeutic resistance. Circumventing this problem remains a key challenge to improving durable responses in patients receiving MET-targeted therapy. MET is an HSP90-dependent kinase, and in this report we show that HSP90 preferentially interacts with and stabilizes activated MET, regardless of whether the activation is ligand-dependent or is a consequence of kinase domain mutation. In contrast, many MET-TKI show a preference for the inactive form of the kinase, and activating mutations in MET can confer resistance. Combining the HSP90 inhibitor ganetespib with the MET-TKI crizotinib achieves synergistic inhibition of MET, its downstream signaling pathways, and tumor growth in both TKI-sensitive and -resistant MET-driven tumor models. These data suggest that inclusion of an HSP90 inhibitor can partially restore TKI sensitivity to previously resistant MET mutants, and they provide the foundation for clinical evaluation of this therapeutic combination in patients with MET-driven cancers.

journal_name

Cancer Res

journal_title

Cancer research

authors

Miyajima N,Tsutsumi S,Sourbier C,Beebe K,Mollapour M,Rivas C,Yoshida S,Trepel JB,Huang Y,Tatokoro M,Shinohara N,Nonomura K,Neckers L

doi

10.1158/0008-5472.CAN-13-1156

subject

Has Abstract

pub_date

2013-12-01 00:00:00

pages

7022-33

issue

23

eissn

0008-5472

issn

1538-7445

pii

0008-5472.CAN-13-1156

journal_volume

73

pub_type

杂志文章
  • Marked genetic differences between stage pTa and stage pT1 papillary bladder cancer detected by comparative genomic hybridization.

    abstract::Little is known about the genetic changes underlying invasive tumor growth in bladder cancer. Because alterations that are linked to invasive tumor growth may be detectable in minimally invasive (stage pT1) but not in noninvasive (stage pTa) tumors, we searched for genetic differences between 28 pTa and 28 papillary p...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Richter J,Jiang F,Görög JP,Sartorius G,Egenter C,Gasser TC,Moch H,Mihatsch MJ,Sauter G

    更新日期:1997-07-15 00:00:00

  • Role of cyclin D1 as a mediator of c-Met- and beta-catenin-induced hepatocarcinogenesis.

    abstract::Activation of c-Met signaling and beta-catenin mutations are frequent genetic events observed in liver cancer development. Recently, we demonstrated that activated beta-catenin can cooperate with c-Met to induce liver cancer formation in a mouse model. Cyclin D1 (CCND1) is an important cell cycle regulator that is con...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-08-2514

    authors: Patil MA,Lee SA,Macias E,Lam ET,Xu C,Jones KD,Ho C,Rodriguez-Puebla M,Chen X

    更新日期:2009-01-01 00:00:00

  • Topography of nonneoplastic and neoplastic cells of common origin.

    abstract::The possibility that neoplastic transformation may characteristically alter cell surface morphology prompted a comparison by scanning electron microscopy of nonneoplastic and tumorigenic cell lines from a single clone of mouse embryo cells. Among those studied by scanning electron microscopy, six lines of this clone p...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Wetzel B,Sanford KK,Fox CH,Jones GM,Westbrook EW,Tarone RE

    更新日期:1977-03-01 00:00:00

  • HDAC6 Inhibition Synergizes with Anti-PD-L1 Therapy in ARID1A-Inactivated Ovarian Cancer.

    abstract::ARID1A, encoding a subunit of the SWI/SNF complex, is the most frequently mutated epigenetic regulator in human cancers and is mutated in more than 50% of ovarian clear cell carcinomas (OCCC), a disease that currently has no effective therapy. Inhibition of histone deacetylase 6 (HDAC6) suppresses the growth of ARID1A...

    journal_title:Cancer research

    pub_type: 评论,杂志文章

    doi:10.1158/0008-5472.CAN-19-1302

    authors: Fukumoto T,Fatkhutdinov N,Zundell JA,Tcyganov EN,Nacarelli T,Karakashev S,Wu S,Liu Q,Gabrilovich DI,Zhang R

    更新日期:2019-11-01 00:00:00

  • Macrophage Blockade Using CSF1R Inhibitors Reverses the Vascular Leakage Underlying Malignant Ascites in Late-Stage Epithelial Ovarian Cancer.

    abstract::Malignant ascites is a common complication in the late stages of epithelial ovarian cancer (EOC) that greatly diminishes the quality of life of patients. Malignant ascites is a known consequence of vascular dysfunction, but current approved treatments are not effective in preventing fluid accumulation. In this study, ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-14-3373

    authors: Moughon DL,He H,Schokrpur S,Jiang ZK,Yaqoob M,David J,Lin C,Iruela-Arispe ML,Dorigo O,Wu L

    更新日期:2015-11-15 00:00:00

  • Temporal patterns of covalent DNA adducts in rat liver after single and multiple doses of aflatoxin B1.

    abstract::We examined patterns of covalent modifications of DNA produced in rat liver after exposure to single and multiple doses of aflatoxin B1. The principal product, previously identified as 2,3-dihydro-3-hydroxy(N7-guanyl) aflatoxin B1, was removed rapidly from liver DNA in vivo after a 0.6-mg/kg dose was administered i.p....

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Croy RG,Wogan GN

    更新日期:1981-01-01 00:00:00

  • Homo- and hetero-oligomerization of the c-Abl kinase and Abelson-interactor-1.

    abstract::Oligomerization of the nonreceptor tyrosine kinase c-Abl can activate its transforming potential. Domains mediating oligomerization within the BCR-ABL and TEL-ABL oncoproteins are required for transforming activity, and fusion of inducible dimerization domains to c-Abl can generate chimeric proteins with dimerization-...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Fan PD,Cong F,Goff SP

    更新日期:2003-02-15 00:00:00

  • NKR-P1+ cells localize selectively in Rat 9L gliosarcomas but have reduced cytolytic function.

    abstract::To better understand immune responses to brain tumors and to develop possible approaches for immunotherapy, we have investigated the leukocyte populations infiltrating the rat 9L gliosarcoma. By immunocytochem-ical analyses of the cells infiltrating the tumor, we observed a substantial number of cells expressing natur...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Chambers WH,Bozik ME,Brissette-Storkus SC,Basse P,Redgate E,Watkins S,Boggs SS

    更新日期:1996-08-01 00:00:00

  • Cell division is required for de novo methylation of CpG islands in bladder cancer cells.

    abstract::Cell division is essential for tumor development and progression. Methylation-mediated silencing caused by aberrant de novo methylation of CpG islands located in the promoter regions of growth regulatory genes occurs frequently in human cancers. We investigated the relationship between cell division and de novo methyl...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Velicescu M,Weisenberger DJ,Gonzales FA,Tsai YC,Nguyen CT,Jones PA

    更新日期:2002-04-15 00:00:00

  • Integrin alpha1beta1 and alpha2beta1 are the key regulators of hepatocarcinoma cell invasion across the fibrotic matrix microenvironment.

    abstract::As with many types of cancer, cell motility is an important factor in the progression and metastasis of hepatocellular carcinomas (HCC). HCC is associated with significant fibrosis in the liver. The fibrotic microenvironment in the liver is characterized by an altered composition of the extracellular matrix (ECM) and ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Yang C,Zeisberg M,Lively JC,Nyberg P,Afdhal N,Kalluri R

    更新日期:2003-12-01 00:00:00

  • High DNA methyltransferase 3B expression mediates 5-aza-deoxycytidine hypersensitivity in testicular germ cell tumors.

    abstract::Testicular germ cell tumors (TGCT) are the most common solid tumors of 15- to 35-year-old men. TGCT patients are frequently cured with cytotoxic cisplatin-based therapy. However, TGCT patients refractory to cisplatin-based chemotherapy have a poor prognosis, as do those having a late relapse. Pluripotent embryonal car...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-09-1490

    authors: Beyrouthy MJ,Garner KM,Hever MP,Freemantle SJ,Eastman A,Dmitrovsky E,Spinella MJ

    更新日期:2009-12-15 00:00:00

  • Inhibition of ATM Increases Interferon Signaling and Sensitizes Pancreatic Cancer to Immune Checkpoint Blockade Therapy.

    abstract::Combinatorial strategies are needed to overcome the resistance of pancreatic cancer to immune checkpoint blockade (ICB). DNA damage activates the innate immune response and improves ICB efficacy. Because ATM is an apical kinase in the radiation-induced DNA damage response, we investigated the effects of ATM inhibition...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-19-0761

    authors: Zhang Q,Green MD,Lang X,Lazarus J,Parsels JD,Wei S,Parsels LA,Shi J,Ramnath N,Wahl DR,Pasca di Magliano M,Frankel TL,Kryczek I,Lei YL,Lawrence TS,Zou W,Morgan MA

    更新日期:2019-08-01 00:00:00

  • Human monocytes, but not dendritic cells derived from them, are defective in base excision repair and hypersensitive to methylating agents.

    abstract::Monocytes and dendritic cells are key players in the immune response. Because dendritic cells drive the tumor host defense, it is important that monocytes and dendritic cells survive cytotoxic tumor therapy. Although most of the anticancer drugs target DNA, the DNA repair capacity of monocytes and dendritic cells has ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-06-3712

    authors: Briegert M,Kaina B

    更新日期:2007-01-01 00:00:00

  • Comparative structure-genotoxicity study of three aminoanthraquinone drugs and doxorubicin.

    abstract::Two aminoanthraquinone analogs 1,4-bis(2-[(2-hydroxyethyl)amino]ethylamino)-9,10-anthracenedione (HAQ) and 1,4-dihydroxy-5,8-bis(2-[(2-hydroxyethyl)amino]ethylamino]-9,10-anthracenedione (DHAQ) have been shown to possess similar therapeutic activities against experimental tumors but different toxicities to the animal...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Au WW,Butler MA,Matney TS,Loo TL

    更新日期:1981-02-01 00:00:00

  • Enhancement of antitumor transplantation resistance in rats by appropriately timed administration of busulfan.

    abstract::Enhancement of specific transplantation resistance to a syngeneic tumor (KMT-17) was observed in WKA rats by treatment with the antileukemia drug busulfan (BU) (15 mg/kg) 5 days before and 5 days after immunization with X-irradiated KMT-17 tumor cells. Rats immunized with X-irradiated KMT-17 cells and then treated wit...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Mizushima Y,Sendo F,Takeichi N,Hosohawa M,Kobayashi H

    更新日期:1981-07-01 00:00:00

  • High levels of dioxin-like potential in cigarette smoke evidenced by in vitro and in vivo biosensing.

    abstract::Cigarette smoke contains low levels of agonists for the aryl hydrocarbon receptor (AhR; also called the dioxin receptor). However, little is understood about the whole potential of cigarette smoke for activating AhR. In this report, we evaluated the total "dioxin-like" activity of cigarette smoke using in vitro and in...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-05-4541

    authors: Kasai A,Hiramatsu N,Hayakawa K,Yao J,Maeda S,Kitamura M

    更新日期:2006-07-15 00:00:00

  • Development of a highly active nanoliposomal irinotecan using a novel intraliposomal stabilization strategy.

    abstract::Liposome formulations of camptothecins have been actively pursued because of the potential for significant pharmacologic advantages from successful drug delivery of this important class of anticancer drugs. We describe nanoliposomal CPT-11, a novel nanoparticle/liposome construct containing CPT-11 (irinotecan) with un...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-05-4007

    authors: Drummond DC,Noble CO,Guo Z,Hong K,Park JW,Kirpotin DB

    更新日期:2006-03-15 00:00:00

  • Luteolin inhibits vascular endothelial growth factor-induced angiogenesis; inhibition of endothelial cell survival and proliferation by targeting phosphatidylinositol 3'-kinase activity.

    abstract::In an attempt to identify phytochemicals contributing to the well-documented preventive effect of plant-based diets on cancer incidence and mortality, we have previously shown that certain flavonoids inhibit in vitro angiogenesis. Here, we show that the flavonoid luteolin inhibited tumor growth and angiogenesis in a m...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-03-3104

    authors: Bagli E,Stefaniotou M,Morbidelli L,Ziche M,Psillas K,Murphy C,Fotsis T

    更新日期:2004-11-01 00:00:00

  • Ovarian carcinoma expresses the NKG2D ligand Letal and promotes the survival and expansion of CD28- antitumor T cells.

    abstract::The role of the NKG2D immunoreceptor and its ligands in antitumor immune response is incompletely understood. Here, we report that effector immune cells infiltrating ovarian carcinoma are mostly CD8+ lymphocytes lacking CD28 but expressing the NKG2D costimulatory receptor. Human ovarian carcinoma expresses the novel N...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.can-03-2194

    authors: Conejo-Garcia JR,Benencia F,Courreges MC,Gimotty PA,Khang E,Buckanovich RJ,Frauwirth KA,Zhang L,Katsaros D,Thompson CB,Levine B,Coukos G

    更新日期:2004-03-15 00:00:00

  • 2-Amino-6-methoxypurine arabinoside: an agent for T-cell malignancies.

    abstract::Earlier studies have shown guanine arabinoside (ara-G) is an effective agent against growth of T-cell lines and freshly isolated human T-leukemic cells. However, poor water solubility of ara-G limits clinical use. 2-Amino-6-methoxypurine arabinoside (506U) is a water-soluble prodrug converted to ara-G by adenosine dea...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Lambe CU,Averett DR,Paff MT,Reardon JE,Wilson JG,Krenitsky TA

    更新日期:1995-08-01 00:00:00

  • Effect of dietary 2(3)-tert-butyl-4-hydroxyanisole on the metabolism and action of estradiol and estrone in female CD-1 mice.

    abstract::Administration of 0.75% 2(3)-tert-butyl-4-hydroxyanisole (BHA) in AIN-76A diet to female CD-1 mice for 3 weeks increased liver microsomal glucuronidation of estradiol, estrone, 4-aminophenol, and 4-nitrophenol by 103, 187, 162, and 92%, respectively (at pH 7.4). The overall rate of NADPH-dependent metabolism of estrad...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Zhu BT,Lech J,Rosen RT,Conney AH

    更新日期:1997-06-15 00:00:00

  • Influence of 1-beta-D-arabinofuranosylcytosine conjugates of lipids on the growth and metastasis of Lewis lung carcinoma.

    abstract::Five different lipid conjugates of 1-beta-D-arabinofuranosylcytosine (ara-C) were tested for their therapeutic activity on the growth and metastasis of Lewis lung carcinoma (3-LL). Among 1 ester-linked lipid conjugate (Ara-CDP-L-dipalmitin), 3 1-O-alkyl-lipid conjugates (ara-CDP-D,L-PBA, ara-CDP-D,L-PCA, ara-CDP-D,L-M...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Berdel WE,Danhauser S,Hong CI,Schick HD,Reichert A,Busch R,Rastetter J,Vogler WR

    更新日期:1988-02-15 00:00:00

  • Regional heterogeneity and complementation in the expression of the tumor-associated glycoprotein 72 epitopes in colorectal cancer.

    abstract::We analyzed the immunohistochemical expression of three epitopes of the tumor-associated glycoprotein 72 (TAG-72) in whole cross-sections of primary colorectal carcinomas and in regional lymph node metastases using monoclonal antibodies (MAbs) B72.3, CC-49, and CC-83, which recognize distinct carbohydrate antigenic de...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Muraro R,Frati L,Bei R,Ficari F,Valli C,French D,Mammarella S,Caramia F,Fegiz G,Mariani-Costantini R

    更新日期:1991-10-01 00:00:00

  • ZMYND8 expression in breast cancer cells blocks T-lymphocyte surveillance to promote tumor growth.

    abstract::Emerging studies indicate that DNA damage in cancer cells triggers antitumor immunity, but its intrinsic regulatory mechanism in breast cancer cells remains poorly understood. Here, we show that ZMYND8 is upregulated and inhibits micronucleus formation and DNA damage in breast cancer cells. Loss of ZMYND8 triggered ac...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-20-1710

    authors: Wang Y,Luo M,Chen Y,Wang Y,Zhang B,Ren Z,Bao L,Wang Y,Wang JE,Fu YX,Luo W,Wang Y

    更新日期:2020-11-04 00:00:00

  • In vivo administration of MKT-077 causes partial yet reversible impairment of mitochondrial function.

    abstract::The effects of in vivo administration of a pharmacologically toxic dose of the lipophilic cationic compound, MKT-077, were investigated in selected vital organs of the rat. MKT-077 (15 mg/kg body weight), administered by bolus i.v. injection every day for 5 days, did not detectably influence rat heart and kidney mitoc...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Weisberg EL,Koya K,Modica-Napolitano J,Li Y,Chen LB

    更新日期:1996-02-01 00:00:00

  • A selective effect of methylglyoxal-bis(guanylhydrazone) on the synthesis of mitochondrial DNA of cultured L1210 leukemia cells.

    abstract::Methylglyoxal-bis(guanylhydrazone) (MGBG) is a polycationic drug which is useful in the chemotherapy of lymphoid and myeloid proliferative disorders. The drug has recently been shown to produce selective ultrastructural damage to the mitochondria of proliferating cell populations. It is important to understand the mol...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Feuerstein B,Porter CW,Dave C

    更新日期:1979-10-01 00:00:00

  • Effects of the immunosuppressive drug niridazole in isogeneic and allogeneic mouse tumor systems in vivo.

    abstract::In both isogeneic (Sarcoma 1 in A/JAX mice) and allogeneic (Sarcoma 180 in C57BL/6 mice) mouse tumor systems, treatment of the tumor-bearing mice with niridazole, an antiprarasitic drug, known to be a potent suppressor of cell mediated but not humoral immunity caused enhancement of metastases to regional popliteal nod...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Deodhar SD,Lee VW,Chiang T,Mahmoud AF,Watten KS

    更新日期:1976-09-01 00:00:00

  • Antiproliferative effects of enediynes on AIDS-derived Kaposi's sarcoma cells.

    abstract::We have investigated the antiproliferative and cytotoxic effects of selected enediynes against three Kaposi's sarcoma (KS) cell lines. The enediynes tested were found to be very potent in inhibiting the growth of KS cells. Treatment with concentrations of 10(-10) M or less were capable of producing 50% inhibition of g...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Corbeil J,Richman DD,Wrasidlo W,Nicolaou KC,Looney DJ

    更新日期:1994-08-15 00:00:00

  • Sustained small interfering RNA delivery by mesoporous silicon particles.

    abstract::RNA interference (RNAi) is a powerful approach for silencing genes associated with a variety of pathologic conditions; however, in vivo RNAi delivery has remained a major challenge due to lack of safe, efficient, and sustained systemic delivery. Here, we report on a novel approach to overcome these limitations using a...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:10.1158/0008-5472.CAN-09-3931

    authors: Tanaka T,Mangala LS,Vivas-Mejia PE,Nieves-Alicea R,Mann AP,Mora E,Han HD,Shahzad MM,Liu X,Bhavane R,Gu J,Fakhoury JR,Chiappini C,Lu C,Matsuo K,Godin B,Stone RL,Nick AM,Lopez-Berestein G,Sood AK,Ferrari M

    更新日期:2010-05-01 00:00:00

  • Von Hippel-Lindau tumor suppressor protein transforms human neuroblastoma cells into functional neuron-like cells.

    abstract::Von Hippel-Lindau (VHL) tumor suppressor protein is expressed in neurons of the central nervous system and plays an important role during the neuronal differentiation of central nervous system progenitor cells. To elucidate the neuronal differentiating potential of VHL protein in neuroblastoma cells, we overexpressed ...

    journal_title:Cancer research

    pub_type: 杂志文章

    doi:

    authors: Murata H,Tajima N,Nagashima Y,Yao M,Baba M,Goto M,Kawamoto S,Yamamoto I,Okuda K,Kanno H

    更新日期:2002-12-01 00:00:00