Juan Carlos
Montero González
Chercheur depuis 2021
![Foto de Juan Carlos](/img/nophoto.png)
![Foto de Complejo Hospitalario Universitario de Albacete](/img/noimage_org.png)
Complejo Hospitalario Universitario de Albacete
Albacete, EspañaPublications en collaboration avec des chercheurs de Complejo Hospitalario Universitario de Albacete (24)
2021
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MZ1 co-operates with trastuzumab in HER2 positive breast cancer
Journal of Experimental and Clinical Cancer Research, Vol. 40, Núm. 1
2020
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Checkpoint kinase 1 pharmacological inhibition synergizes with dna-damaging agents and overcomes platinum resistance in basal-like breast cancer
International Journal of Molecular Sciences, Vol. 21, Núm. 23, pp. 1-14
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Inhibition of the mitotic kinase PLK1 overcomes therapeutic resistance to BET inhibitors in triple negative breast cancer
Cancer Letters, Vol. 491, pp. 50-59
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Pharmacological screening and transcriptomic functional analyses identify a synergistic interaction between dasatinib and olaparib in triple-negative breast cancer
Journal of Cellular and Molecular Medicine, Vol. 24, Núm. 5, pp. 3117-3127
2019
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Activity of BET-proteolysis targeting chimeric (PROTAC) compounds in triple negative breast cancer
Journal of Experimental and Clinical Cancer Research, Vol. 38, Núm. 1
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Screening and preliminary biochemical and biological studies of [RuCl(p-cymene)(N, N-bis(diphenylphosphino)-isopropylamine)][BF4] in Breast Cancer Models
ACS Omega, Vol. 4, Núm. 8, pp. 13005-13014
2017
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Regulation of the prometastatic neuregulin–MMP13 axis by SRC family kinases: therapeutic implications
Molecular Oncology, Vol. 11, Núm. 12, pp. 1788-1805
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Synthetic lethality interaction between aurora kinases and CHEK1 inhibitors in ovarian cancer
Molecular Cancer Therapeutics, Vol. 16, Núm. 11, pp. 2552-2562
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Targeting basal-like breast tumors with bromodomain and extraterminal domain (BET) and polo-like kinase inhibitors
Oncotarget, Vol. 8, Núm. 12, pp. 19478-19490
2016
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Breast cancer dissemination promoted by a neuregulin-collagenase 3 signalling node
Oncogene, Vol. 35, Núm. 21, pp. 2756-2765
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In silico analysis guides selection of BET Inhibitors for triple-negative breast cancer treatment
Molecular Cancer Therapeutics, Vol. 15, Núm. 8, pp. 1823-1833
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Neuregulin expression in solid tumors: Prognostic value and predictive role to anti-HER3 therapies
Oncotarget, Vol. 7, Núm. 29, pp. 45042-45051
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Targeting the EGF/HER ligand-receptor system in cancer
Current Pharmaceutical Design, Vol. 22, Núm. 39, pp. 5887-5898
2015
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Antitumor activity of the novel multi-kinase inhibitor EC-70124 in triple negative breast cancer
Oncotarget, Vol. 6, Núm. 29, pp. 27923-27937
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Antitumoral activity of the mithralog EC-8042 in triple negative breast cancer linked to cell cycle arrest in G2
Oncotarget, Vol. 6, Núm. 32, pp. 32856-32867
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Phospho-kinase profile of colorectal tumors guides in the selection of multi-kinase inhibitors
Oncotarget, Vol. 6, Núm. 31, pp. 31272-31283
2014
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Active kinase profiling, genetic and pharmacological data define mTOR as an important common target in triple-negative breast cancer
Oncogene, Vol. 33, Núm. 2, pp. 148-156
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Phospho-kinase profile of triple negative breast cancer and androgen receptor signaling
BMC Cancer, Vol. 14, Núm. 1
2012
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Predominance of mTORC1 over mTORC2 in the regulation of proliferation of ovarian cancer cells: Therapeutic implications
Molecular Cancer Therapeutics, Vol. 11, Núm. 6, pp. 1342-1352
2011
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Inhibition of Src family kinases and receptor tyrosine kinases by dasatinib: Possible combinations in solid tumors
Clinical Cancer Research, Vol. 17, Núm. 17, pp. 5546-5552