The cell-line-derived subcutaneous tumor model in preclinical cancer research

SM Stribbling, AJ Ryan - Nature Protocols, 2022 - nature.com
Tumor-bearing experimental animals are essential for preclinical cancer drug development.
A broad range of tumor models is available, with the simplest and most widely used …

Single-agent and combination therapeutic strategies to inhibit hepatocyte growth factor/MET signaling in cancer

L Toschi, PA Janne - Clinical Cancer Research, 2008 - AACR
Receptor tyrosine kinases are often aberrantly activated in human malignancies and
contribute to cancer development and progression. Specific receptor tyrosine kinase …

Vasohibin-1 expression in endothelium of tumor blood vessels regulates angiogenesis

T Hosaka, H Kimura, T Heishi, Y Suzuki… - The American journal of …, 2009 - Elsevier
In this study, we characterized the significance of the vascular endothelial growth factor-
inducible angiogenesis inhibitor vasohibin-1 to tumors. In pathological sections of non-small …

Metformin enhances the radiosensitizing effect of cisplatin in non-small cell lung cancer cell lines with different cisplatin sensitivities

MA Riaz, A Sak, YB Erol, M Groneberg, J Thomale… - Scientific reports, 2019 - nature.com
Cisplatin is an extensively used chemotherapeutic drug for lung cancer, but the
development of resistance decreases its effectiveness in the treatments of non-small cell …

The shadow of death on the MET tyrosine kinase receptor

D Tulasne, B Foveau - Cell Death & Differentiation, 2008 - nature.com
The MET tyrosine kinase receptor is a high-affinity receptor for hepatocyte growth
factor/scatter factor (HGF/SF). HGF/SF-MET system is necessary for embryonic development …

HSP27 is required for invasion and metastasis triggered by hepatocyte growth factor

S Pavan, D Musiani, E Torchiaro… - … journal of cancer, 2014 - Wiley Online Library
The hepatocyte growth factor (HGF) also known as scatter factor activates cancer cell
invasion and metastasis. We show that in ovarian cancer cells HGF induced the …

Novel targeting of phospho-cMET overcomes drug resistance and induces antitumor activity in multiple myeloma

M Moschetta, A Basile, A Ferrucci, MA Frassanito… - Clinical cancer …, 2013 - AACR
Purpose: The aim of the study was to verify the hypothesis that the cMet oncogene is
implicated in chemio-and novel drug resistance in multiple myeloma. Experimental Design …

Heat‐shock protein 27 (HSP 27, HSPB 1) is synthetic lethal to cells with oncogenic activation of MET, EGFR and BRAF

JD Konda, M Olivero, D Musiani, S Lamba… - Molecular …, 2017 - Wiley Online Library
The small heat‐shock protein of 27 kDa (HSP 27) is highly expressed in many cancers and
is associated with aggressive tumour behaviour, metastasis, poor prognosis and resistance …

Significance of c‐MET overexpression in cytotoxic anticancer drug‐resistant small‐cell lung cancer cells

H Ozasa, T Oguri, K Maeno, O Takakuwa… - Cancer …, 2014 - Wiley Online Library
The c‐MET receptor tyrosine kinase is the receptor for hepatocyte growth factor. Recently,
activation of the c‐MET/hepatocyte growth factor signaling pathway was associated with …

[HTML][HTML] HGF/c-Met axis drives cancer aggressiveness in the neo-adjuvant setting of ovarian cancer

M Mariani, M McHugh, M Petrillo, S Sieber, S He… - Oncotarget, 2014 - ncbi.nlm.nih.gov
Ovarian cancer is the most lethal gynecologic malignancy. Recently, NACT (Neo Adjuvant
Chemotherapy) has been tested as alternative approach for the management of ovarian …