Area of research
Oncology · Cell Biology
Research interest
Research interests include Proteoglycans and glycosaminoglycans research, Glycosylation and Glycoproteins Research, Cancer Cells and Metastasis, and Cell Adhesion Molecules Research.
IER2-induced senescence drives melanoma invasion through osteopontin
Functional Characterization of Circulating Tumor Cells (CTCs) from Metastatic ER+/HER2− Breast Cancer Reveals Dependence on HER2 and FOXM1 for Endocrine Therapy Resistance and Tumor Cell Survival: Implications for Treatment of ER+/HER2− Breast Cancer
Cancer microenvironment and genomics: evolution in process
Severe metabolic alterations in liver cancer lead to ERK pathway activation and drug resistance
EGFR/Ras-induced CCL20 production modulates the tumour microenvironment
Id1 and Id3 Are Regulated Through Matrix‐Assisted Autocrine BMP Signaling and Represent Therapeutic Targets in Melanoma
Tspan8 is expressed in breast cancer and regulates E‐cadherin/catenin signalling and metastasis accompanied by increased circulating extracellular vesicles
Loss of ASAP1 in mice impairs adipogenic and osteogenic differentiation of mesenchymal progenitor cells through dysregulation of FAK/Src and AKT signaling
Macrophage-Induced Lymphangiogenesis and Metastasis following Paclitaxel Chemotherapy Is Regulated by VEGFR3
Detection of cellular senescence within human invasive breast carcinomas distinguishes different breast tumor subtypes
‘Normalizing’ the malignant phenotype of luminal breast cancer cells via alpha(v)beta(3)-integrin
A Systematic Approach to Defining the microRNA Landscape in Metastasis
The proteasome inhibitor Bortezomib (Velcade) as potential inhibitor of estrogen receptor-positive breast cancer
Abstract 1443: A systematic approach to the metastatically relevant microRNA landscape
The Disparate Twins: A Comparative Study of CXCR4 and CXCR7 in SDF-1α–Induced Gene Expression, Invasion and Chemosensitivity of Colon Cancer
CD24 Induces Expression of the Oncomir miR-21 via Src, and CD24 and Src Are Both Post-Transcriptionally Downregulated by the Tumor Suppressor miR-34a
Autochthonous Mouse Melanoma and Mammary Tumors do not Express the Pluripotency Genes Oct4 and Nanog
RASSF1A inhibits estrogen receptor alpha expression and estrogen-independent signalling: implications for breast cancer development
Tumor‐initiating properties of breast cancer and melanoma cells <i>in vivo</i> are not invariably reflected by spheroid formation <i>in vitro</i>, but can be increased by long‐term culturing as adherent monolayers
Abstract 143: CD24 induced miR-21 regulation is mainly mediated through Src, and both (CD24, Src) are post-transcriptionally downregulated by miR-34a