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Selected Publication:
SHR Neuro Cancer Cardio Lipid Metab Microb
Herz, C; Hertrampf, A; Zimmermann, S; Stetter, N; Wagner, M; Kleinhans, C; Erlacher, M; Schüler, J; Platz, S; Rohn, S; Mersch-Sundermann, V; Lamy, E.
The isothiocyanate erucin abrogates telomerase in hepatocellular carcinoma cells in vitro and in an orthotopic xenograft tumour model of HCC.
J Cell Mol Med. 2014; 18(12): 2393-2403.
Doi: 10.1111/jcmm.12412
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- Co-authors Med Uni Graz
- Kleinhans Claudia
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- Abstract:
- In contrast to cancer cells, most normal human cells have no or low telomerase levels which makes it an attractive target for anti-cancer drugs. The small molecule sulforaphane from broccoli is known for its cancer therapeutic potential in vitro and in vivo. In animals and humans it was found to be quickly metabolized into 4-methylthiobutyl isothiocyanate (MTBITC, erucin) which we recently identified as strong selective apoptosis inducer in hepatocellular carcinoma (HCC) cells. Here, we investigated the relevance of telomerase abrogation for cytotoxic efficacy of MTBITC against HCC. The drug was effective against telomerase, independent from TP53 and MTBITC also blocked telomerase in chemoresistant subpopulations. By using an orthotopic human liver cancer xenograft model, we give first evidence that MTBITC at 50 mg/KG b.w./d significantly decreased telomerase activity in vivo without affecting enzyme activity of adjacent normal tissue. Upon drug exposure, telomerase decrease was consistent with a dose-dependent switch to anti-survival, cell arrest and apoptosis in our in vitro HCC models. Blocking telomerase by the specific inhibitor TMPyP4 further sensitized cancer cells to MTBITC-mediated cytotoxicity. Overexpression of hTERT, but not enzyme activity deficient DNhTERT, protected against apoptosis; neither DNA damage nor cytostasis induction by MTBITC was prevented by hTERT overexpression. These findings imply that telomerase enzyme activity does not protect against MTBITC-induced DNA damage but impacts signalling processes upstream of apoptosis execution level. © 2014 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
- Find related publications in this database (using NLM MeSH Indexing)
- Animals -
- Antineoplastic Agents - metabolism
- Antineoplastic Agents - pharmacokinetics
- Antineoplastic Agents - pharmacology
- Apoptosis - drug effects
- Carcinoma, Hepatocellular - drug therapy
- Carcinoma, Hepatocellular - enzymology
- Carcinoma, Hepatocellular - genetics
- Cell Line, Tumor -
- DNA Damage -
- Gene Expression - drug effects
- Hep G2 Cells -
- Humans -
- Immunoblotting -
- Isothiocyanates - metabolism
- Isothiocyanates - pharmacokinetics
- Isothiocyanates - pharmacology
- Kidney - metabolism
- Liver - metabolism
- Liver - pathology
- Liver Neoplasms - drug therapy
- Liver Neoplasms - enzymology
- Liver Neoplasms - genetics
- Mice, Nude -
- Niacinamide - analogs & derivatives
- Niacinamide - pharmacology
- Phenylurea Compounds - pharmacology
- Proto-Oncogene Proteins c-bcl-2 - genetics
- Proto-Oncogene Proteins c-bcl-2 - metabolism
- RNA Interference -
- Reverse Transcriptase Polymerase Chain Reaction -
- Sorafenib -
- Telomerase - antagonists & inhibitors
- Telomerase - metabolism
- Tumor Burden - drug effects
- Tumor Suppressor Protein p53 - genetics
- Tumor Suppressor Protein p53 - metabolism
- Xenograft Model Antitumor Assays -
- Find related publications in this database (Keywords)
- 4-methylthiobutyl isothiocyanate
- erucin
- sulforaphane
- hTERT
- telomerase suppression
- hepatocellular carcinoma and chemoresistant subpopulations
- adjuvant chemotherapy