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Updated: Jun 15, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Plant ribonucleases and nucleases as antiproliferative agens targeting human tumors growing in mice
Jaroslav Matousek1, Josef Matousek
1Biology Centre, Academy of Sciences of the Czech Republic v.v.i., Institute of Plant Molecular Biology, Ceské Budejovice. matousek@iapg.cas.cz
Abstract:
The antiproliferative and antitumor effect of leaf ribonuclease was tested in vitro on the human ML-2 tumor cell line and in vivo on athymic nude mice bearing human melanoma tumors. The antiproliferative activity of this plant ribonuclease in vitro studies was negligible. In the experiments in vivo a significant decrease of the tumor size, however was observed. From nucleases the mung bean nuclease (PhA) was studied first from nucleases. The antitumor effect of this enzyme on ML2 human tumor cell line was almost non-effective. However, significant antitumor activity was detected on human melanoma tumors in vivo. The antitumor effect of black pine pollen nuclease (PN) tested in vitro was also negligible. On the other side, in the experiments in vivo a significant decrease of the human melanoma tumor size was observed too. Recombinant plant nucleases of tomato (TBN1) and hop (HBN1) (submitted to patenting under no. PV 2008-384;Z7585) were isolated to homogeneity and examined for their antitumor effects and cytotoxicity. Although antiproliferative effects of both recombinant nucleases were not significant on the ML-2 cell culture in vitro, the nucleases were strongly cytostatic in vivo after their administration intravenously as stabilized conjugates with polyethylene glycol (PEG). Recombinant both nucleases were as effective against human melanoma tumors as previously studied pine pollen (PN) and mung bean nucleases and their effects were reached at about ten times lower concentrations compared to the use of bovine seminal RNase (BS-RNase).
Insights
Plant nucleases show negligible antiproliferative effects in vitro but significant antitumor activity in vivo against melanoma. Recombinant nucleases, like TBN1 and HBN1, demonstrate potent cytostatic effects in vivo, offering a promising cancer therapy approach.
Area of Science:
- Biochemistry
- Oncology
- Enzymology
Background:
- Plant-derived ribonucleases (RNases) are being investigated for potential therapeutic applications.
- Previous studies have shown varying efficacy of different nucleases against cancer cell lines and tumors.
Purpose of the Study:
- To evaluate the in vitro and in vivo antitumor and antiproliferative effects of various plant nucleases.
- To assess the efficacy of recombinant tomato (TBN1) and hop (HBN1) nucleases against human melanoma tumors.
Main Methods:
- In vitro testing on human ML-2 tumor cell line.
- In vivo studies on athymic nude mice bearing human melanoma tumors.
- Administration of nucleases as stabilized conjugates with polyethylene glycol (PEG).
Main Results:
- Plant nucleases exhibited negligible in vitro antiproliferative activity but significant in vivo antitumor effects on melanoma.
- Recombinant TBN1 and HBN1 nucleases showed strong in vivo cytostatic effects.
- Recombinant nucleases were effective at concentrations ten times lower than bovine seminal RNase (BS-RNase).
Conclusions:
- Plant nucleases, particularly recombinant TBN1 and HBN1, possess significant in vivo antitumor potential against melanoma.
- PEG-stabilized recombinant nucleases offer a promising strategy for cancer therapy due to their potent in vivo activity and reduced dosage requirements.
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