» Articles » PMID: 27491866

Interaction of a Standardized Mistletoe (Viscum Album) Preparation with Antitumor Effects of Trastuzumab in Vitro

Overview
Publisher Biomed Central
Date 2016 Aug 6
PMID 27491866
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Besides conventional anticancer therapy many breast cancer patients use complementary and alternative medicine (CAM) like the medicinal herb mistletoe (Viscum album L.). To gain more knowledge about possible herb-drug interactions between CAM and conventional anticancer medications, in the present in vitro study we investigated the effect of a standardized mistletoe preparation on the action of Trastuzumab, a drug used for the treatment of Her-2 positive breast cancer.

Methods: The Her-2 positive human breast carcinoma cell line SK-BR-3 was treated with Trastuzumab. Different doses of the drug were combined with Viscum album extract (VAE) in clinically relevant doses. Proliferation, apoptosis, cell cycle and the secretion of vascular endothelial growth factor (VEGF) were analyzed.

Results: No inhibition of antitumor efficacy of Trastuzumab by VAE was detected. VAE and Trastuzumab, either alone or in combination, inhibited proliferation of SK-BR-3 cells in vitro. At higher concentrations VAE induced apoptosis, which was not observed for Trastuzumab. Cells treated with Trastuzumab underwent a G0/G1 cell cycle arrest and cells treated with VAE a G2/M arrest. After application of the two drugs in combination both G0/G1 and G2/M arrest was observed. VEGF secretion of SK-BR-3 cells was significantly inhibited by sole treatment with Trastuzumab or VAE. Combined treatment of Trastuzumab and VAE at clinically relevant doses showed additive inhibitory effects on VEGF secretion.

Conclusions: VAE did not interfere with cytostatic effects of Trastuzumab on SK-BR-3 cells in vitro. Our in vitro results suggest that no risk of safety by herb drug interactions has to be expected from the exposition of cancer cells to Trastuzumab and VAE simultaneously. In contrast, VAE and Trastuzumab seem to exhibit complementary anti-cancer effects in vitro.

Citing Articles

Mistletoe Extracts from Different Host Trees Disparately Inhibit Bladder Cancer Cell Growth and Proliferation.

Juengel E, Rutz J, Meiborg M, Markowitsch S, Maxeiner S, Grein T Cancers (Basel). 2023; 15(19).

PMID: 37835543 PMC: 10571756. DOI: 10.3390/cancers15194849.


A Novel Mechanism Underlying the Inhibitory Effects of Trastuzumab on the Growth of HER2-Positive Breast Cancer Cells.

Maadi H, Wang Z Cells. 2022; 11(24).

PMID: 36552857 PMC: 9777316. DOI: 10.3390/cells11244093.


Distinct Modulatory Effects of Fever-Range Hyperthermia on the Response of Breast Cancer Cells and Macrophages to Mistletoe ( L.) Extract.

Kozlowski H, Pawlikowska M, Sobocinska J, Jedrzejewski T, Dzialuk A, Wrotek S Pharmaceuticals (Basel). 2021; 14(6).

PMID: 34201348 PMC: 8229697. DOI: 10.3390/ph14060551.


Antibody-drug nanoparticle induces synergistic treatment efficacies in HER2 positive breast cancer cells.

Abedin M, Powers K, Aiardo R, Barua D, Barua S Sci Rep. 2021; 11(1):7347.

PMID: 33795712 PMC: 8016985. DOI: 10.1038/s41598-021-86762-6.


Efficacy of mistletoe extract as a complement to standard treatment in advanced pancreatic cancer: study protocol for a multicentre, parallel group, double-blind, randomised, placebo-controlled clinical trial (MISTRAL).

Wode K, Nordberg J, Kienle G, Elander N, Bernhardson B, Sunde B Trials. 2020; 21(1):783.

PMID: 32917288 PMC: 7488501. DOI: 10.1186/s13063-020-04581-y.


References
1.
Choi Y, Seo H, Choi H, Choi H, Kim S, Shin Y . Induction of Fas-mediated extrinsic apoptosis, p21WAF1-related G2/M cell cycle arrest and ROS generation by costunolide in estrogen receptor-negative breast cancer cells, MDA-MB-231. Mol Cell Biochem. 2011; 363(1-2):119-28. DOI: 10.1007/s11010-011-1164-z. View

2.
Stacey D . Cyclin D1 serves as a cell cycle regulatory switch in actively proliferating cells. Curr Opin Cell Biol. 2003; 15(2):158-63. DOI: 10.1016/s0955-0674(03)00008-5. View

3.
Muthing J, Meisen I, Bulau P, Langer M, Witthohn K, Lentzen H . Mistletoe lectin I is a sialic acid-specific lectin with strict preference to gangliosides and glycoproteins with terminal Neu5Ac alpha 2-6Gal beta 1-4GlcNAc residues. Biochemistry. 2004; 43(11):2996-3007. DOI: 10.1021/bi0301892. View

4.
Molassiotis A, Fernandez-Ortega P, Pud D, Ozden G, Scott J, Panteli V . Use of complementary and alternative medicine in cancer patients: a European survey. Ann Oncol. 2005; 16(4):655-63. DOI: 10.1093/annonc/mdi110. View

5.
Ferlay J, Steliarova-Foucher E, Lortet-Tieulent J, Rosso S, Coebergh J, Comber H . Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012. Eur J Cancer. 2013; 49(6):1374-403. DOI: 10.1016/j.ejca.2012.12.027. View