Abstract
Biosurfactants are natural compounds produced biologically by certain bacterial strains. They are promising alternatives in several applications due to their biocompatibility, biodegradability and reduced toxicity. Systemic toxicity problems and drug resistance in tumor chemotherapy are urging the continued discovery of new antitumor agents. Biosurfactants have significant effect in inhibiting multiple tumor types. Specifically, surfactin, iturin, and fengycin lipopeptide biosurfactant were previously produced from several bacterial species belonging to Bacillus genus. Only few previous studies investigated their cytotoxicity against some tumor types such as breast, colon, leukemia, hepatoma and others. Due to the probability of being potential antitumor treatments, biosurfactants nanoparticles could be clinically recommended. This review discussed the properties of biologically-produced biosurfactants and their antitumor activities against distinctive cancer models. Additionally, it underlines their potential mechanisms and sheds light on the discovery of new active bioproducts.
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Abbreviations
- ERK:
-
Extracellular sign controlled kinase
- ERS:
-
Endoplasmic reticulum stress
- DOX:
-
Doxorubicin
- IC50 :
-
Half inhibition concentration
- Bcl-xL:
-
B-cell lymphoma-extra large
- MDR:
-
Multidrug Resistant
- HMEC:
-
Human mammary epithelial cells
- TPA:
-
Tetradecanoylphorbol-13-acetic acid
- ROS/JNK:
-
Reactive oxygen species/c-Jun N-terminal kinase
- Akt:
-
Protein Kinase B pathway
- MMP-9:
-
Matrix metallopeptidase-9
- MPTP:
-
Mitochondrial penetrability change pore
- ROS:
-
Reactive oxygen species
- BH3:
-
BCL-2 homology
- CLPs:
-
Crude cyclic lipopeptides
- Cyto-C:
-
Cytochrome-C
- Bcl-2:
-
B-cell lymphoma 2
- PS:
-
Phosphatidylserine
- MOMP:
-
Mitochondrial outer membrane permeabilization
- Apaf-1:
-
Apoptotic protease activating factor-1
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Rofeal, M., El-Malek, F.A. Valorization of Lipopeptides Biosurfactants as Anticancer Agents. Int J Pept Res Ther 27, 447–455 (2021). https://doi.org/10.1007/s10989-020-10105-8
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DOI: https://doi.org/10.1007/s10989-020-10105-8