Review
Ivermectin, a potential anticancer drug derived from an antiparasitic drug

https://doi.org/10.1016/j.phrs.2020.105207Get rights and content

Highlights

  • Ivermectin effectively suppresses the proliferation and metastasis of cancer cells and promotes cancer cell death at doses that are nontoxic to normal cells.

  • Ivermectin shows excellent efficacy against conventional chemotherapy drug-resistant cancer cells and reverses multidrug resistance.

  • Ivermectin combined with other chemotherapy drugs or targeted drugs has powerful effects on cancer.

  • The structure of crosstalk centered on PAK1 kinase reveals the mechanism by which ivermectin regulates multiple signaling pathways.

  • Ivermectin has been used to treat parasitic diseases in humans for many years and can quickly enter clinical trials for the treatment of tumors.

Abstract

Ivermectin is a macrolide antiparasitic drug with a 16-membered ring that is widely used for the treatment of many parasitic diseases such as river blindness, elephantiasis and scabies. Satoshi ōmura and William C. Campbell won the 2015 Nobel Prize in Physiology or Medicine for the discovery of the excellent efficacy of ivermectin against parasitic diseases. Recently, ivermectin has been reported to inhibit the proliferation of several tumor cells by regulating multiple signaling pathways. This suggests that ivermectin may be an anticancer drug with great potential. Here, we reviewed the related mechanisms by which ivermectin inhibited the development of different cancers and promoted programmed cell death and discussed the prospects for the clinical application of ivermectin as an anticancer drug for neoplasm therapy.

Graphical abstract

Ivermectin has powerful antitumor effects, including the inhibition of proliferation, metastasis, and angiogenic activity, in a variety of cancer cells. This may be related to the regulation of multiple signaling pathways by ivermectin through PAK1 kinase. On the other hand, ivermectin promotes programmed cancer cell death, including apoptosis, autophagy and pyroptosis. Ivermectin induces apoptosis and autophagy is mutually regulated. Interestingly, ivermectin can also inhibit tumor stem cells and reverse multidrug resistance and exerts the optimal effect when used in combination with other chemotherapy drugs.

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Abbreviations

ASC
Apoptosis-associated speck-like protein containing a CARD
ALCAR
acetyl-L-carnitine
CSCs
Cancer stem cells
DAMP
Damage-associated molecular pattern
EGFR
Epidermal growth factor receptor
EBV
Epstein-Barr virus
EMT
Epithelial mesenchymal-transition
GABA
Gamma-aminobutyric acid
GSDMD
Gasdermin D
HBV
Hepatitis B virus
HCV
Hepatitis C virus
HER2
Human epidermal growth factor receptor 2
HMGB1
High mobility group box-1 protein
HSP27
Heat shock protein 27
LD50
median lethal dose
LDH
Lactate dehydrogenase
IVM
Ivermectin
MDR
Multidrug resistance
NAC
N-acetyl-L-cysteine
OCT-4
Octamer-binding protein 4
PAK1
P-21-activated kinases 1
PAMP
Pathogen-associated molecular pattern
PARP
poly (ADP- ribose) polymerase
P-gp
P-glycoprotein
PRR
pattern recognition receptor
ROS
Reactive oxygen species
STAT3
Signal transducer and activator of transcription 3
SID
SIN3-interaction domain
siRNA
small interfering RNA
SOX-2
SRY-box 2
TNBC
Triple-negative breast cancer
YAP1
Yes-associated protein 1

Chemical compounds reviewed in this article

ivermectin(PubChem CID:6321424)
avermectin(PubChem CID:6434889)
selamectin(PubChem CID:9578507)
doramectin(PubChem CID:9832750)
moxidectin(PubChem CID:9832912)

Keywords

ivermectin
cancer
drug repositioning

Cited by (0)

1

These authors contributed equally.

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