Table 1. Proposed therapeutic targets of plant-derived extracts and compounds. The targets modulated by each compound are indicated by check mark (√).
Compounds |
Proliferation/ Viability |
Migration/ Invasion |
Apoptosis |
ECM Production |
TGF-β Level |
TGFβR Level |
SMAD Pathway |
AKT Pathway |
ERK Pathway |
Additional Targets |
Literature |
Quercetin |
√ |
|
|
√ |
√ |
√ |
√ |
√ |
√ |
IGF1R |
[14][15][16][17][18] |
Kaempferol |
√ |
|
|
|
|
|
|
|
|
|
[18] |
(–)-Epigallocatechin -3-gallate |
√ |
√ |
|
√ |
|
|
|
√ |
|
STAT3 |
[19][20][21] |
Genistein |
|
|
|
|
|
|
|
|
|
CTGF |
[22] |
Luteolin |
√ |
|
√ |
|
|
|
|
|
|
FRAT1 |
[23] |
Glabridin |
√ |
|
√ |
√ |
|
|
√ |
√ |
|
|
[24] |
Isorhamnetin |
√ |
√ |
|
√ |
|
|
|
√ |
|
S1PR1 |
[25] |
Protocatechuic acid |
√ |
|
|
√ |
|
|
|
|
|
|
[18] |
Gallic acid |
√ |
|
|
√ |
|
|
|
|
|
|
[18] |
p-Coumaric acid |
√ |
|
|
|
|
|
|
|
|
|
[18] |
Ferulic acid |
√ |
|
|
|
|
|
|
|
|
|
[18] |
Chlorogenic acid |
√ |
|
|
√ |
|
|
|
|
|
|
[18] |
Curcumin |
√ |
|
|
√ |
√ |
|
√ |
|
|
|
[18][26] |
Demethoxycurcumin |
|
|
|
√ |
√ |
|
√ |
|
|
|
[26] |
Bisdemethoxycurcumin |
|
|
|
√ |
√ |
|
√ |
|
|
|
[26] |
Resveratrol |
√ |
|
√ |
√ |
√ |
|
√ |
|
|
HSP47, α-SMA |
[27] |
Asiaticoside |
√ |
√ |
|
√ |
|
√ |
√ |
|
√ |
p38, GDF-9 |
[28] |
Asiatic acid |
|
|
|
√ |
|
|
√ |
|
|
PAI-1, PPARγ |
[29][30] |
Ginsenoside Rg3 |
√ |
√ |
|
√ |
|
|
√ |
|
√ |
Angiogenesis |
[31] |
Tagitinin C |
√ |
|
|
√ |
|
|
|
|
|
|
[32] |
Ingenol-mebutate |
√ |
|
√ |
|
|
|
|
|
|
miR-34a |
[33] |
Glycyrrhizin |
√ |
|
√ |
√ |
√ |
|
√ |
√ |
√ |
NF-κB, HMGB1, Autophagy |
[34] |
Oleanolic acid |
√ |
|
|
√ |
|
|
√ |
|
|
MMP1 |
[35] |
Camptothecin |
|
|
|
√ |
|
|
|
|
|
|
[36] |
10,11-Methylenedioxy camptothecin |
√ |
|
|
|
√ |
|
√ |
|
|
PAI-1 |
[37] |
Oxymatrine |
|
|
|
√ |
|
|
√ |
|
|
|
[38] |
Vincristine |
|
|
√ |
|
|
|
|
|
|
|
[39] |
Paclitaxel |
√ |
|
√ |
√ |
√ |
|
|
√ |
|
|
[40] |
Aspidin PB |
|
|
|
√ |
|
|
√ |
√ |
|
CTGF |
[41] |
Tanshinone IIA |
√ |
|
√ |
|
|
|
|
|
|
Survivin |
[42] |
Selenium- polysaccharide |
√ |
|
√ |
|
|
|
|
|
|
PARP |
[43] |
Photodynamic therapy with Hypocrellin A |
√ |
√ |
√ |
√ |
√ |
|
√ |
|
√ |
Autophagy, α-SMA |
[44] |
2. Phenolic Compounds
Quercetin attenuated KF proliferation (IC
50, 25 μg mL
−1) and lowered the expression levels of TGF-β1, TGFβR1/2, collagen 1/3, and fibronectin
[14][15][16][17]. It lowered the expression levels of SMAD2/3/4 and reduced the phosphorylation of SMAD2/3, and the formation of the SMAD2/3/4 complex
[17]. It lowered the expression levels of the insulin-like growth factor 1 receptor (IGF-1R) β subunit, insulin receptor substrate (IRS) 1, PI3K p85 subunit, c-Raf, and reduced the phosphorylation of c-Raf, MEK1/2, ERK1/2, ETS like protein (ELK) 1, and AKT1 in KFs
[15].
(–)-Epigallocatechin-3-gallate (EGCG) attenuated the proliferation, migration, and collagen production of KFs and NFs, and reduced the phosphorylation of STAT3, but not that of SMAD2/3, in KFs
[19]. Green tea extract and EGCG lowered the expression level of collagen 1 and reduced the phosphorylation of AKT, eukaryotic translation initiation factor 4E-binding protein (4E-BP), and p70S6K in KFs stimulated by human leukemic mast cell line HMC-1
[21].
CTGF protein levels were higher in KFs compared to NFs, and genistein reduced the CTGF protein levels in KFs
[22]. Genistein, at different concentrations (37 or 370 μM), had variable effects on the mRNA expression levels of subunit proteins of AP-1, such as c-Jun, c-Fos, and FosB, in skin keratinocytes, NFs, and KFs
[45].
Luteolin decreased the KF viability and the expression levels of cyclin D1, BCL-2, and FRAT1, and increased cell apoptosis, p21, and BAX expression
[23]. The pro-apoptotic effects of luteolin were abolished by overexpressed FRAT1, a GSKβ3 inhibitor causing β-catenin activation in the Wnt signaling pathway, and siRNA-mediated FRAT1 depletion increased cell apoptosis
[23].
Glabridin, a component of
Glycyrrhiza glabra, reduced KF proliferation and collagen production and induced apoptosis by inhibiting the PI3K/AKT and TGF-β1/SMAD signaling pathways in vitro
[24].
Isorhamnetin inhibited the proliferation, migration, invasion, and fibrogenesis of KFs
[25]. It lowered the expression level of S1PR1 and reduced the phosphorylation of PI3K and AKT
[25]. S1PR1 upregulation abolished the inhibitory effects of isorhamnetin on KF proliferation, migration, invasion, and fibrogenesis.
KF proliferation was inhibited by curcumin (2.5 and 5 μg mL
−1), gallic acid (5 and 10 μg mL
−1), quercetin (10 and 20 μg mL
−1), kaempferol (20 μg mL
−1), protocatechuic acid (100 and 200 μg mL
−1), p-coumaric acid (400 μg mL
−1), ferulic acid (400 μg mL
−1), and chlorogenic acid (400 μg mL
−1)
[18].
p-Hydroxy benzoic acid had no effect, and caffeic acid was very toxic
[18]. These effects were attributed to cell cycle arrest rather than apoptosis
[18]. The cell proliferation was resumed after the removal of each phytochemical and relatively slow recovery was seen with quercetin, chlorogenic acid, or curcumin
[18]. Quercetin, gallic acid, protocatechuic acid, and chlorogenic acid more effectively inhibited the collagen lattice contraction by NFs and hypertrophic scar-derived fibroblasts (HSFs) than other compounds
[18]. The collagen lattice contraction resumed when each compound was removed, and the recovery was slowest with quercetin
[18].
Curcuminoids (25–100 nM), consisting of curcumin, demethoxycurcumin, and bisdemethoxycurcumin, lowered the cellular levels of total soluble collagens, pro-collagen 1, fibronectin, and TGF-β1, and reduced the phosphorylation of SMAD2 in KFs stimulated with bleomycin
[26]. Curcumin was the major form of curcuminoids that entered and accumulated inside cells
[26].
Resveratrol attenuated cell proliferation, induced apoptosis, and lowered the expression levels of TGF-β1, collagen 1, α-SMA, and heat shock protein (HSP) 47, which is involved in collagen folding and remodeling
[46][47], in KFs but not in NFs
[27]. It also attenuated cell proliferation, induced apoptosis, and reduced the collagen synthesis of KFs under hypoxia by downregulating hypoxia-inducible factor (HIF)-1α.
3. Terpenoids
Asiaticoside, a component of
Centella asiatica, attenuated KF proliferation and lowered the expression levels of collagen 1/3 and TGFβR1/2
[28]. Asiaticoside did not affect the expression levels or the phosphorylation of SMAD2/3/4 but increased the expression level of SMAD7, which acts as an intracellular antagonist of the TGF-β signaling pathway
[28]. Asiaticoside attenuated KF proliferation, invasion, and the phosphorylation of ERK1/2, p38 MAPK, and SMAD2/3 (linker region) stimulated by GDF-9
[29].
Asiatic acid from
Centella asiatica suppressed the TGF-β1-induced expression of collagen 1 and plasminogen activator inhibitor-1 (PAI-1) and the phosphorylation of SMAD2/3, while increasing SMAD7 expression
[30]. These effects of asiatic acid on KFs were abrogated by PPAR-γ antagonist GW9662 or peroxisome proliferator-activated receptor gamma (PPAR γ) siRNA
[30].
Ginsenoside Rg3 (50 or 100 µg mL
−1) attenuated the proliferation, migration, invasion, angiogenesis, and collagen synthesis of KFs and inhibited the TGF-β/SMAD and ERK-mediated signaling pathways
[31].
Tagitinin C reduced KF viability after 72 h (IC
50, 0.122 μg mL
−1), as potently as mitomycin C (IC
50, 0.120 μg mL
−1)
[32]. Tagitinin C at IC
50 decreased keloid collagen deposition to 53.1% of the control level, whereas mitomycin C IC
50 decreased it to 60.4%
[32]. Tagitinin C and mitomycin C were less toxic to NFs (IC
50; 35.05 μg mL
−1 and 16.21 μg mL
−1, respectively)
[32]. The selective cytotoxicity index of tagitinin C and mitomycin C on KFs versus NFs was calculated to be 287 and 135, respectively
[32].
Treatment of KFs with ingenol-mebutate induced morphological alterations and DNA fragmentation, which were associated with reduced cell growth and increased apoptosis
[33]. It induced the expression of miR-34a in a p53-dependent manner and upregulated proapoptotic genes, such as caspase-10, while downregulating antiapoptotic genes, such as BCL-2
[33].
Glycyrrhizin, a component of
Glycyrrhiza glabra, lowered the expression level of HMGB1 in KFs and attenuated cell proliferation and autophagy while increasing apoptosis
[34]. Glycyrrhizin inhibited the expressions of ERK1/2, AKT, and NF-κB induced by HMGB1
[34]. Glycyrrhizin lowered the expression levels of TGF-β1, SMAD2/3, ERK1/2, collagen 1/3, fibronectin, and elastin in KFs
[34].
Oleanolic acid attenuated the proliferation of KFs
[35]. It lowered the expression levels of intra- and extracellular fibronectin, procollagen 1, and α-SMA while increasing MMP1
[35]. It inhibited the phosphorylation of SMAD2 and SMAD3 and attenuated the increases in fibronectin, procollagen 1, and α-SMA and the decrease in MMP1 in KFs stimulated with TGF-β1.
4. Alkaloids
Camptothecin, originally isolated from
Camptotheca acuminata, is a topoisomerase inhibitor that has been used in cancer therapy
[48]. Camptothecin lowered the expression levels of collagen 1/3 in KFs without causing cellular toxicity
[36]. Its effects on the collagen 3 level were relatively smaller, and consequently, the ratios of collagen 1 to collagen 3 were decreased by the camptothecin treatment
[48].
10,11-Methylenedioxycamptothecin loaded in hyaluronic acid nanoemulsions were delivered percutaneously to the keloid lesion area in a mouse model
[37]. Its internalization by KFs and delivery to the nucleus resulted in decreased cell proliferation
[37]. It increased the expression levels of TGF-β1, SMAD3, and SMAD7, and downregulated PAI-1 in KFs, implicating an overall suppression of the TGF-β-mediated signaling pathway
[37].
Oxymatrine, an alkaloid compound extracted from
Sophora japonica, lowered the expression levels of collagen and SMAD3 in KFs in vitro without affecting the expression levels of TGF-β1, TGFβR1/2, SMAD4, and SMAD7
[38]. Oxymatrine inhibited the phosphorylation and nuclear translocation of SMAD3 induced by TGF-β1
[38]. Thus oxymatrine could attenuate collagen synthesis by inhibiting the TGF-β/SMAD signaling pathway.
Vincristine is one of the vinca alkaloids originally separated from
Catharanthus roseus, and is used as an anticancer drug
[49]. Vincristine inhibited cell proliferation by inducing cell cycle arrest in the G2/M phase and promoting apoptosis in SH-SY5Y human neuroblastoma cells
[50]. Vincristine showed cytotoxicity to the primary KFs and NFs, with higher potency to the latter
[39]. The resistance of KFs could be largely abrogated by verapamil (a calcium channel blocker)
[39].
The treatment of KFs with paclitaxel or LY294002 (a PI3K inhibitor) lowered their expression levels of TNF-α, IL-6, TGF-β1, α-SMA, and collagen 1
[40]. Paclitaxel also blocked the AKT/GSK3β signaling pathway in KFs and keloid tissues
[40]. Paclitaxel-cholesterol-loaded liposomes inhibited KF proliferation, migration, and invasion, and promoted apoptosis and cell cycle arrest in the G
2/M phases more effectively than paclitaxel itself in vitro
[40]. Paclitaxel-cholesterol-loaded liposomes had better performance in inhibiting keloid growth compared to paclitaxel in the keloid-bearing BALB/c nude mouse model
[40].
5. Other Compounds
Aspidin PB inhibited the expression of collagen 1, CTGF, and α-SMA in KFs stimulated by TGF-β1
[41]. It inhibited both the SMAD2/3-mediated signaling pathway and the PI3K/AKT-mediated signaling pathway stimulated by TGF-β1
[41].
Tanshinone IIA attenuated the proliferation of KFs, whereas it did not affect the proliferation of NFs
[42]. It increased the percentages of KF cells in the G
0/G
1 phases and the cells undergoing early apoptosis
[42]. It also decreased the expression of survivin
[42].
A selenium-containing polysaccharide from Ziyang green tea (Se-ZGTP) or short hairpin RNA (shRNA) for neuron-glia 2 inhibited the proliferation of KFs
[43]. Se-ZGTP or NG2 shRNA induced apoptosis mediated by an increase in pro-apoptotic BAX expression, the activation of caspase-3, the subsequent cleavage and inactivation of poly (ADP-ribose) polymerase (PARP), and a decrease in the expression levels of anti-apoptotic BCL-2
[43]. Se-ZGTP or neuron-glia 2 shRNA reduced collagen 1 and protein expression in KFs following TGF-β1 stimulation
[43].
As a photodynamic therapy, the combined treatment of hypocrellin A with a light-emitting diode (LED)’s red light irradiation increased ROS production
[51] and decreased KF viability, proliferation, invasion, collagen production, and the expression of collagen 1/3, α-SMA, and fibronectin, while increasing cell apoptosis and the expression of BAX and caspase-3
[44]. The combined photodynamic therapy reduced autophagy, the protein expression of Beclin-1, and the conversion of LC3-I to LC3-II
[44]. It inhibited the expression of TGF-β and the downstream signaling pathways mediated by ERK1/2 and SMD2/3
[44].