Review Article

Exploring the Crosstalk between Inflammation and Epithelial-Mesenchymal Transition in Cancer

Table 2

Natural compounds involved in modulation of epithelial-to-mesenchymal transition (EMT).

Natural compoundsMode of action in blocking of EMTReferences

GenisteinSuppress nuclear factor of activated T cells 1 (NFAT1) which induces MET in a hepatocellular carcinoma cell line (HepG2)[98]
Suppress the TGFβ pathway that inhibits endocrine disruptor-induced EMT in ovarian cancer cells (BG-1)[99]
ResveratrolSuppress HIF-1α protein which inhibits hypoxia-induced EMT in osteosarcoma cells[101]
Inhibits the Hh signaling pathway which inhibits LPS-dependent EMT in prostate cancer cell lines (PC-3 and LNCaP)[102]
Induces overexpression of E-cadherin and suppression of vimentin by blocking the TGFβ1/Smads signaling pathway in colorectal cancer cells[103]
Induce MET in pancreatic cancer via suppression of AKT signaling pathways[104]
Suppress the EGF-activated Erk pathway which prevents EGF-activated EMT in the ER-positive breast cancer cell line (MCF-7)[105]
Showed inhibitory action against TGFβ1-induced EMT in lung cancer cells[106]
KaempferolSuppress mesenchymal protein expression in non-small cell lung cancer[107]
Arctigenin (ARC)Prevented TGFβ-induced EMT in lung cancer cells[108]
Baicalin and baicaleinBlock expression of Slug protein and NF-κB signaling pathway that inhibit the TGFβ1-dependent EMT process in mammary epithelial cells[110]
BerberineInduces overexpression of E-cadherin and suppression of N-cadherin, fibronectin, vimentin, Snail, Slug, and zinc finger E-box binding homeobox 1 (Zeb1) protein expression[111]
CelastrolSuppressed the expression of proinflammatory cytokines (IL-1β, IL-6, and TNFα), cyclooxygenase 2 (COX-2), N-cadherin, Vimentin, and Snail. It induces the expression of E-cadherin[112]
Epicatechin-3-gallate (ECG)Induces overexpression of E-cadherin and suppression of mesenchymal proteins which prevent TGFβ1-dependent EMT in lung cancer cells[113]
GeduninDownregulates expression of mesenchymal proteins such as Slug, Snail, N-cadherin, vimentin, and Zeb as well as upregulation of E-cadherin[114]
PlumbaginInduces overexpression of E-cadherin and reduces expression of Snail, Slug, TCF-8/Zeb1, β-catenin, and vimentin which drive reprogramming of the EMT process[115]
CardamoninBlocks the Wnt signaling pathway which prevents EMT in triple-negative breast cancer cells[96]
Luteolin(i) Inhibits the PI3K/AKT/NF-kB/Snail pathway which prevents TGF-1-dependent EMT in lung cancer cells
(ii) Prevents STAT3 signaling which inhibits IL-6-dependent EMT in pancreatic cancer
(iii) Showed anti-EMT activity in paclitaxel-resistant ovarian cancer cells
[96]