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. 2023 Jul 18;16(7):1021. doi: 10.3390/ph16071021

Table 4.

Induction of differentiation by green tea catechins.

Model Compound/Component Effect Reference
In vitro
HL60 NB4 EGCG
0–40 µmol/L (24–36h) ATRA—1 µmol/L
Induction of neutrophil differentiation—↑ CD11b surface expression
EGCG + ATRA—↑ CD11b and CD15 expression; ↑ CEBPE, CSF3R and DAPK2; and ↓ of undifferentiated promyelocytes and myelocytes
[16]
NB4 NB4 R1
NB4 R2
Catechins
100–200 µM (12–24 h)
Induction of PML/RARα degradation [33]
NB4 EGCG
0–30 µM (72 h)
ATRA—10 µM
Induction of PML-RARα degradation by inhibition of Pin1 (↓) [107]
HL-60 NB4 EGCG
0–100 µM (24–72 h)
ATRA—10 µM
Induction of granulocytic maturation—morphological changes and ↑ NBT reduction ability; and degradation of PML/RARα (↓) and HDAC1 (↓) [106]
HL60 NB4 THP-1 EGCG
5–40 µM (48 h)
ATRA 1 µM/mL
Induction of PML/RARα degradation (↓) and restored PML (↑) and PTEN (↑) function
EGCG + ATRA—↑ PTEN, CD11b, CEBPE
[108]
NB4 EGCG
12.5–20 µg/mL
ATRA—1 µM
Induction of neutrophil differentiation—↑ of CD11b, CD14, CD15 and CD66 surface expression
EGCG + ATRA—↑ CD15 expression
[7]
In vivo—Xenograft and systemics model
CTSG-PML-RARA
transgenic mice cells in C57BL/6J mice
EGCG
12.50 mg/kg/d
intraperitoneally for 21 days
ATRA—5 mg
Induction of PML-RARα degradation in bone marrow cells and ↓ of spleen weight [107]
hCG-PML/RAR
transgenic mice cells in NOD. CB17-Prkdcscid/J mice
EGCG
25 mg/kg/d intraperitoneally, for 5 days
Induction of differentiation—↓ immature cells and undifferentiated promyelocytes in the bone marrow, ↑ mature myeloid cells, ↓ PIN1 and its substrates—cyclin D, NFκB, c-Myc and AKT and ↑ ROS; ↓ of spleen weight [7]