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Table 2 6-Shogaol in vivo anticancer study (“↑” represents increase/ promotion/activation while “↓” represents inhibition /reduction/inactivation.)

From: Anticancer perspective of 6-shogaol: anticancer properties, mechanism of action, synergism and delivery system

Cancer models

Cancer cell lines

Tumor xenograft sites

Dose/duration and route of administration

Mechanisms

Tumor suppression efficacy

Ref.

Oral cancer

DMBA Induces

Canceration

Male golden Syrian hamsters aged 8–10 weeks

20 mg/kg/day thrice

A week for 16 weeks

Not specified

Inhibit transcriptional

Activate

NF-KB/AP-1

Inhibition

of cell

Proliferation and inflammation

[56]

Non-small cell lung cancer

NCI-H1650

Female BALB/c (nu/nu) mice

10 or 40 mg/kg/day

Three times a week

for 3 weeks

i.p

Ki-67↓ cyclin D1↓

p-AKT↓ STAT3↓

Inhibit

NCI-H1650

lung cancer cell

growth

[49]

A549

Nu/J nude mice on both sides

10 or 30 mg/kg/day

Five times a week

i.p

Induce apoptosis: GSH↑ p53↑ PUMA↑ Bcl-2↓ Bcl-XL↓

Inhibit cell

proliferation

[47]

Prostate cancer

PC-3

the right flanks of athymic nude mice

250 mg/kg

28 days

oral gavage

Anti-tumor proliferation

Inhibition of tumor proliferation

[57]

HMVP2

the flank

of Isogenic FVB/N male mice

50 and 100 mg/kg

every other day

for 32 days

i.p

pSTAT3Y705

cyclin D1↓

survivin↓

The tumor weight was reduced by 48% and 65% at both doses, respectively

[58]

Colon cancer

HCT-116

SW-480

Female athymic nude mice

15 mg/kg/day

The day after

Cancer cell

Injection and

every other day

28 days

i.p

Induce apoptosis:p53↑ bcl-2↓ BAD↑ Caspase3↑ Caspase8↑ Caspase9↑

Induce cell cycle arrest in the G2/M phase:p53↑ p21↑cdc2↓ cdc25A↓

6-Shogaol significantly inhibited the proliferation of HCT-116 cells

[59]

Cervical cancer

HeLa

The right axilla of Female BALB/c

18 nude mice

0,12.5,and,50 mg/kg/day

One time every day

21 Days

Oral gavage

Induce apoptosis:

p-PI3K↓,p-Akt↓

p-mTOR↓

Induce G2/M phase arrest

Inhibition of metastasis

Inhibition of tumor growth in a dose dependent manner

[13]

Leukaemia

CCRF-CEM

Subcutaneous Of female athymic nude mice

80 mg/kg/day

five times a week

60 days

i.p

Induce apoptosis: p53↑ ROS↑ FASN↓

Inhibition of tumour growth

[60]

Liver cancer

SMMC-7721

Inoculated subcutaneously into SCID mice

10 mg/kg or

50 mg/kg/day

28 days

i.p

Induce apoptosis:

ER stress↑

p-eIF2α↓ CHOP↑ caspase↑ PARP↓

The tumor volume of mice in the 6-shogaol administration group was significantly smaller than that of carrier control mice at two treatment doses (10 mg/kg and 50 mg/kg)

[38]

HepG2

Subcutaneously inoculated into the right rib of BALB/c nude mice

50 mg·kg/day

once every 2 days

35 days

Intraperitoneal

injection

Induce apoptosis AKT/mTOR↓ MRP1↓

Induce G0/G1 phase c arrest: AKT/mTOR/MRP1↓

CyclinA2↓ Cyclin D1↓ Cyclin E1↓

Tumor volume was lower in the 6-shogaol group than in the control group

[61]

Pancreatic cancer

PANC-1

the right flank of pathogen-free male BALB/c immunodeficient nude mice

50 mg/kg

once daily

28 days

i.p

Inhibit NF-KB signaling

Effectively inhibits the growth of pancreatic cancer cells

[52]