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The effects of patchouli alcohol and combination with cisplatin on proliferation, apoptosis and migration in B16F10 melanoma cells.

Journal of cellular and molecular medicine
May 1, 2023
Kai-Fu Chang et al. (8 authors)
Journal ArticleResearch Support, Non-U.S. Gov'tMolecular Study
Extracted Claims (13)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Patchouli alcohol (PA)
decrease
proliferation of B16F10 cells
B16F10 cells
dose- and time-dependent manner
selectively inhibited
#1
Patchouli alcohol (PA)
increase
cell cycle arrest at the G0/G1 phase
B16F10 cells
-
induced
#2
Patchouli alcohol (PA)
increase
typical morphological changes in apoptosis
B16F10 cells
-
induced
#3
Patchouli alcohol (PA)
decrease
migratory ability of B16F10 cells
B16F10 cells
-
reduced
#4
Patchouli alcohol (PA)
increase
E-cadherin expression
B16F10 cells
-
upregulating
#5
Patchouli alcohol (PA)
decrease
p-Smad2/3 expression
B16F10 cells
-
downregulating
#6
Patchouli alcohol (PA)
decrease
vimentin expression
B16F10 cells
-
downregulating
#7
Patchouli alcohol (PA)
decrease
MMP-2 expression
B16F10 cells
-
downregulating
#8
Patchouli alcohol (PA)
decrease
MMP-9 expression
B16F10 cells
-
downregulating
#9
Patchouli alcohol (PA)
decrease
tumour growth
in vivo
-
strongly suppressed
#10
PA combined with cisplatin
decrease
colony formation of B16F10 cells
B16F10 cells
-
synergistically inhibited
#11
PA combined with cisplatin
decrease
migration of B16F10 cells
B16F10 cells
-
synergistically inhibited
#12
PA combined with cisplatin
decrease
development of resistance to treatment
B16F10 cells
-
attenuated
#13
Abstract

Melanoma is a highly metastatic cancer with a low incidence rate, but a high mortality rate. Patchouli alcohol (PA), a tricyclic sesquiterpene, is considered the main active component in Pogostemon cablin Benth, which improves wound healing and has anti-tumorigenic activity. However, the pharmacological action of PA on anti-melanoma remains unclear. Thus, the present study aimed to investigate the role of PA in the proliferation, cell cycle, apoptosis and migration of melanoma cells. These results indicated that PA selectively inhibited the proliferation of B16F10 cells in a dose- and time-dependent manner. It induced cell cycle arrest at the G0 /G1 phase and typical morphological changes in apoptosis, such as chromatin condensation, DNA fragmentation and apoptotic bodies. In addition, PA reduced the migratory ability of B16F10 cells by upregulating E-cadherin and downregulating p-Smad2/3, vimentin, MMP-2 and MMP-9 expression. PA was also found to strongly suppress tumour growth in vivo. Furthermore, PA combined with cisplatin synergistically inhibited colony formation and migration of B16F10 cells and attenuated the development of resistance to treatment. Therefore, the results of this study indicate that PA may play a pivotal role in inducing apoptosis and reducing the migration of melanoma cells, and may thus be a potential candidate for melanoma treatment.

Medical Subject Headings (MeSH)
HumansCisplatinSesquiterpenesMelanomaCell Line, TumorApoptosisCell Proliferation
Study Links
Citation Metrics
Total Citations7
Citations/Year3.5
Relative Citation Ratio1.48
NIH Percentile64.6%
Research Impact Scores
APT Score0.05
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