TY - JOUR
T1 - In vitro pro-apoptotic and anti-migratory effects of Treculia africana Decne. (Moraceae) and Entandrophragma angolense Welw (Meliaceae) extracts on prostate cancer cells
AU - Zingue, Stéphane
AU - Rutz, Jochen
AU - Maxeiner, Sebastian
AU - Ndinteh, Derek Tantoh
AU - Chun, Felix K.H.
AU - Jüngel, Eva
AU - Njamen, Dieudonné
AU - Blaheta, Roman
N1 - Publisher Copyright:
© 2021 Elsevier GmbH
PY - 2021/8
Y1 - 2021/8
N2 - Prostate cancer is the second leading cause of cancer deaths in men and there is an increasing interest in chemoprevention to fight it. The authors sought a scientific rationale for the traditional use of six Cameroonian medicinal plants for the treatment of prostate inflammation/tumour. The prostate cells viability incubated with each ethanolic plant extract was determined after 24, 48 and 72 h using the MTT assay. The antitumor mechanisms of promising extracts [Treculia africana (TA) and Entandrophragma angolense (EA)] were further assessed by evaluating cell growth, cell proliferation, cell cycle, cell death mechanisms and cell migration. Only TA and EA significantly inhibited LNCaP, DU145 and PC3 prostate carcinoma cells growth and proliferation at the optimal concentrations (20–50 μg/mL). Furthermore, they significantly increased the number of apoptotic cells in PC3 cells at 20 μg/mL, while only TA significantly increased the number of G0/G1 cells in both DU145 and PC3 at 50 μg/mL. Cell cycle proteins (pcdk1, cdk2, pcdk2) were down-regulated by TA in both DU145 and PC3 cells. EA induced an overexpression of caspase-3 in both tested cells; meanwhile it induced an underexpression of cdk2. Apoptosis-related proteins Akt, pAkt and Bcl-2 were down-regulated in both DU145 and PC3 cells while caspase-3 was up-regulated following treatment with EA and TA. TA and EA inhibited cell chemotaxis and migration, while it increased cell adhesion to a fibronectin matrix. Taken altogether, these findings suggest that Treculia africana and Entandrophragma angolense might contain phyto-constituents which can be a promising strategy for the treatment of prostate cancer.
AB - Prostate cancer is the second leading cause of cancer deaths in men and there is an increasing interest in chemoprevention to fight it. The authors sought a scientific rationale for the traditional use of six Cameroonian medicinal plants for the treatment of prostate inflammation/tumour. The prostate cells viability incubated with each ethanolic plant extract was determined after 24, 48 and 72 h using the MTT assay. The antitumor mechanisms of promising extracts [Treculia africana (TA) and Entandrophragma angolense (EA)] were further assessed by evaluating cell growth, cell proliferation, cell cycle, cell death mechanisms and cell migration. Only TA and EA significantly inhibited LNCaP, DU145 and PC3 prostate carcinoma cells growth and proliferation at the optimal concentrations (20–50 μg/mL). Furthermore, they significantly increased the number of apoptotic cells in PC3 cells at 20 μg/mL, while only TA significantly increased the number of G0/G1 cells in both DU145 and PC3 at 50 μg/mL. Cell cycle proteins (pcdk1, cdk2, pcdk2) were down-regulated by TA in both DU145 and PC3 cells. EA induced an overexpression of caspase-3 in both tested cells; meanwhile it induced an underexpression of cdk2. Apoptosis-related proteins Akt, pAkt and Bcl-2 were down-regulated in both DU145 and PC3 cells while caspase-3 was up-regulated following treatment with EA and TA. TA and EA inhibited cell chemotaxis and migration, while it increased cell adhesion to a fibronectin matrix. Taken altogether, these findings suggest that Treculia africana and Entandrophragma angolense might contain phyto-constituents which can be a promising strategy for the treatment of prostate cancer.
KW - Apoptosis
KW - Cell cycle
KW - Cell invasion
KW - Ethnomedicinal plants
KW - Prostate cancer cells
UR - http://www.scopus.com/inward/record.url?scp=85104108388&partnerID=8YFLogxK
U2 - 10.1016/j.hermed.2021.100443
DO - 10.1016/j.hermed.2021.100443
M3 - Article
AN - SCOPUS:85104108388
SN - 2210-8033
VL - 28
JO - Journal of Herbal Medicine
JF - Journal of Herbal Medicine
M1 - 100443
ER -