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Genistein Induces Antiproliferative Activity and Apoptosis in Human Osteosarcoma Saos-2 Cells.
Hagiwara, Hiromi; Wako, Hana; Nakata, Kyoko; Aida, Rieko.
Affiliation
  • Hagiwara H; Department of Biomedical Engineering, Toin University of Yokohama, Yokohama, Japan hagiwara@toin.ac.jp.
  • Wako H; Department of Biomedical Engineering, Toin University of Yokohama, Yokohama, Japan.
  • Nakata K; Department of Biomedical Engineering, Toin University of Yokohama, Yokohama, Japan.
  • Aida R; Department of Biomedical Engineering, Toin University of Yokohama, Yokohama, Japan.
Anticancer Res ; 43(12): 5387-5392, 2023 Dec.
Article in En | MEDLINE | ID: mdl-38030209
ABSTRACT
BACKGROUND/

AIM:

Genistein (4', 5, 7-trihydroxyisoflavone) and daidzein (4', 7-dihydroxyisoflavone) are isoflavones derived from soybean and have anti-cancer effects in various cells. However, the effects of genistein and daidzein on the human osteosarcoma cell line Saos-2 has not been investigated before. MATERIALS AND

METHODS:

Human osteosarcoma Saos-2 cells were treated with genistein for 24 and 48 hours. Cytotoxicity and apoptosis were measured.

RESULTS:

Genistein significantly inhibited proliferation of Saos-2 cells stronger than daidzein in a dose-dependent manner (0 to 80 µM). Genistein also significantly suppressed Saos-2 cell viability in a dose-dependent manner (0 to 100 µM). In contrast, daidzein did not affect Saos-2 cell viability. Real-time PCR revealed that genistein caused G1-arrest by increasing the expression of p21 and p27 mRNAs in Saos-2 cells. In addition, genistein induced apoptosis through the up-regulation of effector caspase-3/7 activity in Saos-2 cells. Genistein also enhanced initiator caspase-9 and TNF-α mRNA expression in cells.

CONCLUSION:

Genistein may inhibit proliferation through the up-regulation of p21 and p27 and viability by inducing apoptosis in Saos-2 cells.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteosarcoma / Isoflavones Limits: Humans Language: En Journal: Anticancer Res Year: 2023 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteosarcoma / Isoflavones Limits: Humans Language: En Journal: Anticancer Res Year: 2023 Document type: Article Affiliation country: Japan