Apoptotic activity of ursolic acid may correlate with the inhibition of initiation of DNA replication

Dong Kyoo Kim, Jin Hyen Baek, Chang Mo Kang, Mi Ae Yoo, Jae Wook Sung, Dong Kil Kim, Hae Young Chung, Nam Deuk Kim, Yung Hyun Choi, Suk-Hee Lee, Kyu Won Kim

Research output: Contribution to journalArticle

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Abstract

Ursolic acid (UA), a pentacyclic triterpene acid, has been reported to exhibit anti-tumor activity. In this study, we investigated the pro-apoptotic effect of UA on HepG2 human hepatoblastoma cells. Treatment with UA decreased the viability of HepG2 cells in a concentration- and time-dependent manner. Furthermore, 30 μM of UA induced DNA fragmentation and subdiploid cells and enhanced the release of cytochrome c and the activation of caspase-3. These resuets suggest that UA induces cell death through apoptosis, which may be mediated by cytochrome c-dependent caspase-3 activation. In addition, cell-cycle analysis revealed that UA-treated cells were arrested predominantly in the G(o) and G(l) phases with a concomitant decrease in the cell population of $ phase. Pioreover, expression of p21(WAF1) , a cell-cycle regulator, was increased by UA, indicating that p21(WAF1) might mediate UA-induced cell-cycle arrest. However, UA markedly inhibited SV40 DNA replication in the initiation stage in vitro and significantly reduced the DNA cleaving of topoisomerase I and the ssDNA binding activity of replication protein A. These results indicate that the inhibition of DNA replication by UA may result from blockade of the establishment of the replication fork during initiation stage, consequently contributing to UA-induced cell-cycle arrest. Taken together, we suggest that UA-induced cell-cycle arrest may be mediated by inhibition of DNA replication and the increase of p21(WAF1) expression, which induces the release of cytochrome c and the activation of caspase-3, leading to apoptosis of HepG2 cells. Int J. Cancer 87:629-636, 2000. (C) 2000 Wiley-Liss, Inc.

Original languageEnglish
Pages (from-to)629-636
Number of pages8
JournalInternational Journal of Cancer
Volume87
Issue number5
DOIs
StatePublished - 2000

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DNA Replication
Cell Cycle Checkpoints
Cytochromes c
Caspase 3
Hep G2 Cells
ursolic acid
Cell Cycle
Pentacyclic Triterpenes
Replication Protein A
Apoptosis
Hepatoblastoma
Type I DNA Topoisomerase
DNA Fragmentation
Neoplasms
Cell Death
Acids

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Apoptotic activity of ursolic acid may correlate with the inhibition of initiation of DNA replication. / Kim, Dong Kyoo; Baek, Jin Hyen; Kang, Chang Mo; Yoo, Mi Ae; Sung, Jae Wook; Kim, Dong Kil; Chung, Hae Young; Kim, Nam Deuk; Choi, Yung Hyun; Lee, Suk-Hee; Kim, Kyu Won.

In: International Journal of Cancer, Vol. 87, No. 5, 2000, p. 629-636.

Research output: Contribution to journalArticle

Kim, DK, Baek, JH, Kang, CM, Yoo, MA, Sung, JW, Kim, DK, Chung, HY, Kim, ND, Choi, YH, Lee, S-H & Kim, KW 2000, 'Apoptotic activity of ursolic acid may correlate with the inhibition of initiation of DNA replication', International Journal of Cancer, vol. 87, no. 5, pp. 629-636. https://doi.org/10.1002/1097-0215(20000901)87:5<629::AID-IJC2>3.0.CO;2-P
Kim, Dong Kyoo ; Baek, Jin Hyen ; Kang, Chang Mo ; Yoo, Mi Ae ; Sung, Jae Wook ; Kim, Dong Kil ; Chung, Hae Young ; Kim, Nam Deuk ; Choi, Yung Hyun ; Lee, Suk-Hee ; Kim, Kyu Won. / Apoptotic activity of ursolic acid may correlate with the inhibition of initiation of DNA replication. In: International Journal of Cancer. 2000 ; Vol. 87, No. 5. pp. 629-636.
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abstract = "Ursolic acid (UA), a pentacyclic triterpene acid, has been reported to exhibit anti-tumor activity. In this study, we investigated the pro-apoptotic effect of UA on HepG2 human hepatoblastoma cells. Treatment with UA decreased the viability of HepG2 cells in a concentration- and time-dependent manner. Furthermore, 30 μM of UA induced DNA fragmentation and subdiploid cells and enhanced the release of cytochrome c and the activation of caspase-3. These resuets suggest that UA induces cell death through apoptosis, which may be mediated by cytochrome c-dependent caspase-3 activation. In addition, cell-cycle analysis revealed that UA-treated cells were arrested predominantly in the G(o) and G(l) phases with a concomitant decrease in the cell population of $ phase. Pioreover, expression of p21(WAF1) , a cell-cycle regulator, was increased by UA, indicating that p21(WAF1) might mediate UA-induced cell-cycle arrest. However, UA markedly inhibited SV40 DNA replication in the initiation stage in vitro and significantly reduced the DNA cleaving of topoisomerase I and the ssDNA binding activity of replication protein A. These results indicate that the inhibition of DNA replication by UA may result from blockade of the establishment of the replication fork during initiation stage, consequently contributing to UA-induced cell-cycle arrest. Taken together, we suggest that UA-induced cell-cycle arrest may be mediated by inhibition of DNA replication and the increase of p21(WAF1) expression, which induces the release of cytochrome c and the activation of caspase-3, leading to apoptosis of HepG2 cells. Int J. Cancer 87:629-636, 2000. (C) 2000 Wiley-Liss, Inc.",
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T1 - Apoptotic activity of ursolic acid may correlate with the inhibition of initiation of DNA replication

AU - Kim, Dong Kyoo

AU - Baek, Jin Hyen

AU - Kang, Chang Mo

AU - Yoo, Mi Ae

AU - Sung, Jae Wook

AU - Kim, Dong Kil

AU - Chung, Hae Young

AU - Kim, Nam Deuk

AU - Choi, Yung Hyun

AU - Lee, Suk-Hee

AU - Kim, Kyu Won

PY - 2000

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N2 - Ursolic acid (UA), a pentacyclic triterpene acid, has been reported to exhibit anti-tumor activity. In this study, we investigated the pro-apoptotic effect of UA on HepG2 human hepatoblastoma cells. Treatment with UA decreased the viability of HepG2 cells in a concentration- and time-dependent manner. Furthermore, 30 μM of UA induced DNA fragmentation and subdiploid cells and enhanced the release of cytochrome c and the activation of caspase-3. These resuets suggest that UA induces cell death through apoptosis, which may be mediated by cytochrome c-dependent caspase-3 activation. In addition, cell-cycle analysis revealed that UA-treated cells were arrested predominantly in the G(o) and G(l) phases with a concomitant decrease in the cell population of $ phase. Pioreover, expression of p21(WAF1) , a cell-cycle regulator, was increased by UA, indicating that p21(WAF1) might mediate UA-induced cell-cycle arrest. However, UA markedly inhibited SV40 DNA replication in the initiation stage in vitro and significantly reduced the DNA cleaving of topoisomerase I and the ssDNA binding activity of replication protein A. These results indicate that the inhibition of DNA replication by UA may result from blockade of the establishment of the replication fork during initiation stage, consequently contributing to UA-induced cell-cycle arrest. Taken together, we suggest that UA-induced cell-cycle arrest may be mediated by inhibition of DNA replication and the increase of p21(WAF1) expression, which induces the release of cytochrome c and the activation of caspase-3, leading to apoptosis of HepG2 cells. Int J. Cancer 87:629-636, 2000. (C) 2000 Wiley-Liss, Inc.

AB - Ursolic acid (UA), a pentacyclic triterpene acid, has been reported to exhibit anti-tumor activity. In this study, we investigated the pro-apoptotic effect of UA on HepG2 human hepatoblastoma cells. Treatment with UA decreased the viability of HepG2 cells in a concentration- and time-dependent manner. Furthermore, 30 μM of UA induced DNA fragmentation and subdiploid cells and enhanced the release of cytochrome c and the activation of caspase-3. These resuets suggest that UA induces cell death through apoptosis, which may be mediated by cytochrome c-dependent caspase-3 activation. In addition, cell-cycle analysis revealed that UA-treated cells were arrested predominantly in the G(o) and G(l) phases with a concomitant decrease in the cell population of $ phase. Pioreover, expression of p21(WAF1) , a cell-cycle regulator, was increased by UA, indicating that p21(WAF1) might mediate UA-induced cell-cycle arrest. However, UA markedly inhibited SV40 DNA replication in the initiation stage in vitro and significantly reduced the DNA cleaving of topoisomerase I and the ssDNA binding activity of replication protein A. These results indicate that the inhibition of DNA replication by UA may result from blockade of the establishment of the replication fork during initiation stage, consequently contributing to UA-induced cell-cycle arrest. Taken together, we suggest that UA-induced cell-cycle arrest may be mediated by inhibition of DNA replication and the increase of p21(WAF1) expression, which induces the release of cytochrome c and the activation of caspase-3, leading to apoptosis of HepG2 cells. Int J. Cancer 87:629-636, 2000. (C) 2000 Wiley-Liss, Inc.

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