Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-26T07:21:59.185Z Has data issue: false hasContentIssue false

Androgen-Responsive Lncap and Androgen-Independent Du145 Prostate Cancer Cells Display Different Taxol Sensitivities

Published online by Cambridge University Press:  02 July 2020

Maureen Ripple
Affiliation:
institute on Aging, and Comprehensive Cancer Center, Dept. of Medicine, Univ. of Wisconsin, and the William S. Middleton Veterans Administr. Hospital, Madison, WI53792
Meghan Taylo
Affiliation:
Dept. of Veterinary Pathobiology, University of Missouri-Columbia, Columbia, MO65211
Chris Huese
Affiliation:
Dept. of Veterinary Pathobiology, University of Missouri-Columbia, Columbia, MO65211 Cancer Research Center, Columbia, MO65211
Heide Schatte
Affiliation:
Dept. of Veterinary Pathobiology, University of Missouri-Columbia, Columbia, MO65211 Cancer Research Center, Columbia, MO65211
Get access

Extract

Taxol has been used as anti-cancer compound against prostate, ovarian, and metastatic breast cancer. While the most obvious effect of taxol is bundeling of microtubules and mitotic arrest, recent studies have demonstrated that taxol is able to induce intranucleosomal DNA fragmentation and typical morphological features of apoptosis in a number of solid tumor cells. These results indicate that taxol may exert its anti-tumor effects via secondary mechanisms which may or may not be related to its primary effects on microtubules. It has been shown that taxol-induced microtubular changes and G2/M arrest are associated with the release of the electron transfer protein cytochrome C from mitochondria into the cytosol. Cytochrome C then binds to APAF-1 (a human homolog of the ced-4 gene of C. elegans), which binds, cleaves, and activates caspase- 9, ultimately resulting in the cleavage and activity of caspase-3. We investigated the effects of taxol (100nM) on microtubules, on DNA, and on the pre-apoptotic mitochondrial events using LNCaP and DU145 prostate cancer cells.

Type
Biomedical Applications
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Bhalla, K.Proceedings MSA (1998) 56(4)2, 10401041.Google Scholar
2.Ripple, M. et al., Cancer Res. (1997) 57, 24282433.Google Scholar
3.Ripple, M. et al., J. Natl. Cancer Inst. (1997) 89, 1, 4048.CrossRefGoogle Scholar
4.Schatten, H., et al., Cell Tissue Res. (1998) 294, 525535.CrossRefGoogle Scholar