Novel anti-apoptotic effect of the retinoblastoma protein: implications for polyamine analogue toxicity.
(2012) In Amino Acids 42. p.929-937- Abstract
- The retinoblastoma protein (pRb) pathway is frequently altered in breast cancer cells. pRb is involved in the regulation of cell proliferation and cell death. The breast cancer cell line L56Br-C1 does not express pRb and is extremely sensitive to treatment with the polyamine analogue N (1),N (11)-diethylnorspermine (DENSPM) which causes apoptosis. Polyamines are essential for the regulation of cell proliferation, cell differentiation and cell death. DENSPM depletes cells of polyamines, e.g., by inducing the activity of the polyamine catabolic enzyme spermidine/spermine N (1)-acetyltransferase (SSAT). In this study, L56Br-C1 cells were transfected with human pRb-cDNA. Overexpression of pRb inhibited DENSPM-induced cell death and... (More)
- The retinoblastoma protein (pRb) pathway is frequently altered in breast cancer cells. pRb is involved in the regulation of cell proliferation and cell death. The breast cancer cell line L56Br-C1 does not express pRb and is extremely sensitive to treatment with the polyamine analogue N (1),N (11)-diethylnorspermine (DENSPM) which causes apoptosis. Polyamines are essential for the regulation of cell proliferation, cell differentiation and cell death. DENSPM depletes cells of polyamines, e.g., by inducing the activity of the polyamine catabolic enzyme spermidine/spermine N (1)-acetyltransferase (SSAT). In this study, L56Br-C1 cells were transfected with human pRb-cDNA. Overexpression of pRb inhibited DENSPM-induced cell death and DENSPM-induced SSAT activity. This suggests that the pRb protein level is a promising marker for polyamine depletion sensitivity and that there is a connection between pRb and the regulation of SSAT activity. We also show that SSAT protein levels and SSAT activity do not always correlate, suggesting that there is an unknown regulation of SSAT (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2151616
- author
- Johansson, Veronica LU ; Thuvesson, Iréne LU ; Alm, Kersti LU and Oredsson, Stina LU
- organization
- publishing date
- 2012
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Amino Acids
- volume
- 42
- pages
- 929 - 937
- publisher
- Springer
- external identifiers
-
- wos:000299506000049
- pmid:21809081
- scopus:84861657647
- ISSN
- 0939-4451
- DOI
- 10.1007/s00726-011-1007-y
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Division of Hematology and Transfusion Medicine (013041100), Animal Physiology (Closed 2011) (011011000), Functional Zoology (432112239), Molecular Cell Biology (432112241)
- id
- 38d0b841-32e1-44b2-93c7-406fde202871 (old id 2151616)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/21809081?dopt=Abstract
- date added to LUP
- 2016-04-04 07:04:03
- date last changed
- 2024-07-01 11:25:20
@article{38d0b841-32e1-44b2-93c7-406fde202871, abstract = {{The retinoblastoma protein (pRb) pathway is frequently altered in breast cancer cells. pRb is involved in the regulation of cell proliferation and cell death. The breast cancer cell line L56Br-C1 does not express pRb and is extremely sensitive to treatment with the polyamine analogue N (1),N (11)-diethylnorspermine (DENSPM) which causes apoptosis. Polyamines are essential for the regulation of cell proliferation, cell differentiation and cell death. DENSPM depletes cells of polyamines, e.g., by inducing the activity of the polyamine catabolic enzyme spermidine/spermine N (1)-acetyltransferase (SSAT). In this study, L56Br-C1 cells were transfected with human pRb-cDNA. Overexpression of pRb inhibited DENSPM-induced cell death and DENSPM-induced SSAT activity. This suggests that the pRb protein level is a promising marker for polyamine depletion sensitivity and that there is a connection between pRb and the regulation of SSAT activity. We also show that SSAT protein levels and SSAT activity do not always correlate, suggesting that there is an unknown regulation of SSAT}}, author = {{Johansson, Veronica and Thuvesson, Iréne and Alm, Kersti and Oredsson, Stina}}, issn = {{0939-4451}}, language = {{eng}}, pages = {{929--937}}, publisher = {{Springer}}, series = {{Amino Acids}}, title = {{Novel anti-apoptotic effect of the retinoblastoma protein: implications for polyamine analogue toxicity.}}, url = {{http://dx.doi.org/10.1007/s00726-011-1007-y}}, doi = {{10.1007/s00726-011-1007-y}}, volume = {{42}}, year = {{2012}}, }