Abstract |
Retroviral transformation has been associated with pro-proliferative oncogenic signaling in human cells. The current study demonstrates that transduction of human breast carcinoma cells (MDA-MB231) with LXSN and QCXIP retroviral vectors causes significant increases in growth rate, clonogenic fraction, and aldehyde dehydrogenase-1 positive cells (ALDH1+), which is associated with increased steady-state levels of cancer stem cell populations. Furthermore, this retroviral-induced enhancement of cancer cell growth in vitro was also accompanied by a significant increase in xenograft tumor growth rate in vivo. The retroviral induced increases in cancer cell growth rate were partially inhibited by treatment with 100 U/ml polyethylene glycol-conjugated-(PEG)- superoxide dismutase and/or PEG-catalase. These results show that retroviral infection of MDA-MB231 human breast cancer cells is capable of enhancing cell proliferation and cancer stem cell populations as well as suggesting that modulation of reactive oxygen species-induced pro-survival signaling pathways may be involved in these effects.
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Authors | Lauren J Wegman-Points, Melissa L T Teoh-Fitzgerald, Gaowei Mao, Yueming Zhu, Melissa A Fath, Douglas R Spitz, Frederick E Domann |
Journal | Redox biology
(Redox Biol)
Vol. 2
Pg. 847-54
( 2014)
ISSN: 2213-2317 [Print] Netherlands |
PMID | 25009786
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Isoenzymes
- catalase-polyethylene glycol
- Polyethylene Glycols
- Catalase
- Superoxide Dismutase
- polyoxyethylene-superoxide dismutase
- Aldehyde Dehydrogenase 1 Family
- ALDH1A1 protein, human
- ALDH1A1 protein, mouse
- Retinal Dehydrogenase
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Topics |
- Aldehyde Dehydrogenase 1 Family
- Animals
- Breast Neoplasms
(enzymology, pathology, virology)
- Catalase
(pharmacology)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Female
- Humans
- Isoenzymes
(metabolism)
- Mice
- Mice, Nude
- Neoplastic Stem Cells
(cytology, enzymology, virology)
- Polyethylene Glycols
(pharmacology)
- Retinal Dehydrogenase
(metabolism)
- Retroviridae
(physiology)
- Superoxide Dismutase
(pharmacology)
- Transplantation, Heterologous
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