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Updated: Aug 8, 2026

Application of Genetically Encoded Fluorescent Nitric Oxide (NO•) Probes, the geNOps, for Real-time Imaging of NO• Signals in Single Cells
Published on: March 16, 2017
Altered expression of key cellular gene products accompanies development of resistance to nitric oxide
Miguel Aguilar-Santelises1, Marlene Mozart, Richard Scuderi
1Department of Medicine, Division of Hematology, Karolinska University Hospital, Stockholm, Sweden.
Abstract:
NALM-6 is a pre-B leukemia cell line sensitive to exogenous nitric oxide (NO), which enters into apoptosis during 24 h of exposure to low doses of the NO donors SNAP (100 microM) or DETA-NO (250 microM). By culturing NALM-6 with repeated and increasing concentrations of SNAP, we obtained a variant (NALM-6R) that retains >95% viability and does not enter into apoptosis during 24 h culture in the presence of up to 500 microM SNAP or 750 microM DETA-NO. A power blot screen performed with 277 antibodies on cell lysates from NALM-6 and NALM-6R cultured without NO donors served to determine the altered constitutive expression of 19 proteins in NALM-6R. Proteins affected in the less sensitive cell line NALM6-R are involved in the regulation of apoptosis, the cell cycle, cell interactions, signal transduction, cell morphology, and cell motility. This model shows that repeated exposure of tumor cells to NO may either select NO-resistant cells or contribute to NO-sensitive conversion into NO-resistant cells. The identification of the proteins that are affected during this transition may help us to define the mechanisms that are involved in cell resistance to NO-cytotoxicity which often accompany clinical progression.
Insights
Researchers developed a nitric oxide (NO)-resistant leukemia cell line (NALM-6R) from a sensitive parent line (NALM-6). This NO resistance is linked to altered protein expression, offering insights into cancer cell survival mechanisms.
Area of Science:
- Cell Biology
- Cancer Research
- Biochemistry
Background:
- Nitric oxide (NO) induces apoptosis in sensitive leukemia cells.
- Developing resistance to NO is crucial for cancer cell survival and progression.
Purpose of the Study:
- To generate and characterize a nitric oxide (NO)-resistant leukemia cell line.
- To identify molecular mechanisms underlying NO resistance in cancer cells.
Main Methods:
- Culturing NALM-6 cells with increasing concentrations of NO donors (SNAP, DETA-NO) to obtain a resistant variant (NALM-6R).
- Utilizing a power blot screen with 277 antibodies to compare protein expression between NALM-6 and NALM-6R cells.
Main Results:
- NALM-6R cells exhibited >95% viability and resistance to NO-induced apoptosis.
- 19 proteins with altered constitutive expression were identified in NALM-6R cells.
- Affected proteins regulate apoptosis, cell cycle, cell interactions, signal transduction, morphology, and motility.
Conclusions:
- Repeated NO exposure can select for or induce NO-resistant tumor cells.
- Identifying altered proteins provides targets for understanding and overcoming NO resistance in cancer therapy.
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