Quantitative cellular uptake, localization and cytotoxicity of curcumin in normal and tumor cells
Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from Curcuma longa, was calculated in two types of normal cells: spleen lymphocytes, and NIH3T3 and two tumor cell lines: EL4 and MCF7. Both the uptake and fluoresce...
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| Vydáno v: | Biochimica et biophysica acta Ročník 1780; číslo 4; s. 673 - 679 |
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| Hlavní autoři: | , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Netherlands
Elsevier B.V
01.04.2008
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| Témata: | |
| ISSN: | 0304-4165, 0006-3002, 1872-8006 |
| On-line přístup: | Získat plný text |
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| Abstract | Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from
Curcuma longa, was calculated in two types of normal cells: spleen lymphocytes, and NIH3T3 and two tumor cell lines: EL4 and MCF7. Both the uptake and fluorescence intensity of curcumin were significantly higher in tumor cells compared to the normal cells. A linear dependency on the uptake was observed with treatment concentration of curcumin. Using laser confocal microscopy, intracellular localization of curcumin was monitored and the results indicated that curcumin is located both in the cell membrane and the nucleus. Sub-cellular fractionation of curcumin-loaded MCF7 cells supported the differential distribution of curcumin in membrane, cytoplasm and nuclear compartments of cell with maximum localization in the membrane. Cytotoxicity studies in different cell lines indicated that the toxicity of curcumin increased with increasing uptake. |
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| AbstractList | Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from Curcuma longa, was calculated in two types of normal cells: spleen lymphocytes, and NIH3T3 and two tumor cell lines: EL4 and MCF7. Both the uptake and fluorescence intensity of curcumin were significantly higher in tumor cells compared to the normal cells. A linear dependency on the uptake was observed with treatment concentration of curcumin. Using laser confocal microscopy, intracellular localization of curcumin was monitored and the results indicated that curcumin is located both in the cell membrane and the nucleus. Sub-cellular fractionation of curcumin-loaded MCF7 cells supported the differential distribution of curcumin in membrane, cytoplasm and nuclear compartments of cell with maximum localization in the membrane. Cytotoxicity studies in different cell lines indicated that the toxicity of curcumin increased with increasing uptake.Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from Curcuma longa, was calculated in two types of normal cells: spleen lymphocytes, and NIH3T3 and two tumor cell lines: EL4 and MCF7. Both the uptake and fluorescence intensity of curcumin were significantly higher in tumor cells compared to the normal cells. A linear dependency on the uptake was observed with treatment concentration of curcumin. Using laser confocal microscopy, intracellular localization of curcumin was monitored and the results indicated that curcumin is located both in the cell membrane and the nucleus. Sub-cellular fractionation of curcumin-loaded MCF7 cells supported the differential distribution of curcumin in membrane, cytoplasm and nuclear compartments of cell with maximum localization in the membrane. Cytotoxicity studies in different cell lines indicated that the toxicity of curcumin increased with increasing uptake. Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from Curcuma longa, was calculated in two types of normal cells: spleen lymphocytes, and NIH3T3 and two tumor cell lines: EL4 and MCF7. Both the uptake and fluorescence intensity of curcumin were significantly higher in tumor cells compared to the normal cells. A linear dependency on the uptake was observed with treatment concentration of curcumin. Using laser confocal microscopy, intracellular localization of curcumin was monitored and the results indicated that curcumin is located both in the cell membrane and the nucleus. Sub-cellular fractionation of curcumin-loaded MCF7 cells supported the differential distribution of curcumin in membrane, cytoplasm and nuclear compartments of cell with maximum localization in the membrane. Cytotoxicity studies in different cell lines indicated that the toxicity of curcumin increased with increasing uptake. Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from Curcuma longa, was calculated in two types of normal cells: spleen lymphocytes, and NIH3T3 and two tumor cell lines: EL4 and MCF7. Both the uptake and fluorescence intensity of curcumin were significantly higher in tumor cells compared to the normal cells. A linear dependency on the uptake was observed with treatment concentration of curcumin. Using laser confocal microscopy, intracellular localization of curcumin was monitored and the results indicated that curcumin is located both in the cell membrane and the nucleus. Sub-cellular fractionation of curcumin-loaded MCF7 cells supported the differential distribution of curcumin in membrane, cytoplasm and nuclear compartments of cell with maximum localization in the membrane. Cytotoxicity studies in different cell lines indicated that the toxicity of curcumin increased with increasing uptake. |
| Author | Pandey, R. Mishra, B. Barik, A. Rathinasamy, K. Priyadarsini, K.I. Kunwar, A. |
| Author_xml | – sequence: 1 givenname: A. surname: Kunwar fullname: Kunwar, A. organization: Radiation and Photochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India – sequence: 2 givenname: A. surname: Barik fullname: Barik, A. organization: Radiation and Photochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India – sequence: 3 givenname: B. surname: Mishra fullname: Mishra, B. organization: Radiation and Photochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India – sequence: 4 givenname: K. surname: Rathinasamy fullname: Rathinasamy, K. organization: School of Biosciences and Bioengineering, IIT-Bombay, Mumbai, 400 076, India – sequence: 5 givenname: R. surname: Pandey fullname: Pandey, R. organization: Radiation Biology and Health Sciences Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India – sequence: 6 givenname: K.I. surname: Priyadarsini fullname: Priyadarsini, K.I. email: kindira@barc.gov.in organization: Radiation and Photochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18178166$$D View this record in MEDLINE/PubMed |
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| Snippet | Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from
Curcuma longa, was... Using absorption and fluorescence spectroscopic methods, quantitative cellular uptake of curcumin, an antioxidant and anti-tumor agent from Curcuma longa, was... |
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| SubjectTerms | Animals Biological Transport Cell Line, Tumor Cell Membrane - metabolism Cell Nucleus - metabolism Cell Survival - drug effects Cells, Cultured Cellular uptake Curcuma - chemistry Curcumin Curcumin - metabolism Curcumin - pharmacokinetics Curcumin - pharmacology Cytotoxicity Dose-Response Relationship, Drug Fluorescence Humans Lymphocytes - cytology Lymphocytes - drug effects Lymphocytes - metabolism Mice Microscopy, Confocal NIH 3T3 Cells Nuclear localization Spectrometry, Fluorescence Time Factors Tumor cell |
| Title | Quantitative cellular uptake, localization and cytotoxicity of curcumin in normal and tumor cells |
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