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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Published in:Biochimica et biophysica acta Vol. 1780; no. 4; pp. 673 - 679
Main Authors: Kunwar, A., Barik, A., Mishra, B., Rathinasamy, K., Pandey, R., Priyadarsini, K.I.
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 01.04.2008
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ISSN:0304-4165, 0006-3002, 1872-8006
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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.
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
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  surname: Kunwar
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  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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ISSN 0304-4165
0006-3002
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IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Fluorescence
Cytotoxicity
Cellular uptake
Curcumin
Nuclear localization
Tumor cell
Language English
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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
URI https://dx.doi.org/10.1016/j.bbagen.2007.11.016
https://www.ncbi.nlm.nih.gov/pubmed/18178166
https://www.proquest.com/docview/70440225
Volume 1780
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