1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately

Cancer or malignant tumors has a high death frequency in many countries. Nowadays many research facilities are dedicated to find new substances and techniques which would lead to better cancer therapies. Seven years ago a research team from Finland made a remarkable connection between vitamin D defi...

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Main Author: Kjellerås, Jennifer
Format: Others
Language:English
Published: Högskolan i Skövde, Institutionen för vård och natur 2007
Subjects:
Online Access:http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-474
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spelling ndltd-UPSALLA1-oai-DiVA.org-his-4742018-01-13T05:14:13Z1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separatelyengKjellerås, JenniferHögskolan i Skövde, Institutionen för vård och naturSkövde : Institutionen för vård och natur2007prostate cancervitamin D1.25(OH)2D324.25(OH)2D3growth inhibitionapoptosisantiproliferationMicrobiology in the medical areaMikrobiologi inom det medicinska områdetCancer or malignant tumors has a high death frequency in many countries. Nowadays many research facilities are dedicated to find new substances and techniques which would lead to better cancer therapies. Seven years ago a research team from Finland made a remarkable connection between vitamin D deficiencies and an increased chance of getting prostate cancer. The research investigating this statement has lead to findings of a new non-classical effect of the calcium controlling vitamin, 1,25(OH)2D3. This effect involves anti-proliferatory effects and more importantly apoptotic effects resulting in the hope of finding a new drug that can cure prostate cancer with the smallest amount of harm to the body. In an attempt to find out if the signalling pathway of this apoptotic effect is fast or slow, an experiment designed to detect when the apoptotic protein caspase-3 is induced has been performed. Cells from the cell line LNCaP has been cultured and incubated with 1,25(OH)2D3 and after 0min - 48h an assay was performed to detect the relative amounts of caspase-3 present in every sample. The optimal time period (48h) was then subjected to three different concentrations of 1,25(OH)2D3 and read in the same way as the previous samples. The results showed an increase in caspase-3 expression as early as 2 min, but disappear to be seen again at 24h and are more profound in 48h samples. The caspase-3 expression was also seen to form a possible exponential curve in dose-response. Student thesisinfo:eu-repo/semantics/bachelorThesistexthttp://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-474application/pdfinfo:eu-repo/semantics/openAccess
collection NDLTD
language English
format Others
sources NDLTD
topic prostate cancer
vitamin D
1.25(OH)2D3
24.25(OH)2D3
growth inhibition
apoptosis
antiproliferation
Microbiology in the medical area
Mikrobiologi inom det medicinska området
spellingShingle prostate cancer
vitamin D
1.25(OH)2D3
24.25(OH)2D3
growth inhibition
apoptosis
antiproliferation
Microbiology in the medical area
Mikrobiologi inom det medicinska området
Kjellerås, Jennifer
1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately
description Cancer or malignant tumors has a high death frequency in many countries. Nowadays many research facilities are dedicated to find new substances and techniques which would lead to better cancer therapies. Seven years ago a research team from Finland made a remarkable connection between vitamin D deficiencies and an increased chance of getting prostate cancer. The research investigating this statement has lead to findings of a new non-classical effect of the calcium controlling vitamin, 1,25(OH)2D3. This effect involves anti-proliferatory effects and more importantly apoptotic effects resulting in the hope of finding a new drug that can cure prostate cancer with the smallest amount of harm to the body. In an attempt to find out if the signalling pathway of this apoptotic effect is fast or slow, an experiment designed to detect when the apoptotic protein caspase-3 is induced has been performed. Cells from the cell line LNCaP has been cultured and incubated with 1,25(OH)2D3 and after 0min - 48h an assay was performed to detect the relative amounts of caspase-3 present in every sample. The optimal time period (48h) was then subjected to three different concentrations of 1,25(OH)2D3 and read in the same way as the previous samples. The results showed an increase in caspase-3 expression as early as 2 min, but disappear to be seen again at 24h and are more profound in 48h samples. The caspase-3 expression was also seen to form a possible exponential curve in dose-response.
author Kjellerås, Jennifer
author_facet Kjellerås, Jennifer
author_sort Kjellerås, Jennifer
title 1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately
title_short 1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately
title_full 1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately
title_fullStr 1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately
title_full_unstemmed 1,25(OH)2D3 increase caspase-3 activity in LNCaP cells after 2 minutes and 48h separately
title_sort 1,25(oh)2d3 increase caspase-3 activity in lncap cells after 2 minutes and 48h separately
publisher Högskolan i Skövde, Institutionen för vård och natur
publishDate 2007
url http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-474
work_keys_str_mv AT kjellerasjennifer 125oh2d3increasecaspase3activityinlncapcellsafter2minutesand48hseparately
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