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Plasma protein carbonyl levels and breast cancer risk

To study the role of oxidative stress in breast cancer risk, we analysed plasma levels of protein carbonyls in 1050 cases and 1107 controls. We found a statistically significant trend in breast cancer risk in relation to increasing quartiles of plasma protein carbonyl levels (OR = 1.2, 95% CI = 0.9–...

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Autores principales: Rossner, Pavel, Terry, Mary Beth, Gammon, Marilie D, Agrawal, Meenakshi, Zhang, Fang Fang, Ferris, Jennifer S, Teitelbaum, Susan L, Eng, Sybil M, Gaudet, Mia M, Neugut, Alfred I, Santella, Regina M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401280/
https://www.ncbi.nlm.nih.gov/pubmed/17979889
http://dx.doi.org/10.1111/j.1582-4934.2007.00097.x
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author Rossner, Pavel
Terry, Mary Beth
Gammon, Marilie D
Agrawal, Meenakshi
Zhang, Fang Fang
Ferris, Jennifer S
Teitelbaum, Susan L
Eng, Sybil M
Gaudet, Mia M
Neugut, Alfred I
Santella, Regina M
author_facet Rossner, Pavel
Terry, Mary Beth
Gammon, Marilie D
Agrawal, Meenakshi
Zhang, Fang Fang
Ferris, Jennifer S
Teitelbaum, Susan L
Eng, Sybil M
Gaudet, Mia M
Neugut, Alfred I
Santella, Regina M
author_sort Rossner, Pavel
collection PubMed
description To study the role of oxidative stress in breast cancer risk, we analysed plasma levels of protein carbonyls in 1050 cases and 1107 controls. We found a statistically significant trend in breast cancer risk in relation to increasing quartiles of plasma protein carbonyl levels (OR = 1.2, 95% CI = 0.9–1.5; OR = 1.5, 95% CI = 1.2–2.0; OR = 1.6, 95% CI = 1.2–2.1, for the 2(nd), 3(rd) and 4(th) quartile relative to the lowest quartile, respectively, P for trend = 0.0001). The increase in risk was similar for younger (<50 years) and older women, more pronounced among women with higher physical activity levels (0.7 hrs/week for 4(th) quartile versus lowest quartile OR = 2.0, 95% CI = 1.4–3.0), higher alcohol consumption (≥15 grams/day for 4(th) quartile versus lowest quartile OR = 2.3, 95% CI = 1.1–4.7), and hormone replacement therapy use (HRT, OR = 2.6, 95% CI = 1.6–4.4 for 4(th) quartile versus lowest quartile). The multiplicative interaction terms were statistically significant only for physical activity and HRT. The positive association between plasma protein carbonyl levels and breast cancer risk was also observed when the analysis was restricted to women who had not received chemotherapy or radiation therapy prior to blood collection. Among controls, oxidized protein levels significantly increased with cigarette smoking and higher fruit and vegetable consumption, and decreased with alcohol consumption >30 grams per day. Women with higher levels of plasma protein carbonyl and urinary 15F(2t)-isoprostane had an 80% increase in breast cancer risk (OR = 1.8, 95% CI = 1.2–2.6) compared to women with levels below the median for both markers of oxidative stress. In summary, our results suggest that increased plasma protein carbonyl levels may be associated with breast cancer risk.
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spelling pubmed-44012802015-04-27 Plasma protein carbonyl levels and breast cancer risk Rossner, Pavel Terry, Mary Beth Gammon, Marilie D Agrawal, Meenakshi Zhang, Fang Fang Ferris, Jennifer S Teitelbaum, Susan L Eng, Sybil M Gaudet, Mia M Neugut, Alfred I Santella, Regina M J Cell Mol Med Articles To study the role of oxidative stress in breast cancer risk, we analysed plasma levels of protein carbonyls in 1050 cases and 1107 controls. We found a statistically significant trend in breast cancer risk in relation to increasing quartiles of plasma protein carbonyl levels (OR = 1.2, 95% CI = 0.9–1.5; OR = 1.5, 95% CI = 1.2–2.0; OR = 1.6, 95% CI = 1.2–2.1, for the 2(nd), 3(rd) and 4(th) quartile relative to the lowest quartile, respectively, P for trend = 0.0001). The increase in risk was similar for younger (<50 years) and older women, more pronounced among women with higher physical activity levels (0.7 hrs/week for 4(th) quartile versus lowest quartile OR = 2.0, 95% CI = 1.4–3.0), higher alcohol consumption (≥15 grams/day for 4(th) quartile versus lowest quartile OR = 2.3, 95% CI = 1.1–4.7), and hormone replacement therapy use (HRT, OR = 2.6, 95% CI = 1.6–4.4 for 4(th) quartile versus lowest quartile). The multiplicative interaction terms were statistically significant only for physical activity and HRT. The positive association between plasma protein carbonyl levels and breast cancer risk was also observed when the analysis was restricted to women who had not received chemotherapy or radiation therapy prior to blood collection. Among controls, oxidized protein levels significantly increased with cigarette smoking and higher fruit and vegetable consumption, and decreased with alcohol consumption >30 grams per day. Women with higher levels of plasma protein carbonyl and urinary 15F(2t)-isoprostane had an 80% increase in breast cancer risk (OR = 1.8, 95% CI = 1.2–2.6) compared to women with levels below the median for both markers of oxidative stress. In summary, our results suggest that increased plasma protein carbonyl levels may be associated with breast cancer risk. Blackwell Publishing Ltd 2007-09 2007-08-13 /pmc/articles/PMC4401280/ /pubmed/17979889 http://dx.doi.org/10.1111/j.1582-4934.2007.00097.x Text en
spellingShingle Articles
Rossner, Pavel
Terry, Mary Beth
Gammon, Marilie D
Agrawal, Meenakshi
Zhang, Fang Fang
Ferris, Jennifer S
Teitelbaum, Susan L
Eng, Sybil M
Gaudet, Mia M
Neugut, Alfred I
Santella, Regina M
Plasma protein carbonyl levels and breast cancer risk
title Plasma protein carbonyl levels and breast cancer risk
title_full Plasma protein carbonyl levels and breast cancer risk
title_fullStr Plasma protein carbonyl levels and breast cancer risk
title_full_unstemmed Plasma protein carbonyl levels and breast cancer risk
title_short Plasma protein carbonyl levels and breast cancer risk
title_sort plasma protein carbonyl levels and breast cancer risk
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401280/
https://www.ncbi.nlm.nih.gov/pubmed/17979889
http://dx.doi.org/10.1111/j.1582-4934.2007.00097.x
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