Matuszczak Milena, Kiljańczyk Adam, Marciniak Wojciech, Derkacz Róża, Stempa Klaudia, Baszuk Piotr, Bryśkiewicz Marta, Sun Ping, Cheriyan Angela, Cybulski Cezary, Dębniak Tadeusz, Gronwald Jacek, Huzarski Tomasz, Lener Marcin R, Jakubowska Anna, Szwiec Marek, Stawicka-Niełacna Małgorzata, Godlewski Dariusz, Prusaczyk Artur, Jasiewicz Andrzej, Kluz Tomasz, Tomiczek-Szwiec Joanna, Kilar-Kobierzycka Ewa, Siołek Monika, Wiśniowski Rafał, Posmyk Renata, Jarkiewicz-Tretyn Joanna, Scott Rodney J, Narod Steven A, Lubiński Jan
Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, ul. Unii Lubelskiej 1, 71-252 Szczecin, Poland.
Read-Gene, Grzepnica, ul. Alabastrowa 8, 72-003 Dobra, Poland.
Antioxidants (Basel). 2024 May 16;13(5):609. doi: 10.3390/antiox13050609.
BRCA1 mutations predispose women to breast and ovarian cancer. The anticancer effect of zinc is typically linked to its antioxidant abilities and protecting cells against oxidative stress. Zinc regulates key processes in cancer development, including DNA repair, gene expression, and apoptosis. We took a blood sample from 989 female BRCA1 mutation carriers who were initially unaffected by cancer and followed them for a mean of 7.5 years thereafter. There were 172 incident cases of cancer, including 121 cases of breast cancer, 29 cases of ovarian cancers, and 22 cancers at other sites. A zinc level in the lowest tertile was associated with a modestly higher risk of ovarian cancer compared to women with zinc levels in the upper two tertiles (HR = 1.65; 95% CI 0.80 to 3.44; = 0.18), but this was not significant. Among those women with zinc levels in the lowest tertile, the 10-year cumulative risk of ovarian cancer was 6.1%. Among those in the top two tertiles of zinc level, the ten-year cumulative risk of ovarian cancer was 4.7%. There was no significant association between zinc level and breast cancer risk. Our preliminary study does not support an association between serum zinc level and cancer risk in BRCA1 mutation carriers.
BRCA1基因突变使女性易患乳腺癌和卵巢癌。锌的抗癌作用通常与其抗氧化能力以及保护细胞免受氧化应激有关。锌调节癌症发展中的关键过程,包括DNA修复、基因表达和细胞凋亡。我们从989名最初未患癌症的女性BRCA1突变携带者中采集了血样,此后平均随访7.5年。有172例新发癌症病例,包括121例乳腺癌、29例卵巢癌和22例其他部位的癌症。与锌水平处于最高三分位数的女性相比,锌水平处于最低三分位数的女性患卵巢癌的风险略高(风险比=1.65;95%置信区间0.80至3.44;P=0.18),但这并不显著。在锌水平处于最低三分位数的女性中,卵巢癌的10年累积风险为6.1%。在锌水平处于最高两个三分位数的女性中,卵巢癌的10年累积风险为4.7%。锌水平与乳腺癌风险之间无显著关联。我们的初步研究不支持血清锌水平与BRCA1突变携带者癌症风险之间存在关联。