共 138 条
Cancer and Tumour Suppressor p53 Encounters at the Juncture of Sex Disparity
被引:12
作者:

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Haupt, Ygal
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Peter MacCallum Canc Ctr, Tumor Suppress Lab, Melbourne, Vic, Australia
Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic, Australia
Univ Melbourne, Dept Clin Pathol, Parkville, Vic, Australia
Monash Univ, Dept Biochem & Mol Biol, Melbourne, Vic, Australia Peter MacCallum Canc Ctr, Tumor Suppress Lab, Melbourne, Vic, Australia
机构:
[1] Peter MacCallum Canc Ctr, Tumor Suppress Lab, Melbourne, Vic, Australia
[2] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic, Australia
[3] Univ Melbourne, Dept Clin Pathol, Parkville, Vic, Australia
[4] Monash Univ, Dept Biochem & Mol Biol, Melbourne, Vic, Australia
关键词:
p53;
sex disparity;
cancer;
oxidative stress;
SNPs;
epigenetics;
post translational modifications;
non-coding RNAs;
D O I:
10.3389/fgene.2021.632719
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
There are many differences in cancer manifestation between men and women. New understanding of the origin of these point to fundamental distinctions in the genetic code and its demise. Tumour suppressor protein p53 is the chief operating officer of cancer defence and critically acts to safeguard against sustained DNA damaged. P53 cannot be ignored in cancer sex disparity. In this review we discuss the greater prevalence and associated death rates for non-reproductive cancers in males. The major tumour suppressor protein p53, encoded in the TP53 gene is our chosen context. It is fitting to ask why somatic TP53 mutation incidence is estimated to be disproportionately higher among males in the population for these types of cancers compared with females? We scrutinised the literature for evidence of predisposing genetic and epigenetic alterations that may explain this sex bias. Our second approach was to explore whether redox activity, either externally imposed or inherent to males and females, may define distinct risks that could contribute to the clear cancer sex disparities.
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