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. 2024 Jun 29;16(13):2411.
doi: 10.3390/cancers16132411.

Somatic Mutations in KEAP1-NRF2 Complex in Breast Cancer

Micaela Almeida  1   2   3 , Catarina L Ferreira  1   2 , Rosa Maria Tomé  2   4 , José Fonseca-Moutinho  1   2   4 , António Polónia  3   5 , Ana Cristina Ramalhinho  1   2   4 , Luiza Breitenfeld  1   2
Affiliations

Somatic Mutations in KEAP1-NRF2 Complex in Breast Cancer

Micaela Almeida et al. Cancers (Basel). .

Abstract

Breast cancer remains the leading cause of cancer deaths for women. Long-term estrogen exposure is considered carcinogenic due to semiquinone production and to compromised detoxification. Metabolic regulator polymorphisms, such as KEAP1 (rs1048290) and NRF2 (rs35652124, rs6721961, rs6706649), can be valuable in understanding the individual cytoprotection profile. Thus, we aim to genotype these polymorphisms in blood, tumours and surrounding tissue, to identify somatic mutations and correlate it to prognoses. A total of 23 controls and 69 women with histological confirmed breast cancer were recruited, and DNA from blood/surrounding/tumour tissue was genotyped. Genotyping and clinicopathological data were correlated. We verified that rs35652124 presents different genotype distribution between the blood/surrounding tissue (p-value = 0.023) and tumour/surrounding tissues (p-value = 0.041). Apart from rs35652124 and considering the histological grade, the other four polymorphisms have different distributions among different tissues. There is a tendency towards the loss of heterozygosity in the surrounding tissue when compared to blood and tumour tissues, and higher genotype variability in histologic grade 2. These somatic mutations and different distribution patterns may indicate a heterogeneous and active microenvironment, influencing breast cancer outcome. Additionally, it would be pertinent to evaluate the predictive value of the histologic grade 2 considering somatic mutation profiles and distributions.

Keywords: KEAP1; NRF2; breast cancer.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Number of acquired mutations in the surrounding and tumour tissues, when compared to the genotype profile of the blood.
See this image and copyright information in PMC

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