TY - JOUR
T1 - TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancers
AU - Lolas-Hamameh, Suhair
AU - Lieberman, Sari
AU - Sarahneh, Alaa
AU - Walsh, Tom
AU - Lee, Ming K.
AU - Gulsuner, Suleyman
AU - Rabie, Grace
AU - Beeri, Rachel
AU - Aburayyan, Amal
AU - Mandell, Jessica B.
AU - Fridman, Hila
AU - Lazer-Derbeko, Galit
AU - Klopstock, Tehila
AU - Freireich, Orit
AU - Lahad, Amnon
AU - King, Mary Claire
AU - Levy-Lahad, Ephrat
AU - Kanaan, Moien N.
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Oxford University Press. All rights reserved.
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Pathogenic TP53 germline variants cause young-onset breast cancer and other cancers of the Li-Fraumeni syndrome (LFS) spectrum, but the clinical consequences of partial-loss-of function TP53 variants are incompletely understood. In the consecutive cohort of Palestinian breast cancer patients of the Middle East Breast Cancer Study (MEBCS), breast cancer risk among TP53 p.R181C heterozygotes was 50% by age 50 years and 81% by age 80 years. In contrast, prevalence of pediatric cancers in the MEBCS was similar among first-degree relatives of TP53 p.R181C carriers (3/519 = 0.0058) and first-degree relatives of MEBCS patients with no pathogenic germline variant in any known breast cancer gene (7/1082 = 0.0065; odds ratio [OR] = 0.90, 95% confidence interval [CI] [0.23 to 3.49], Fisher P =. 90 [2-tailed]). This result suggests that in families harboring this TP53 allele, genetic testing in children is unwarranted, and screening children for LFS tumors is unnecessary. More generally, some TP53 missense alleles can predispose to very high risk of breast cancer without pleiotropic effects.
AB - Pathogenic TP53 germline variants cause young-onset breast cancer and other cancers of the Li-Fraumeni syndrome (LFS) spectrum, but the clinical consequences of partial-loss-of function TP53 variants are incompletely understood. In the consecutive cohort of Palestinian breast cancer patients of the Middle East Breast Cancer Study (MEBCS), breast cancer risk among TP53 p.R181C heterozygotes was 50% by age 50 years and 81% by age 80 years. In contrast, prevalence of pediatric cancers in the MEBCS was similar among first-degree relatives of TP53 p.R181C carriers (3/519 = 0.0058) and first-degree relatives of MEBCS patients with no pathogenic germline variant in any known breast cancer gene (7/1082 = 0.0065; odds ratio [OR] = 0.90, 95% confidence interval [CI] [0.23 to 3.49], Fisher P =. 90 [2-tailed]). This result suggests that in families harboring this TP53 allele, genetic testing in children is unwarranted, and screening children for LFS tumors is unnecessary. More generally, some TP53 missense alleles can predispose to very high risk of breast cancer without pleiotropic effects.
UR - http://www.scopus.com/inward/record.url?scp=105004681365&partnerID=8YFLogxK
U2 - 10.1093/jnci/djae334
DO - 10.1093/jnci/djae334
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C2 - 39673796
AN - SCOPUS:105004681365
SN - 0027-8874
VL - 117
SP - 1069
EP - 1073
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 5
ER -
