PALB2 Variants Extend the Mutational Profile of Hungarian Patients with Breast and Ovarian Cancer

Author:

Butz Henriett1234,Nagy Petra1,Papp János13,Bozsik Anikó13ORCID,Grolmusz Vince Kornél13,Pócza Tímea1,Oláh Edit1,Patócs Attila134ORCID

Affiliation:

1. Department of Molecular Genetics, The National Tumor Biology Laboratory, National Institute of Oncology, Comprehensive Cancer Center, 1122 Budapest, Hungary

2. Department of Oncology Biobank, National Institute of Oncology, 1122 Budapest, Hungary

3. Hereditary Tumours Research Group, Eötvös Loránd Research Network, 1089 Budapest, Hungary

4. Department of Laboratory Medicine, Semmelweis University, 1092 Budapest, Hungary

Abstract

Background: The pathogenic/likely pathogenic (P/LP) variant detection rate and profile of PALB2, the third most important breast cancer gene, may vary between different populations. Methods: PALB2 was analyzed in peripheral blood samples of three independent cohorts: prospectively between September 2021 and March 2023 (i) in 1280 consecutive patients with breast and/or ovarian cancer (HBOC), (ii) in 568 patients with other cancers (controls), and retrospectively, (iii) in 191 young breast cancer (<33 years, yBC) patients. These data were compared with data of 134,187 non-cancer individuals retrieved from the Genome Aggregation Database. Results: Altogether, 235 cases (235/1280; 18.3%) carried at least one P/LP variant in one of the HBOC susceptibility genes. P/LP PALB2 variants were identified in 18 patients (1.4%; 18/1280) in the HBOC and 3 cases (1.5%; 3/191) in the yBC group. In the control group, only one patient had a disease-causing PALB2 variant (0.17%; 1/568) as a secondary finding not related to the disease, which was similar (0.15%; 205/134,187) in the non-cancer control group. The NM_024675.4:c.509_510delGA variant was the most common among our patients (33%; 6/18). We did not find a significant difference in the incidence of PALB2 disease-causing variants according to age; however, the median age of tumor onset was lower in PALB2 P/LP carriers versus wild-type patients (44 vs. 48 years). In our cohort, the odds ratio for breast cancer risk in women with PALB2 P/LP variants was between 8.1 and 9.3 compared to non-HBOC cancer patients and the non-cancer population, respectively. Conclusions: PALB2 P/LP variants are not uncommon among breast and/or ovarian cancer patients. Their incidence was the same in the two breast cancer cohorts studied but may occur rarely in patients with non-breast/ovarian cancer. The c.509_510delGA variant is particularly common in the studied Hungarian patient population.

Funder

Hungarian Scientific Research

New National Excellence Program of the Ministry of Human Capacities

National Laboratories Excellence program (under the National Tumour Biology Laboratory project

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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