Genetic studies in Latin America have expanded, but further efforts are needed to understand cancer susceptibility genes beyond BRCA1 and BRCA2, especially by characterizing the prevalence and spectrum of pathogenic or likely pathogenic variants (PVs) in the region. This study aimed to determine the frequency of hereditary cancer syndromes (HCS) in Colombians with solid tumors and to characterize the spectrum of PVs. Using data from the Colombia's largest Institutional Hereditary Cancer Program, we included patients aged ≥18 years with solid tumors who met HCS criteria and were offered genetic testing with a 105-cancer gene panel. We calculated the prevalence of PVs and HCS by cancer type (beyond breast) and gene. For patients with breast cancer, we examined genotype-phenotype correlations with molecular subtypes and stratified positivity rates by different genetic testing criteria. Among 769 patients, we identified 216 PVs in 43 genes in 197 patients (26%). Thirty-three PVs were recurrent. Autosomal HCS was found in 21% (160/769) of patients (159 dominant, one recessive), while 5% (37/769) were heterozygous carriers of PVs in autosomal recessive genes. In 42% (321/769) of the cases, only one or more variants of uncertain significance (VUS) were identified, whereas 33% (251/769) had neither PVs nor VUS detected (negative results). HCS prevalence varied by cancer type (11-26%). The triple-negative subtype and bilateral presentation were strong predictors of inherited breast cancer. Our study reveals a significant presence of PVs among high-risk Colombian patients with solid tumors, underscoring the importance of genetic counseling and testing in the region.
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http://dx.doi.org/10.1038/s41431-025-01807-y | DOI Listing |
Cureus
February 2025
Department of Breast Surgery, Osaka Rosai Hospital, Osaka, JPN.
and () mutation screening is recommended for patients with advanced breast cancer or early breast cancer suspected to have hereditary origins based on family history or tumor characteristics. Blood-based testing is the standard approach, but it is not feasible in patients who have undergone bone marrow transplantation due to the replacement of blood cells with donor-derived cells. We report a case of a patient who, following bone marrow transplantation, required an alternative to blood-based germline screening.
View Article and Find Full Text PDFEur J Hum Genet
March 2025
Office of Academic Diversity, Division of Diversity, Equity and Inclusion, University of California at Davis, Davis, CA, USA.
Genetic studies in Latin America have expanded, but further efforts are needed to understand cancer susceptibility genes beyond BRCA1 and BRCA2, especially by characterizing the prevalence and spectrum of pathogenic or likely pathogenic variants (PVs) in the region. This study aimed to determine the frequency of hereditary cancer syndromes (HCS) in Colombians with solid tumors and to characterize the spectrum of PVs. Using data from the Colombia's largest Institutional Hereditary Cancer Program, we included patients aged ≥18 years with solid tumors who met HCS criteria and were offered genetic testing with a 105-cancer gene panel.
View Article and Find Full Text PDFNaunyn Schmiedebergs Arch Pharmacol
March 2025
Medical Laboratory Technique College, the Islamic University, Najaf, Iraq.
Gastric cancer (GC) is the result of a convoluted series of incidents that include host genetic susceptibility, Helicobacter pylori infection, and other external influences. The emergence of many hereditary and chromatin modifications in carcinogenic and tumor-inhibiting genes results in the disruption of several molecular networks, upsetting the balance between cell proliferation and apoptosis as well as the cell cycle. Important roles are played by members of the Toll-like receptor (TLR) family in both native and adaptive immunological reactions.
View Article and Find Full Text PDFNeurosurg Rev
March 2025
Department of Neurosurgery, Allegheny Health Network Neuroscience Institute, Pittsburgh, PA, US.
Li-Fraumeni Syndrome (LFS) is a rare hereditary cancer syndrome characterized by an increased risk of early-onset and multiple tumors across various organ systems, predominantly linked to germline TP53 mutations. While commonly associated neoplasms include sarcomas, breast cancer, and adrenocortical carcinoma, the occurrence of high-grade gliomas (HGG), including glioblastoma multiforme (GBM), in LFS patients is less documented and typically presents at a younger age relative to sporadic cases. A systematic review following PRISMA guidelines was conducted, focusing on clinical studies and case reports that explore the association between HGG and LFS.
View Article and Find Full Text PDFJID Innov
May 2025
Department of Dermatology, Alfred Health, Melbourne, Australia.
Dystrophic epidermolysis bullosa (DEB) is a hereditary skin fragility disease characterized by the loss or dysfunction of collagen VII, predisposing patients to dermal-epidermal separation. This disease is highly associated with the development of progressive fibrosis of the skin and other organs and the occurrence of lethal cutaneous squamous cell carcinomas (cSCCs). These are not only caused by chronic wounding but also by collagen VII deficiency, which may directly alter cellular responses.
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