Molecular landscape of hereditary melanoma

JRMB Arnaut, I dos Santos Guimarães… - Critical Reviews in …, 2021 - Elsevier
Melanoma is considered the most lethal skin cancer and its incidence has increased during
the past decades. About 10% of cases are classified as hereditary melanoma. Genetic …

[HTML][HTML] Melanoma susceptibility: an update on genetic and epigenetic findings

OAH Truderung, JC Sagi, AF Semsei… - International Journal of …, 2021 - ncbi.nlm.nih.gov
Malignant melanoma is one of the most highly ranked cancers in terms of years of life lost.
Hereditary melanoma with its increased familial susceptibility is thought to affect up to 12 …

[HTML][HTML] Predictors of germline status for hereditary melanoma: 5 years of multi-gene panel testing within the Italian Melanoma Intergroup

W Bruno, B Dalmasso, M Barile, V Andreotti, L Elefanti… - ESMO open, 2022 - Elsevier
Background The incidence of cutaneous melanoma is increasing in Italy, in parallel with the
implementation of gene panels. Therefore, a revision of national genetic assessment criteria …

Integrative metagenomic, transcriptomic, and proteomic analysis reveal the microbiota-host interplay in early-stage lung adenocarcinoma among non-smokers

Y Sun, Z Gan, X Wang, J Liu, W Zhong, Z Zhang… - Journal of Translational …, 2024 - Springer
Background The incidence of early-stage lung adenocarcinoma (ES-LUAD) is steadily
increasing among non-smokers. Previous research has identified dysbiosis in the gut …

GOLM1: expanding our understanding of melanoma susceptibility

EJ Maas, CK Wallingford, E DeBortoli… - Journal of Medical …, 2023 - jmg.bmj.com
Altered GOLM1 expression is associated with tumorigenesis, but only one GOLM1 variant
(p. S307L), has ever been reported in association with disease (familial melanoma). 1 …

Insights into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1

L Pastorino, V Andreotti, B Dalmasso, I Vanni… - Cancers, 2020 - mdpi.com
The contribution of recently established or candidate susceptibility genes to melanoma
missing heritability has yet to be determined. Multigene panel testing could increase …

Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families

F Fidalgo, GT Torrezan, BCS Sá, BDF Barros… - PLoS …, 2022 - journals.plos.org
Genetic predisposition accounts for nearly 10% of all melanoma cases and has been
associated with a dozen moderate-to high-penetrance genes, including CDKN2A, CDK4 …

Knockdown of Golgi phosphoprotein 73 blocks the trafficking of matrix metalloproteinase‐2 in hepatocellular carcinoma cells and inhibits cell invasion

Y Liu, X Zhang, S Zhou, J Shi, Y Xu, J He… - Journal of cellular …, 2019 - Wiley Online Library
Abstract Golgi phosphoprotein 73 (GP 73) has been regarded as a novel serum biomarker
for the diagnosis of hepatocellular carcinoma (HCC) in recent years. It has been reported …

[HTML][HTML] Golgi protein 73, hepatocellular carcinoma and other types of cancers

Y Wang, YJY Wan - Liver research, 2020 - Elsevier
Hepatocellular carcinoma (HCC) is one of the most common malignant tumors with a low
survival rate. The identification of mechanisms underlying the development of HCC helps …

Evolution of approaches to identify melanoma missing heritability

B Dalmasso, P Ghiorzo - Expert review of molecular diagnostics, 2020 - Taylor & Francis
Introduction: Around 10% of melanoma patients have a positive family history of melanoma
and/or related cancers. Although a germline pathogenic variant in a high-risk gene can be …