# Beyond the BRCA1/2 genes in ovarian cancer: the role of germline pathogenic variants in the ATM gene

**Authors:** Daniele Guadagnolo, Angelo Minucci, Antonella Chiavassa, Gabriella Gentile, Francesca Salvatori, Nader Khaleghi Hashemian, Giulia Maneri, Maria Piane, Simona Grotta, Paola Grammatico, Antonio Pizzuti, Daniele Santini, Laura De Marchis

PMC · DOI: 10.1007/s11033-025-10357-x · Molecular Biology Reports · 2025-02-21

## TL;DR

This paper discusses how ATM gene mutations can increase ovarian cancer risk and highlights the need for better guidelines for managing such cases.

## Contribution

The study presents two cases of ovarian cancer linked to ATM gene mutations, emphasizing their role in cancer predisposition.

## Key findings

- Germline heterozygous pathogenic variants in the ATM gene are associated with increased ovarian cancer risk.
- Current guidelines lack clear evidence on the benefits of prophylactic surgery for ATM mutation carriers.
- ATM mutations should be considered in ovarian cancer prevention strategies alongside BRCA1/2.

## Abstract

Ovarian Cancer (OC) prevention and early-stage detection represents a challenge due to the lack of effective surveillance. The identification of high-risk women is crucial as it provides access to prophylactic oophorectomy and reduces disease burden. Next-Generation Sequencing approaches enable the investigation of several genes associated with monogenic hereditary cancer predisposition, including ovarian cancer. For family members of patients affected by ovarian cancer without identification of a germline pathogenic variant, despite the increased empirical risk (3 times) of ovarian cancer incidence, prophylactic surgery is not indicated but may be suggested as the only efficient strategy.

We hereby present 2 cases of OC in which a germline heterozygous pathogenic variant in the ATM gene was identified: the first in the contest of Hereditary Breast and Ovarian Cancer (HBOC) family history and, in the other one, a late onset of neoplasms, to underline the importance of defining guidelines and management of moderate penetrance genes variants also for ovarian cancer prevention.

Carriers of heterozygous pathogenic variants in the ATM gene have an increased risk of neoplasms incidence, mostly breast but also of OC with an absolute estimated risk of 2–3 times greater than the general population. For these patients there is not well-established evidence of benefit in risk reducing bilateral Salpingo-oophorectomy.

## Linked entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672], BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675], ATM (ATM serine/threonine kinase) [NCBI Gene 472]
- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** ATM (ATM serine/threonine kinase) [NCBI Gene 472] {aka AT1, ATA, ATC, ATD, ATDC, ATE}
- **Diseases:** neoplasms (MESH:D009369), OC (MESH:D010051), HBOC (MESH:D061325), hereditary cancer (MESH:D009386)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC11845405/full.md

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Source: https://tomesphere.com/paper/PMC11845405