Emergence of BRCA Reversion Mutations in Prostate Cancer Prior to PARP Inhibitor Exposure: Clinical and Therapeutic

Douglas I Lin1, Elizabeth Lawrence1, Natalie Danziger1

  • 1Foundation Medicine, Inc., Boston, Massachusetts, USA.

Cancer Medicine
|January 15, 2026
PubMed
Abstract

Insights

BRCA reversion mutations can emerge in prostate cancer patients even without prior PARPi therapy, especially after chemotherapy and radiation. This suggests DNA-damaging treatments may drive resistance to PARPi drugs.

Area of Science:

  • Oncology
  • Genetics
  • Pharmacology

Background:

  • Inactivating BRCA1/2 mutations predict poly(ADP-ribose) polymerase inhibitor (PARPi) sensitivity in prostate cancer (PCA).
  • Secondary BRCA1/2 reversion mutations (BRCArev) can restore BRCA function, leading to acquired PARPi resistance.
  • The emergence of BRCArev in PARPi-naïve settings is not well understood.

Purpose of the Study:

  • To investigate the frequency and clinical context of BRCArev detection in advanced prostate cancer patients.
  • To explore therapeutic correlates of BRCArev, including in patients without prior PARPi exposure.

Main Methods:

  • Retrospective analysis of liquid biopsy results (FoundationOneLiquid CDx) from PCA patients (Jan-Dec 2023).
  • Definition of BRCArev as alterations restoring BRCA1/2 open reading frame in patients with pathogenic variants.
  • Abstraction of clinical and treatment histories, including chemotherapy and PARPi exposure.

Main Results:

  • BRCArev were identified in 30% (3/10) of PARPi-naïve PCA patients with BRCA1/2 alterations.
  • These PARPi-naïve patients had prior chemotherapy (platinum/docetaxel) and radiation, with multiple BRCArev events.
  • Patients with prior olaparib exposure (7/10) showed varied response durations based on prior chemotherapy status.

Conclusions:

  • BRCArev can arise in prostate cancer without prior PARPi therapy, particularly after DNA-damaging treatments like chemotherapy and radiation.
  • These findings suggest that DNA-damaging therapies may promote BRCArev formation, potentially causing primary PARPi resistance.
  • Early PARPi therapy before chemotherapy could improve clinical benefit and prevent primary resistance.

Related Concept Videos

The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.7K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
6.3K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
8.6K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
4.6K