Ovarian cancer accounts for 2.5% of all malignancies among women but accounts for 5% of total female cancer deaths (Torre et al., 2018). Due to general and non-specific symptoms of the early disease and the lack of early detection screening options, patients usually present with advanced disease at the time of diagnosis. Approximately 18% of epithelial ovarian cancer cases, particularly high-grade serous carcinomas, are due to inherited mutations in BRCA1/2 genes; these mutations account for almost 40% of ovarian cancer cases in women with a family history of the disease (Couch et al., 2014). Currently, the FDA has approved olaparib, niraparib, and rucaparib for treating and managing BRCA-mutated ovarian cancers. In December 2014, the FDA approved the first PARP inhibitor, olaparib, as a monotherapy for patients with advanced BRCA1/2-mutated ovarian cancer who were treated with three or more prior lines of chemotherapy based on the promising results from a Phase II clinical trial (NCT0107662) (Kaufman et al., 2015; Arora et al., 2021). The FDA then expedited the approval of rucaparib and niraparib based on the ARIEL2 and Study 10 clinical trials for rucaparib and the QUADRA clinical trial for niraparib (Oza et al., 2017; Moore et al., 2019). Rucaparib was approved for advanced BRCA1/2 mutated ovarian carcinomas following multiple chemotherapy treatments, while niraparib was approved for homologous recombination deficiency (HRD)-positive gynecological cancers (Franzese et al., 2019; Kim and Nam, 2022). Following the initial approvals, Phase III clinical trials continued to demonstrate the efficacy of PARP inhibitors in gynecological cancers.

The SOLO2 clinical trial was a Phase III, double-blinded, randomized, placebo-controlled study that evaluated the use of olaparib as maintenance therapy in platinum-sensitive, relapsed ovarian cancer patients with a BRCA1/2 mutation who had received at least two lines of previous chemotherapy (Pujade-Lauraine et al., 2017). After at least 4 cycles of platinum-based treatment, 196 of 295 patients were randomly assigned to receive either 300 mg of olaparib twice daily in tablet form or a placebo. In the trial group, 67% of these patients had confirmed germline BRCA1 mutations, while 30% had BRCA2 mutations and the remaining patients had missing information regarding their mutation status. The olaparib group’s median progression-free survival (PFS) was 19.1 months, compared to 5.5 months in the control group. The trial also found that olaparib had manageable toxicities and no detrimental effects on the quality of life in these patients. This trial eventually led to the approval of olaparib for BRCA1/2-mutated ovarian cancer patients with at least two lines of previous chemotherapy (Franzese et al., 2019).

The SOLO1 trial was also a Phase III, double-blinded, randomized study that evaluated the use of olaparib as maintenance therapy for patients with newly diagnosed high-grade serous or endometrioid ovarian cancer, primary peritoneal cancer, or fallopian tube cancer (or a combination thereof) with BRCA1/2 mutations who had responded to first time platinum-based chemotherapy (Moore et al., 2018; DiSilvestro et al., 2022). In the initial trial, of the 391 enrolled patients, 260 were randomly assigned to receive 300 mg of olaparib twice daily, while the remaining 131 received a placebo (Moore et al., 2018). Median PFS for patients receiving a placebo was 13.8 months; meanwhile for those receiving olaparib was 56.0 months. This trial eventually led to the approval of olaparib for this indication. A 7-year follow-up of these patients further support the use of olaparib to slow down the remission for this indication (DiSilvestro et al., 2022).

The ENGOT-OV16/NOVA Phase III clinical trial was a randomized, double-blinded, placebo-controlled study of niraparib as maintenance in platinum-sensitive ovarian cancer patients with either germline BRCA (gBRCA) mutation or a tumor with high-grade serous histology who have responded to their most recent chemotherapy containing a platinum agent (Mirza et al., 2016). For this review, we will focus on the gBRCA cohort, which contained 203 patients, 138 of whom were in the niraparib group and were given 300 mg of niraparib daily instead of a placebo. Of the treatment group, 61.6% had BRCA1 mutations, 37.0% had BRCA2 mutations, and 6.5% had either BRCA1 or BRCA2 rearrangements, or both. In the gBRCA cohort, the median PFS was 21.0 months compared to 5.5 months in the placebo group. The most common severe adverse effects of niraparib were thrombocytopenia, anemia, and neutropenia, controlled with dose modification (Mirza et al., 2016; Berek et al., 2018). The results of this trial played a crucial role in the FDA approval of niraparib for the maintenance therapy of adult patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in complete or partial remission following platinum-based chemotherapy (Franzese et al., 2019).

The ARIEL3 Phase III clinical trial was a randomized, double-blind, placebo-controlled trial that evaluated the efficacy of rucaparib as a maintenance therapy for women with platinum-sensitive ovarian cancer who had achieved a complete or partial response to second-line or later platinum-based chemotherapy (Coleman et al., 2017). This trial had multiple cohorts, but for the purpose of this review, we will focus on the BRCA1/2-mutant cohort. Out of 196 patients randomized in this group, 130 were given a daily regimen of rucaparib 600 mg twice daily, while the remainder received a placebo. The treatment group of the gBRCA1/2 cohort comprised 61.5% BRCA1 mutants and 38.0% BRCA2 mutants. The median progression-free survival was significantly longer in the rucaparib group at 16.6 months compared to 5.4 months in the placebo group. This trial was pivotal in granting rucaparib FDA approval in 2018 for maintenance therapy of recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancers in complete or partial remission to platinum-based chemotherapies.

The ARIEL4 Phase III clinical trial was a randomized, controlled, open-label study that sought to evaluate the efficacy of rucaparib as an alternative treatment option to chemotherapy for patients with relapsed, BRCA1/2-mutated ovarian cancers (Kristeleit et al., 2022). Among the multiple cohorts included in this trial, the present review focuses on the efficacy population, which excluded patients with BRCA1/2 reversion mutations. Of the 325 patients in the efficacy group, 220 received oral rucaparib 600 mg twice daily in 28-day cycles, regardless of platinum sensitivity status. The treatment group consisted of 79% BRCA1 mutants and 21% BRCA2 mutants. The median progression-free survival was significantly longer in the rucaparib group at 7.4 months compared to 5.4 months in the placebo group. Overall, the results of the ARIEL4 study support the use of rucaparib as a viable alternative to chemotherapy for patients with relapsed, BRCA1/2-mutated ovarian carcinoma.

Breast cancer is the second most common cancer in the world (Ferlay et al., 2019), which has a wide range of risk factors that include but are not limited to family history, age, and environmental factors (Collaborative Group on Hormonal Factors in Breast, 2001; Cortesi et al., 2021). Approximately 5–10% of patients diagnosed with breast cancer have an inherited loss of function in one or both BRCA1 and BRCA2 genes (Couch et al., 2014). FDA has approved two PARP inhibitors, olaparib and talazoparib, for therapeutic use in breast cancers with germline and somatic BRCA1/2 mutations.

The OlympiAD clinical trial was a Phase III, open-labeled, randomized, multicenter, international study that evaluated the use of olaparib as monotherapy for the treatment of HER2-negative metastatic breast cancer with germline BRCA1/2 mutations (Robson et al., 2017; Robson et al., 2019). Of the 302 enrolled patients, 205 were randomly assigned to receive 300 mg of olaparib twice daily, while the remaining 97 received standard therapy (capecitabine, eribulin, or vinorelbine). In the trial group, BRCA1 germline mutations were present in 57.1% of the patients, BRCA2 mutations were present in 41.0% of the patients, and 2% of the patients carried mutations in both genes. The trial included participants who received less than two prior chemotherapy regimens for metastatic disease. Participants were selected because they had received neoadjuvant, adjuvant, or treatment for metastatic disease with an anthracycline (unless contraindicated) and a taxane. Patients were excluded if the disease relapsed within 12 months of adjuvant platinum. In the trial, olaparib outperformed standard therapy regarding median PFS time and toxicity. PFS was 7.0 months in the trial group and 4.2 months in the standard therapy. The risk of disease progression or death was 42% lower with olaparib monotherapy than with standard therapy. Olaparib also had fewer grade 3 or higher adverse events.

The OlympiA double-blinded, randomized Phase III trial was performed to determine if olaparib could reduce the rate of recurrence of cancers in individuals with BRCA1/2 mutations (Tutt et al., 2021). The 1836 individuals were randomly assigned to receive olaparib maintenance for a year or a placebo. In these patients, BRCA1 germline mutations were present in 71.3% of the patients, BRCA2 mutations were present in 28.3% of the patients, and 0.2% of patients carried mutations in both genes. Olaparib outperformed the standard therapy and was associated with significantly longer invasive disease-free survival (IDFS) and distant disease-free survival (DDFS) than the standard therapy. Specifically, 3-year DDFS was 7.1% greater in the olaparib group compared to the placebo group, while 3-year IDFS was 8.8% greater in the olaparib group. In addition, fewer deaths were reported in the olaparib group. This trial determined that olaparib could be used as maintenance therapy for early breast cancer patients who are HER2-negative and have BRCA1/2 germline mutations. Follow-ups from the OlympiA clinical trial demonstrated a statistically significant improvement in overall survival with olaparib treatment, with an absolute improvement in 4-year overall survival of 3.4%, with 89.8% of patients in the olaparib group surviving compared to 86.4% in the placebo group. The participants maintained improvements in IDFS and DDFS (Geyer et al., 2022). This trial led to the approval of olaparib as a maintenance therapy for BRCA1/2 mutated breast cancers.

The Phase III EMBRACA trial was a randomized, open-label trial that led to the FDA approval of talazoparib for breast cancer patients (Litton et al., 2018; Litton et al., 2020). Talazoparib monotherapy was used in this trial to treat HER2-negative metastatic breast cancers with germline BRCA1/2 mutation. In this trial, 287 out of 431 participants were given 1 mg talazoparib once daily, and the rest of the patients were given standard therapy. In the talazoparib group, BRCA1 germline mutations were present in 46.3% of the patients and BRCA2 mutations were present in 53.7% of the patients. Participants were selected if they had received no more than three previous cytotoxic regimens for advanced breast cancer. They received prior treatment with a taxane, an anthracycline, or both unless this treatment was contraindicated. Patients were excluded if they had objective disease progression while receiving platinum chemotherapy for advanced breast cancer. The median PFS among patients in the talazoparib group was approximately 2.8 months longer than in the standard therapy group, with a median PFS of 7.0 months in the talazoparib group and 4.2 months in the standard therapy group.

Prostate cancer is the most common cancer and the second leading cause of cancer death in men in the United States. The incidence of prostate cancer varies widely among different populations. In general, the rates of prostate cancer are the highest in North America and Europe and lowest in Asia and Africa (Pernar et al., 2018). The exact reason for these differences is not well understood but is likely due to a combination of genetic, environmental, and lifestyle factors. Of the inherited prostate cancers, approximately 5.3% contain BRCA2 and 0.9% contain BRCA1 mutations making these subsets of prostate cancer ideal targets for PARP inhibitor therapy (Messina et al., 2020). In May 2020, the FDA granted accelerated approval for rucaparib based on the TRITON2 Phase II trial for the treatment of adult patients with metastatic castrate-resistant prostate cancer (mCRPC) associated with a deleterious BRCA mutation (germline and/or somatic) who have received androgen receptor-directed therapy and a taxane (Abida et al., 2020; Anscher et al., 2021). Olaparib also received approval based on the results of the Phase III PROfound trial (de Bono et al., 2020).

After the Phase III PROfound trial, olaparib monotherapy was approved for use in patients with mCRPC who have progressed after receiving prior treatment with enzalutamide or abiraterone and have detrimental germline or somatic homologous recombination repair (HRR) gene mutations (de Bono et al., 2020). This trial examined multiple HRR genes and looked closely at BRCA1, BRCA2, and ATM mutations in cohort A of this study. In cohort A, 162 patients were randomly assigned to receive olaparib and 83 to the control treatment. BRCA1 germline mutations were present in 5% of the patients, BRCA2 mutations were present in 49% of the patients, and 37% had ATM mutations. The remaining patients had a combination of the three mutations. For patients in cohort A, the median duration of follow-up via imaging-based PFS was 7.5 months in the olaparib group and 5.4 months in the control group. The study found that the median overall survival for cohort A was 18.5 months in the group receiving olaparib treatment, while it was 15.1 months in the control group. Exploratory analyses of this trial suggested that patients with BRCA1 or BRCA2 alterations derived the most benefit.

Pancreatic cancer is a relatively rare but aggressive form of cancer, and it is often difficult to diagnose in its early stages. The outlook for pancreatic cancer depends on the cancer stage at the time of diagnosis, but it is generally considered a very serious and difficult-to-treat cancer with a 5-year survival of approximately 9%. BRCA1/2 mutations have been identified in familial pancreatic cancers, with the majority being germline BRCA2 gene mutations, which occur in approximately 5–17% of patients with familial pancreatic cancer (Rawla et al., 2019). As a result, this subset of pancreatic cancers is a prime target for treatment with PARP inhibitors.

Currently, the only FDA-approved PARP inhibitor to treat pancreatic cancers is olaparib. The approval is based on the POLO Phase III clinical trial that was randomized, double-blind, and placebo controlled (Golan et al., 2019). In this study, 92 patients out of 154 participants were given olaparib (300 mg, twice daily), while the remainder were given a placebo. In these patients, BRCA1 germline mutations were present in 32% of the patients, BRCA2 mutations were present in 67% of the patients, and 1% of the patients carried mutations in both genes. After 2 years, olaparib treatment prevented tumor development in 22.1% of patients with chemotherapy-responsive BRCA1/2-mutated malignancies. In comparison, only 9.6% of individuals receiving the placebo had no tumor development. In addition, the median PFS was 7.4 and 3.8 months after treatments with olaparib and the control medication, respectively. Overall, the POLO trial showed that maintenance olaparib provided significant benefits to patients with a BRCA1/2 mutation and metastatic pancreatic cancer that had not progressed during platinum-based chemotherapy (Golan et al., 2019; Kindler et al., 2022).

PARP inhibitors have shown promising results in treating cancers that have genetic defects in homologous recombination repair (HRR), particularly those related to BRCA mutations. To determine which patients are most likely to respond to these therapies, various genetic tests have been developed to identify variant, deletion, or duplication mutations in the BRCA1 and BRCA2 genes (Toland et al., 2018). Several of the trials discussed in the previous section rely on the Homologous Recombination Deficiency (HRD) tests, which assess the degree of HRD in cancer cells by the presence of genomic scars (Ngoi and Tan, 2021). During phase III clinical trials, patient selection was based on the presence of BRCA mutations, and different testing methods were used based on availability. The FoundationOne CDx next-generation sequencing test and the BRACAnalysis CDx Germline Companion Diagnostic Test were used in some trials, and both have been FDA-approved as companion tests to match patients with specific PARP inhibitor drugs. An in-depth review of these techniques to detect BRCA-mutations was recently described by Concolino, P. & Capoluongo (Concolino and Capoluongo, 2019).

The BRACAnalysis CDx was first approved by the FDA in conjunction with the PARP inhibitor Olaparib, specifically for the selection of BRCA mutations in ovarian cancer patients. This diagnostic tool is designed to detect and classify variants in the germline BRCA1 and BRCA2 genes, including single nucleotide variants (SNVs) and small insertions or deletions, through PCR and Sanger sequencing. The BRACAnalysis CDx also includes an extensive rearrangement test, known as BART CDx, which detects major genomic rearrangements using multiplex PCR. The complete sequence analysis of the BRCA1 and BRCA2 genes is carried out using the BRACAnalysis CDx by evaluating approximately 5400 and 10,200 base pairs, respectively. This test examines the coding and non-coding regions of the BRCA1 and BRCA2 genes (Gunderson and Moore, 2015). The second FDA-approved companion test for determining eligibility for PARP inhibitors is the FoundationOne CDx next-generation sequencing test. This test utilizes the Next Generation Sequencing (NGS)-based comprehensive genomic profiling technology to analyze 324 cancer genes in solid tumors, including BRCA. The FoundationOne CDx reports known and likely pathogenic short variants, copy number alterations, select rearrangements, as well as complex biomarkers such as tumor mutational burden, microsatellite instability, and genomic loss of heterozygosity in ovarian cancer (Milbury et al., 2022). These tests can be used for a multitude of cancers, making them a crucial tool. A comprehensive list of FDA-approved companion tests and their approved use can be seen at the following link: https://www.fda.gov/medical-devices/in-vitro-diagnostics/list-cleared-or-approved-companion-diagnostic-devices-in-vitro-and-imaging-tools. Given the complex nature of repair defects and the multitude of proteins involved, it is not surprising that there is still no established gold standard for HRD-deficiency detection (Ngoi and Tan, 2021). Consequently, there is a pressing need to develop more reliable diagnostic technology to test for the underlying genomic signatures associated with successful use of PARP inhibition.

One of the well characterized DTR loci that frequently poses challenges to the replisome is the telomere. Mammalian telomeres consist of tandem repetitive DNA sequences, (TTAGGG)_n, located at the end of each linear chromosome. The length of human telomeres varies from 10 to 15 kb (Blasco, 2005). The enzyme telomerase catalyzes the de novo synthesis of TTAGGG at the shortened telomeres. Telomerase is a large ribonucleoprotein (RNP) complex and it elongates telomeres by copying its RNA component, hTR, with its intrinsic reverse transcriptase activity. 85–90% of cancers manifest robust telomerase activity (TEL+) (Kim et al., 1994; Shay and Bacchetti, 1997). However, in 10–15% of cancers, the telomerase activity is undetectable yet these cancer cells still can elongate their telomeres. These cancers adopt the so-called Alternative Lengthening of Telomere (ALT) pathway to maintain their telomeres (Bryan et al., 1995; Bryan et al., 1997).

The unique sequence and structural features of human telomeres render them especially challenging to replisomes (Figure 1A and Table 3). (1) One of the strands of telomere is rich in guanines (G) (thus called the G-rich strand) and is prone to form G4s (Biffi et al., 2013; Lam et al., 2013). (2) The subtelomeric/telomeric long non-coding RNA, TERRA, has been shown to form R-loops with telomeric DNA (Azzalin et al., 2007; Schoeftner and Blasco, 2008). (3) It was shown by Drosopoulos and colleagues that DNA replication can be initiated within telomeres; however, the large majority of DNA replication near the end of mammalian chromosomes is initiated from subtelomeres (Drosopoulos et al., 2012), suggesting that most telomeres lack DNA replication origins. Furthermore, Sfeir and colleagues showed that treatment with a low dosage of aphidicolin, a reversible DNA polymerase inhibitor, dramatically increases the incidence of fragile (broken) telomeres (Sfeir et al., 2009). These observations indicate that telomeres may be a special type of CFS. Furthermore, telomeres in the ALT-positive (ALT+) cells are more heterogeneous in length and some of them can be quite long (Bryan et al., 1995; Bryan et al., 1997). Therefore, ALT+ telomeres may be even more prone to express the fragility. (4) Heterochromatins are enriched at subtelomeres and telomeres (Blasco, 2007). (5) In order to protect the end of linear chromosomes, there are various high order DNA-DNA and DNA-protein structures at telomeres. For example, the telomeric G-rich strand overhang folds back, invades the internal double-stranded regions of telomeres, and forms the telomeric-loop (T-loop) as well as the displacement-loop (D-loop) (Griffith et al., 1999; Doksani et al., 2013). The T-loop and D-loop are further stabilized by the Shelterin complex and other proteins (de Lange, 2005; Pfeiffer and Lingner, 2013). These various high-order DNA-DNA and DNA-protein structures also slow down the replisome. Taken together, telomeres pose much greater challenges to the replisome than other regions of the human genome. Indeed, replication stress and spontaneous DNA damages are frequently detected at telomeres, especially in ALT+ cells (Cesare et al., 2009; Sfeir et al., 2009; Suram et al., 2012).

BRCA1 associates with telomeres in both TEL+ (Ballal et al., 2009) and ALT+ cells (Wu et al., 2003). Intriguingly, BRCA1 is recruited in higher amounts to ALT telomeres that experience heightened replication stress (Conomos et al., 2014; Pan et al., 2017). Mechanistically, our lab has shown that in coordination with BLM and FANCM, BRCA1 suppresses the TERRA R-loop accumulation-induced replication stress at the ALT telomeres and is required for the survival of ALT+ cancer cells (Pan et al., 2017). Moreover, Vohhodina and colleagues showed that BRCA1 directly binds TERRA RNA and also suppresses its expression in the ALT+ cancer cells (Vohhodina et al., 2021).

BRCA2 has also been shown to be implicated in DNA metabolism at telomeres. For example, BRCA2 facilities telomere synthesis/replication in TEL+ HeLa cells (Min et al., 2012). Moreover, it was also shown to facilitate the recruitment of Rad51, a key factor in HR, to telomeres in a unique HeLa derived clone, HeLa 1.2.11, which has super long telomeres (van Steensel et al., 1998; Badie et al., 2010). In mouse embryonic fibroblast (MEF) cells, deficiency of BRCA2 induces telomere fragility and telomere shortening (Badie et al., 2010; Min et al., 2012). Interestingly, Kwon and colleagues showed that BRCA2 deficiency facilitates the activation of the ALT pathway in telomerase-null mouse cells (Kwon et al., 2019). Consistent with these findings, we showed that BRCA2 is required for the formation of C-circles, an important ALT biomarker, in ALT+ cells that experience severe replication stress at their telomeres (Pan et al., 2019). Most intriguingly, Lee and colleagues demonstrated recently that BRCA2 directly binds the telomeric G4s in vitro, suggesting that it may be involved in disrupting the G4 accumulation, thereby preventing replication fork stalling at telomeres (Lee et al., 2022).

PARP1 plays a crucial role in maintaining the integrity of telomeres (Muoio et al., 2022). PARP1 can also be found at telomeres in both unstressed and IR- and H₂O₂-treated HeLa 1.2.11 (Gomez et al., 2006). In addition, PARP1 also associates with and PARylates TRF2 in vivo, a key component of the Shelterin complex. Interestingly, when Shelterin is removed, the repair of telomeric DNA damage requires the PARP1-dependent alternative non-homologous end joining pathway (alt-NHEJ) when the canonical NHEJ (cNHEJ) pathway is not available (Sfeir and de Lange, 2012). Furthermore, PARP1-dependent alt-NHEJ also contribute to the repair of telomere-internal DSBs induced by the endonuclease, Fok I (Doksani and de Lange, 2016). Finally, a recent study showed that PARP1 modulates the biogenesis and activity of telomerase through two RNA-binding proteins, DKC1 and GAR1(Savelyev et al., 2021).

Taken together, we propose that in BRCA1/2 deficient tumors, telomeres are more prone to unresolved replication stress and subsequent DNA damage. When these tumors are treated with PARPi, the combination of abrogated PARP1 catalytic activity-mediated events and the dramatic increase in trapped PARP1-PARPi DNA complexes leads to further blockage of replisome progression. This exacerbates the replication stress at telomeres and eventually kills the BRCA1/2 deficient cells.

Common fragile sites (CFSs) are identified as genomic regions that are prone to manifest ssDNA gaps in the metaphase spread assay when treated with low concentrations of aphidicolin, which slows but does not completely inhibit DNA replication (Glover et al., 1984; Hecht and Glover, 1984). The prominent features of CFSs include (Figure 1B and Table 3) (Glover et al., 2017): (1) enriching in deoxyadenosine and thymidine (AT-rich), which are prone to form hairpin DNA secondary structures; (2) enriching in long genes up to ∼5Mb; the transcription of the long genes could lead to formation of R-loops; (3) replicating late; and (4) lacking of replication origins.

In both pathogenic BRCA1 mutant cancer cells and BRCA1 siRNA depleted cancer cells, Arlt and colleagues showed that two CFSs, FRA3B and FRA16D, manifested elevated expression of the fragility compared to wild-type BRCA1 complemented or control siRNA transfected cells (Arlt et al., 2004). Consistent with these findings, Turner and colleagues reported that the loss of expression of Fhit, encoded by the long gene FHIT at the common fragile site, FRA3B, was more frequent in the BRCA1 mutant breast cancers than the sporadic breast cancers (Turner et al., 2002). They further showed that the BRCA1 deficient mouse cells also manifest more breaks and gaps at multiple CFSs. Similarly, Berthorsson and colleagues observed higher levels of genetic aberrations and allelic imbalance at FRA3B in the BRCA2 mutated hereditary breast cancers than in the sporadic breast cancers (Bergthorsson et al., 1998).

Using the metaphase spread assay, Vernole and colleagues did not observe any increased DNA breaks and gaps in the mismatch repair (MMR)-deficient colorectal cancers when PAPR1 was inactivated either with PARPi or siRNA when compared to the MMR-proficient colorectal cancers (Vernole et al., 2011). Similarly, using the spectral karyotyping technique, Lavoie and colleagues did not observe elevated expression of fragility in PARP1-null mouse cells either (Lavoie et al., 2005). However, using the recently developed Strand-seq technology, which can map genome-wide sister chromatid exchange (SCE) via single-cell sequencing, Heijink and colleagues showed that PARPi-induced SCEs frequently take place at many CFSs (Heijink et al., 2022). Notably, they demonstrated that these SCE events are independent of BRCA1 and BRCA2, suggesting that PARP1 likely acts in a parallel pathway facilitating the repair of replication blockage at the CFSs.

Collectively, strong evidence indicates that BRCA1, BRCA2, and PARP1 are all implicated in preventing replication stress and facilitating the repair/re-start of stalled replication forks at the CFSs. PARP1 likely functions in a parallel pathway of BRCA1 and BRCA2 in these molecular processes. Therefore, inhibition of PARP1 would further exacerbate the replication stress at the CFSs in the BRCA1/2 deficient tumors.

Centromeres are essential chromosome regions where kinetochores are assembled during mitosis and meiosis to ensure the equal partition of chromosomes (Barra and Fachinetti, 2018). However, because of the highly enriched various repetitive sequences, the identification of the exact sequences in the centromeric regions has been challenging for the short-read based sequencing technologies, such as Sanger sequencing and Next-Generation Sequencing (NGS). With the recently developed long-read sequencing technologies, such as Oxford Nanopore Technology (ONT), more precise sequence identification of the centromeric regions has been allowed. Two excellent review articles discussed how the exciting new telomere-to-telomere (T2T) human genome data would have a profound impact on the centromere research (Miga, 2020; Miga and Alexandrov, 2021). In general, there are a few prominent sequence features of the centromeric regions in humans (Figure 1C and Table 3): (1) enriching of various DNA repeats, including the alpha satellite repeats and long interspersed nuclear elements (LINEs); (2) spanning over several megabases long; (3) enriching of heterochromatin; (4) enriching of secondary DNA structures.

BRCA1 can be found at centrosomes throughout the cell cycle (Pageau and Lawrence, 2006; Zhu et al., 2011; Di Paolo et al., 2014). Intriguingly, Racca and colleagues showed that the formation of R-loops at the centromeric alpha satellite repeats further facilitates the association of BRCA1 with centromeres (Racca et al., 2021). Centromeric BRCA1 helps to prevent the accumulation of the centromeric alpha satellite R-loops formation (Racca et al., 2021). Consistent with these studies, Yilamz and colleagues showed that in G1 cells, DSBs at centromeres increase the R-loop formation, which then leads to the recruitment of BRCA1 and Rad51 to the centromeres and suppression of centromere instability through the activation of HR. Most importantly, Zhu and colleagues showed that BRCA1 deficiency induces over-active transcription of the alpha satellite repeats and alters the heterochromatin at the centromere, leading to increased DNA damage at centromere (Zhu et al., 2011).

PARP1 can also be found at active centromeres (Earle et al., 2000; Saxena et al., 2002b). For example, in mouse embryonic stem cells, robust interactions can be detected between PARP1 and CENP-A, and between PARP1 and CENP-B, two proteins that play a crucial role in maintaining the heterochromatin status at centromeres (Saxena et al., 2002a). Intriguingly, Gemble and colleagues showed that in the cytidine deaminase deficient cells, an important enzyme that is involved in the pyrimidine salvage pathway, excessive dCTPs can also inhibit PARP1, leading to DNA replication defects and formation of the ultrafine anaphase bridges (UFBs) via centromeres and common fragile sites (Gemble et al., 2015). The formation of UFBs are indicative of incomplete DNA replication or entangled HR intermediates (Bizard and Hickson, 2018). These data demonstrated a crucial role of PARP1 in the DNA replication at centromeres and the common fragile sites, likely through remodeling the heterochromatin status (Dantzer and Santoro, 2013).

Ribosomes are cellular machinery where all the cellular proteins are translated. Ribosomes are ribonucleoprotein complex (RNPs) that are made up of many proteins and RNAs, which are called ribosomal proteins and ribosomal RNA (rRNA) respectively. In humans, there are four different rRNAs: 5S, 18S, 5.8S, and 28S, which are transcribed by RNA polymerase I and III. The 5S rRNA (∼150 nucleotides) is transcribed from a cluster of repeated 2.2 kb long genes on 1q42 (Sorensen et al., 1991). The other three rRNAs (18S, 5.8S, and 28S) are generated through post-transcriptional processing of a 45S precursor RNA transcribed from clusters of repeated 43 kb long genes on 13p12, 14p12, 15p12, 21p12, and 22p12 (Henderson et al., 1972). The genomic regions that encode the rRNA are collectively called the rDNA loci (Figure 1D and Table 3), which are the most actively transcribed genomic regions in proliferating human cells (Lane and Fan, 2015). The increased transcriptional activity at the rDNA loci greatly increases the likelihood of collision between the two cellular machineries: the RNA polymerase complexes responsible for transcription and the DNA polymerase complexes responsible for DNA replication. This collision is known as the transcription-replication conflict (TRC).

Using chromatin immunoprecipitation (ChIP) assay, Johnston and colleagues demonstrated that BRCA1 associates with the rDNA loci in multiple breast cancer cell lines (Johnston et al., 2016). Additionally, they also showed that BRCA1 interacts with RNA polymerase I and regulates the transcription of rRNAs. Intriguingly, a recent study by Chang and colleagues showed that the C-terminus domain of BRCA1, i.e., the BRCT domain, facilitates the hybridization of rRNA and the antisense-rRNA thus preventing the formation of R-loops between rRNA and rDNA, and avoiding DNA damage at the rDNA loci (Chang et al., 2022).

Also using the ChIP assay, Guetg and colleagues showed that PARP1 also associates with the rDNA loci (Guetg et al., 2012). Interestingly, they also found that PARP1 binds TIP5, a key component of NoRC and facilitates the re-establishment of heterochromatin in the rDNA loci after their DNA replication.