Abstract
Introduction
The role of the BRCA1 and BRCA2 genes in bladder and renal tumorigenesis is unclear. Our goal was to determine the prevalence of specific founder mutations genes BRCA1 (5328 insC, C61G and 4153 delA) and BRCA2 (C5972T) mutations in bladder and kidney cancer patients from Poland.
Materials and methods
We genotyped 1028 patients with bladder cancer and 688 cases with kidney cancer and two control groups.
Results
A BRCA1 mutation (all variants combined) was detected in peripheral blood leukocytes in 5 out of 1028 (0.5%) bladder cases and in 17 of 4000 controls (0.4%) (odds ratio [OR], (OR = 1.1; 95% CI 0.42–3.11; p = 1.0). Among 688 unselected kidney cancer cases a BRCA1 mutations was reported in three patients (0.4%) (OR = 1.0; 95% CI 0.29–3.51; p = 1.0). The mutation C5972T in BRCA2 was observed in 54 bladder cancer patients (5.2%) and in 159 of 2791 healthy controls (5.7%) (OR = 0.9; 95% CI 0.66–1.26; p = 0.6). Fifty kidney cancer cases carried a BRCA2 mutation (7.3%) (OR = 1.3; 95% CI 0.93–1.80; p = 0.1).
Conclusion
In conclusion, we found no difference in the prevalence of BRCA1 and BRCA2 founder mutations between cases and healthy controls. The mutations BRCA1 and BRCA2 seem not to play a role in bladder and kidney cancer development in Polish patients.
Keywords: Mutation: 5328 insC, C61G, 4153 delA, C5972T; gene: BRCA1, BRCA2
Introduction
Bladder cancer is the second most common malignant neoplasm of the genitourinary system in men. Bladder malignancies are responsible for approximately 5% of deaths in men and 2% in women. Currently, kidney cancer accounts for approximately 3% of all cancers diagnosed in adults. Malignant neoplasms account for approximately 3% of male deaths and 2% of female cancers [1]. So far, the molecular basis for the development of a small percentage of bladder and kidney cancers has been identified. High hereditary predisposition for bladder and kidney cancer is presents in 4 and 5% respectively [2, 3]. Most cancers result from a complex interaction of environmental and genetic factors.
The genes BRCA1 and BRCA2 belongs to antioncogenes, inhibit the cell proliferation process, induce the process of apoptosis, maintain the stability of the genetic material, repair damage and changes that occur at the DNA level [4]. Mutations of BRCA1 gene are the cause of 50–80% risk of breast, 40% ovarian cancer and in 40–50% of familial site-specific breast cancers [5–7]. Mutations in the BRCA2 gene are responsible for tumors in breast cancer in 31–56%, ovarian cancer 11–27% and have been found in families with male breast cancers [8, 9]. Moreover changes in the BRCA1 and BRCA2 genes show an increased risk for the formation of neoplasms of other organs, including cancers of the: prostate, fallopian tube, pancreatic, bladder or melanoma [10–16].
To our knowledge, this is the first large-scale study to survey patients with bladder and kidney cancer for mutations in BRCA1 gene (5328 insC, C61G and 4153 delA) and BRCA2 (C5972T). To establish whether or not the mutations in the BRCA1 and BRCA2 genes contribute to bladder or kidney cancer in Poland, and to measure the impact of this variant on cancer risk, we genotyped 1028 unselected patients with bladder cancer, 688 unselected cases with renal cancer, 4000 healthy controls for testing the BRCA1 gene and 2791 healthy controls for testing BRCA2 gene.
Material and methods
Patients
We studied a series of 1028 unselected cases with urothelial bladder cancer (268 women and 760 men) and 688 unselected kidney cancer patients (284 women and 404 men) diagnosed at the Urology Hospital in Szczecin and the Genetic outpatients clinic between 2000 and 2018. A total of 1518 incident cases of bladder cancer and 869 kidney cancer were identified during the study period. Of these, 1419 patients with bladder (93%) and 835 with kidney cancer (96%) accepted the invitation to participate in the study. During the interview at the Genetic outpatients Clinic the goals of the study were explained, informed consent was obtained, family history and smoking status were collected, genetic counseling was given and a blood sample was taken for DNA analysis. The pathological diagnosis of bladder and kidney cancer was confirmed by biopsy review at a single central pathology laboratory in Szczecin, Poland. All cases were unselected for age, sex, smoking status and family history. The mean age of diagnosis for bladder cancer patients was 67 years (range 25–91) and was 64 years (range 17–91) for kidney cancer patients. A family history was taken by the construction a pedigree and questionnaire. A total of 40 patients with a family history of at least 1 bladder cancer in their first or second degree relatives and 27 cases with a family history of at least 1 kidney cancer in first or second degree relatives were identified. The vital status and the date of death of all of the cases were obtained from the Polish Ministry of the Interior and Administration in February 2021. In total we received information of 580 (56%) patients with bladder cancer and 233 (34%) with kidney cancer had died. All patients and control subjects are of European ancestry and are ethnic Poles. The study was approved by the Ethics Committee of Pomeranian Medical University in Szczecin.
Controls
We used two control groups. The first control group included 4000 unselected, cancer-free individuals. These controls were selected to investigate the potential association between three Polish founder mutations of BRCA1 gene (5328 insC, C61G and 4153 delA) and bladder and kidney cancer. This controls were taken from 1000 adult patient (age range 15–91, mean 58.3) lists of three family doctors from Szczecin, 1000 adults (age range 18–35, mean 24.3) from Szczecin who submitted blood for paternity testing and 2000 neonates from ten hospitals throughout Poland. This control group was described in detail elsewhere [17].
The second control group consisted of 2791 unselected, cancer-free individuals to estimate the association between the C5972T variant of BRCA2 gene and bladder and kidney cancer. This control group consisted of 1993 newborn children from 10 hospitals throughout Poland and 798 adults (age range 19–89, mean 58.0) from Szczecin region unselected for family history. This control group was described in detail elsewhere [18].
To ensure comparability of the control groups, the allele frequencies was computed separately for the adult and neonatal control groups, and compared. The allele frequencies for BRCA1 and BRCA2 gene in our control groups were not dependent on age or sex, and the prevalence estimates of mutations in all genes were similar in younger and in older controls. Cases and controls are all residents of Szczecin and were Polish.
Methods
DNA was extracted from peripheral blood for all cases and controls. The two mutations in BRCA1 gene (5328 insC and 4153 delA) were detected by ASO-PCR analyses as described previously [19]. The third mutation in BRCA1 (C61G) and variant C5972T of BRCA2 were genotyped with a TaqMan assay (Life Technologies, Carlsbad, CA) using a LightCycler Real-Time PCR 480 System (Roche Life Science, Mannheim, Germany). The mutations were confirmed by Sanger direct sequencing, using a BigDye Terminator v3.1 Cycle Sequencing Kit (Life Technologies), according to the manufacturer’s protocol. In all reaction sets, positive and negative controls (without DNA) were used.
Statistical analysis
Odds ratios
The prevalence of BRCA1 and BRCA2 allele were compared in bladder cancer cases and in controls, singly and in combination. Odds ratios were generated from two-by-two tables and statistical significance was assessed using the Fisher exact test where appropriate.
Ethical statement
The study was performed in accordance with the principles of the Declaration of Helsinki. All patients and controls provided written informed consent.
Results
Bladder cancer
Gene BRCA1
The 1028 bladder cancer cases and 4000 controls were successfully genotyped for the BRCA1 (5328 insC, C61G, 4153 delA) mutations (Table 1). The five (0.5%) carried a BRCA1 mutation (all variants combined) (OR = 1.1; 95% CI 0.42–3.11; p = 1.0), including three (0.3%) cases with the 5328 insC mutation (OR = 0.8; 95% CI, 0.23–2.90; p = 0.8) and two (0.2%) patients with the C61G mutation (OR = 3.9; 95% CI, 0.54–27.7; p = 0.4). We did not find the mutation 4153 delA in any patient with bladder cancer.
Table 1.
Effect of BRCA1 and BRCA2 mutations on bladder cancer risk
| Mutation subjects | Number of carriers/total (frequency %) | OR | 95% CI | p-value |
|---|---|---|---|---|
| BRCA1 | ||||
| 5328 insC | ||||
| Controls | 14/4000 (0.003) | 1.0 | ||
| Cases | 3/1028 (0.003) | 0.8 | 0.23–2.90 | 0.8 |
| C61G | ||||
| Controls | 2/4000 (0.0005) | 1.0 | ||
| Cases | 2/1028 (0.002) | 3.9 | 0.54–27.7 | 0.4 |
| 4153 delA | ||||
| Controls | 1/4000 (0.0002) | 1.0 | ||
| Cases | 0/1028 | – | – | – |
| All BRCA1 | ||||
| Controls | 17/4000 (0.004) | 1.0 | ||
| Cases | 5/1028 (0.005) | 1.1 | 0.42–3.11 | 1.0 |
| BRCA2 | ||||
| C5972T | ||||
| Controls | 159/2791(0.06) | 1.0 | ||
| Cases | 54/1028 (0.05) | 0.9 | 0.66–1.26 | 0.6 |
The mutation 5328 insC was seen only in the group of 760 affected men (0.4%). The examined change was not observed in 40 family cases with bladder cancer in first- and/or second-degree relatives. Two patients with cancer cases and 5328 insC mutation died within a year of diagnosis and third to February 2021 was still alive.
Gene BRCA2
Of the bladder cancer patients enrolled in the study, fifty four (5.2%) carried a BRCA2 mutation (C5972T) (OR = 0.9; 95% CI 0.66–1.26; p = 0.6) A C5972T mutation was seen in the 36 affected men (4.7%) and in 18 women (6.7%). Among cases with mutations 35 persons were smokers (5.2%). The mutation C5972T was seen in two family cases with bladder cancer in first- and/or second-degree relatives.
Kidney cancer
Gene BRCA1
In total, 688 kidney cancer cases were genotyped for BRCA1 mutations (5328 insC, C61G, 4153 delA) (Table 2). The three (0.4%) cases carried a BRCA1 mutation (5328 insC) (OR = 1.2; 95% CI, 0.35–4.35; p = 1.0). The mutations C61G and 4153 delA had not been found among renal cancer patients.
Table 2.
Effect of BRCA1 and BRCA2 mutations on kidney cancer risk
| Mutation subjects | Number of carriers/total (frequency %) | OR | 95% CI | p-value |
|---|---|---|---|---|
| BRCA1 | ||||
| 5328 insC | ||||
| Controls | 14/4000 (0.003) | 1.0 | ||
| Cases | 3/688 (0.004) | 1.2 | 0.35–4.35 | 1.0 |
| C61G | ||||
| Controls | 2/4000 (0.0005) | 1.0 | ||
| Cases | 0/688 | – | – | – |
| 4153 delA | ||||
| Controls | 1/4000 (0.0002) | 1.0 | ||
| Cases | 0/688 | – | – | – |
| All BRCA1 | ||||
| Controls | 17/4000 (0.004) | 1.0 | ||
| Cases | 3/688 (0.004) | 1.0 | 0.29–3.51 | 1.0 |
| BRCA2 | ||||
| C5972T | ||||
| Controls | 159/2791(0.06) | 1.0 | ||
| Cases | 50/688 (0.07) | 1.3 | 0.93–1.80 | 0.1 |
One man (0.2%) and two females (0.7%) were carriers of the mutation 5328 insC.
This man smoked and died one year after kidney cancer was diagnosed unlike women who had not smoked and to February 2021 was still alive.
Gene BRCA2
The mutation C5972T was seen in the group of fifty (7%) patients with kidney cancer, 28 (10%) women and 22 (5.4%) men, (OR = 1.3; 95% CI, 0.93–1.80; p = 0.1). 17 cases were smokers (6.5%). The mutation in gene BRCA2 has been observed in two family cases with kidney cancer in first- and/or second-degree relatives.
Discussion
The results of our unselected cohort 1028 bladder, 688 kidney cancer cases and two groups of controls 4000 and 2791 revealed no statistical significant difference, indicating that three mutations of BRCA1 gene (5328 insC, C61G, 4153 delA) and one mutation of gene BRCA2 (C5972T) do not seem to play a role in bladder or kidney cancer development.
Inherited changes in genes are the starting point for the development of almost all cancers. This was demonstrated for the first time in a breast cancer model that constitutional genetic markers associated with an increased risk of cancer occur in more than 90% of patients [20, 21]. The above data do not mean that only genetic factors are involved in carcinogenesis. It is already known that even at such a high risk of cancer as e.g. 80% risk of developing breast/ovarian cancer in carriers of the BRCA1 mutation also constitute a significant share among carcinogenic factors environmental factors that may have the character of chemical factors (carcinogens contained in tobacco smoke, alcohol, arsenic concentration), physical (ionizing radiation, UV), biological (oncogenic HPV, EBV viruses) also constitute a significant share among carcinogenic factors [22]. Constitutional genetic changes most often predispose to cancers that develop as a consequence of the existence of multi-gene or monogenic predisposition, which may be associated with a high or moderately increased risk of developing cancer [23]. The cause of cancer may be mutation/ polymorphism in protooncogenes, suppressor genes (anti-oncogenes), DNA damage repair genes (mutator genes), or in genes that metabolize carcinogens and co-carcinogens.
In the literature there are several studies of mutation in the BRCA1 and BRCA2 genes and association with different cancers. Lubiński et al. observed in Polish patients based on studies of subsequent breast/ovarian cancers risks up to 75 years of age, respectively, about 66% for breast cancer and 44% for ovarian cancer [24]. The risk depends on the type of mutation and the location in the gene. The risk of developing breast cancer is about 2 times higher in carriers of the 5382insC mutation compared to the risk in carriers4153delA. An additional factor influencing the level of risk is the cancer family history. Metcalfe et al. found that the risk of breast cancer increases by another 20% for each first-degree relative who develops breast cancer before the age of 50. While the occurrence of ovarian cancer in any first or second degree relative is associated with a 60% higher risk of ovarian cancer [25].
Place of residence also affects the level of risk. In a prospective cancer risk study, penetration differences depending on the place of residence were found. The probability of developing breast cancer up to the age of 70 for carriers of the BRCA1 gene mutation from North America was estimated at 72% and for carriers from Poland at 49%, indicating the importance of environmental factors [26]. Characteristic of ovarian cancers in carriers of the BRCA1 mutation is also an increased risk of fallopian tube and peritoneal cancers, estimated at about 10%. Most likely, the risk of other organ cancers in some types of BRCA1 mutations is also increased, however, this brca1-carrying effect has not been definitively proven so far. As shown by studies of 200 Polish families with strong aggregation of breast/ovarian cancers, constitutional mutations of the BRCA2 gene are rare in this group, with a frequency of about 4%. The most of the BRCA2 mutations occurring in our population, most probably, slightly increases the risk of breast cancer, although studies performed in New Medical Technology Center have shown that in families with aggregation of breast cancer diagnosed before the age of 50 and stomach diagnosed in men before the age of 55, the frequency of the BRCA2 gene mutation is at the level of 10–20% [27]. Mutations in the BRCA2 gene, are associated with a significant, although more precisely undefined, risk of: ovary, prostate cancer and cancers of the gastrointestinal tract: stomach, colon, pancreas [28]. This is supported by the research carried out in New Medical Technology Center, in which mutations were detected with a frequency of about 30% in families without breast cancer, but with aggregation of ovarian cancer and cancer of the stomach, colon or pancreas among relatives I0 lub II0 [28]. The research conducted in Poznań shows that the frequency of mutations of the BRCA2 gene is also increased in families with breast cancer in men and it amounts to about 15% in Poland [29]. In a recent study, Nassar et al. demonstrated that the BRCA2 gene is significant associated with bladder cancer [15]. They detected pathogenic variants of the BRCA1 gene in 2.3% and the BRCA2 gene in 2.1% in patients with urothelial carcinoma. Another report on 98 patients with bladder cancer showed that mutations in DNA repair genes (CHEK2, ERCC5, GEN1, MLH1, PALB2, RAD50, RAD51B and RECQL4) are associated with an unfavorable cancer prognosis and 22% of patients had a mutation [30]. In the Sweis et al. study, we noticed that changes to the BRCA1, BRCA2, ERCC2 and ATM genes occur in 25% of urothelial carcinoma patients [14].
There are several strengths of our study including the large number of patients and controls, and the sampling of incident cases, unselected for age or family history. There is no reason to believe that age, sex or smoking behavior are important confounders of the observed association.
Our study was not without limitations, including a lack of information on histological features and smoking behavior in all patients.
Conclusion
In conclusion, this study reveals that mutations in BRCA1 gene (5328 insC, C61G, 4153 delA) and mutation (C5972T) of gene BRCA2 did not seem to play a major role in bladder or kidney cancer development. Our results indicate that testing mutations are unlikely to be relevant for the identification of individuals at risk of bladder or kidney cancer, at least in the Polish population.
Acknowledgements
We thank: Marcin Słojewski, Thierry van de Wetering, Cezary Cybulski, Anita Giermakowska, Joanna Trubicka, Artur Lemiński, Michał Soczawa for support in this study.
Authors’ contributions
EZ-P - wrote the manuscript, carried out the molecular genetic studies, performed the statistical analysis; AT-G - enrolled the patients into the study group; SAN, JL - critically revised the manuscript and approved its final version. All authors read and approved the final version of the manuscript.
Funding
This study was funded by Pomeranian Medical University, Szczecin. These authors are employees of Pomeranian Medical University, Szczecin: EZP, ATG, SAN, JL. The specific roles of these authors are articulated in the ‘author contributions’ section. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
Our data contain potentially sensitive information therefore we have not included it with our manuscript. Those who would like to request access to data may contact Melissa Sidhu at the Research Ethics Board of Women’s College Hospital by calling (416) 351–3732 × 2723 or email ac.latipsohcw@uhdis.assilem. The Pomeranian University of Medicine Ethics Committee will grant access to all researchers who meet the criteria for access to confidential data.
Declarations
Ethics approval and consent to participate
The study was approved by Ethics Committee of the Pomeranian Medical University in Szczecin, Poland. All participants gave informed written consent prior blood donating.
Consent for publication
Not applicable.
Competing interests
JL is CEO of Read-Gene S.A. The authors EZ-P, AT-G, SAN declare that they have no conflict of interest relevant to this article.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Elżbieta Złowocka-Perłowska, Aleksandra Tołoczko-Grabarek, Steven A. Narodand Jan Lubiński have contributed equally to this work.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Our data contain potentially sensitive information therefore we have not included it with our manuscript. Those who would like to request access to data may contact Melissa Sidhu at the Research Ethics Board of Women’s College Hospital by calling (416) 351–3732 × 2723 or email ac.latipsohcw@uhdis.assilem. The Pomeranian University of Medicine Ethics Committee will grant access to all researchers who meet the criteria for access to confidential data.