alexa Screening of BRCA 1 - 185delAG mutation in Ovarian Cancer patients in a Tertiary care centre from Telangana | OMICS International
ISSN: 2161-0932
Gynecology & Obstetrics

Like us on:

Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Screening of BRCA 1 - 185delAG mutation in Ovarian Cancer patients in a Tertiary care centre from Telangana

Sirisha P1*, Vottery R2, Amidyala L2, Nallari P3, Jyothy A1 and Venkateshwari A1

1Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, India

2Yashoda Hospital, Secunderabad, India

3Department of Genetics, Osmania University, Hyderabad, India

Corresponding Author:
Venkateshwari A, Sirisha P
Institute of Genetics and Hospital for Genetic Diseases
Osmania University, Begumpet, Hyderabad - 500016, India
Tel: 091-40-23403681
E-mail: [email protected]

Received Date: July 05, 2017; Accepted Date: July 20, 2017; Published Date: July 25, 2017

Citation: Sirisha P, Vottery R, Amidyala L, Nallari P, Jyothy A, et al. (2017) Screening of BRCA 1 - 185delAG mutation in Ovarian Cancer patients in a Tertiary care centre from Telangana. Gynecol Obstet (Sunnyvale) 7:444. doi: 10.4172/2161-0932.1000444

Copyright: © 2017 Sirisha P, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Gynecology & Obstetrics


Aim: Ovarian cancer (OC) occurs due to genetic alterations and mutations in BRCA gene. The aim of the study is to assess the frequency of genetic alterations that persist in Ashkenazi founder mutation BRCA1, 185delAG in patients with ovarian cancer from South Indian origin.

Materials and Methods: A total of 100 ovarian cancer patients and an equal number of control subjects were included in the present study. Screening of 185delAG mutation BRCA1 gene was carried out by ARMS PCR followed by agarose gel electrophoresis. Statistical analysis was applied to test for the significance of the results obtained.

Results: The genotype distribution of WW, WM, MM showed a significant difference between the two subjects, 95%, 4% and 1% in controls and 52%, 36% and 12% in cases respectively. An increased frequency of homozygotic mutant genotypes (MM) were found in patients compared to controls. Similarly, a significant difference in the distribution of M allele in cases and control subjects (W v/s M: χ2 P<0.0001, OR 18.06, 95% CI 6.31-51.65) was observed.

Conclusion: The demographic details of the patients and controls revealed that females of age greater than 40 years are associated with high risk of ovarian cancer. The postmenopausal women have a very high susceptibility to OC (6.5 times riskier). Therefore, 185delAG mutation BRCA1 has a possible association in the etiology of ovarian cancer.


BRCA1; 185delAG mutation; Ovarian Cancer


Ovarian cancer (OC) is the most common forms of hereditary cancer in women and is the leading cause of death by gynecological malignancy. It has a hostile phenotype and a relatively poor prognosis. More than two thirds of patients were showing late stage disease [1,2]. It is predominantly a disease of postmenopausal women and has an overall 5-year survival of less than 30% [3]. Earlier studies indicate that hereditary cancers constitute 5%-10% and may be up to 14% [4,5] epidemiologic and molecular genetics analyses indicate that about 10% of all epithelial ovarian carcinomas are associated with autosomal dominant genetic predisposition, conferred primarily by inherited mutations in BRCA1 or BRCA2, they account for >90% of hereditary cancers. In general population the frequency ranges between 2-12% and 2-6% respectively [6]. The cumulative life time risk of developing epithelial ovarian carcinoma ranges from 20%-30% [7]. BRCA1 cloned in 1994 and 2 in 1995 both are very large genes most known mutations lead to premature termination of protein, leading to loss of tumor suppression [8]. Mutations in BRCA1 are present in approximately onehalf of the early-onset breast cancer families and 80% of the early-onset breast and ovarian cancer families [9] whereas BRCA2 mutations are believed to account for a comparable percentage of inherited breast cancer cases [10]. Both the genes are detrimental and acts as a sensor for DNA damage [11,12] hence resulting in defects in DNA repair, transcription, abnormal centrosome regulation, impaired spindle check point and chromosome damage. In view of the above the present study is aimed to evaluate the role of the founder mutation in the etiology of ovarian cancer.

Materials and Methods

Study population

A total of 200 individuals were included in the present study. 100 clinically and histopathologically confirmed ovarian cancer patients from Yashoda Hospital, Secunderabad during the years 2012-14 and an equal number of age matched healthy control subjects were also incorporated for comparative studies. A structured proforma was used to seek information on dietary habits, smoking, alcohol consumption, family history etc. Written informed consent was obtained from all the subjects. The study was also approved by our Institutional Ethical committee.

DNA isolation

Five ml of venous blood was drawn from each individual in EDTA vacutainers. Genomic DNA was isolated from whole blood using the salting out method [13].

Mutation analysis of 185delAG

The mutation of 185delAG was analyzed based on Amplification Refractory Mutation System-Polymerase Chain Reaction (ARMSPCR). The BRCA1 185delAG exon 2 primers are as follows: forward primer, 5’- GGTTGGCAGCAATATGTGAA-3’ (P1), Wild-type reverse 5’-GCTGACTTACCAGATGGGACTCTC-3’ (P2) and Mutant reverse5’-CCCAAATTAATACACTCTTGTCGTGACTTACCAGAT GGGACAGTA-3’ (P3). A 335 base pair region for wild type and 354 base pair region for mutant type was targeted for amplification. The optimized reaction conditions consisted of 25 mg of genomic DNA in a reaction volume of 20 μl of reaction mixture consisting of 10 × PCR reaction buffer (10 mM Tris-HCl, pH 8.3, 50 mM KCl, 10 μg/ml gelatin), 3.25 mM MgCl2, 0.2 mM dNTPs, and 3 U Taq DNA polymerase (Roche, Penzberg, Germany), 2.0 μM for P1 and P3, 0.4 μM for P2. The cycling conditions were as follows: an initial denaturation at 94°C for 4 minutes, followed by 35 cycles at 94ºC for 30 s, 57.3° C for 30s and 72°C for 45s. The final extension step was at 72°C for 10 min.

The amplified products were electrophoresed on an agarose gel (2.0%) stained with ethidium bromide. The presence of 335 bp band indicates wild type and 354 bp band indicates mutant type based on 100–base pair ladder.

Statistical analysis

The distribution of BRCA1 185delAG mutation and allele frequencies in healthy and ovarian cancer group were analyzed by Chi-square. Odds ratio (OR) and 95% confidence intervals (95% CI) were also assessed. Differences among subject groups in clinical characteristics were analyzed with Fisher’s two-tailed exact tests. Mutation frequencies were tabulated by direct counting and allele frequencies estimated from the observed number of mutations.


The study population consist of 100 Ovarian cancer patients, comprising 32 familial and 68 sporadic cases including 100 agematched controls were screened for the presence of 185delAG of BRCA1 mutation. Data related to age, marital status, consanguinity, menopause status, familial history, taken into consideration and (Table 1) derived from the same geographic location and are representative of South Indian population from Telangana. There was a significant difference in allele distribution between patients and control subjects (W v/s M: χ2 P<0.0001, OR 18.06, 95% CI 6.31-51.65).

Variables Controls/Patients Odd’s ratio 95% CI p-value
≤40 44/18 6.833 3.413-13.813 0.000**
>40 56/82      
Menopause status
Pre 74/29 6.968 3.582-13.660 0.000**
Post 26/71      
Yes 8/26 0.247 0.097-0.616 0.001*
No 92/74      
Diet Intake
Veg 10/18 0.506 0.204-1.240 0.153
Non-Veg 90/82      
Marital status
Married 86/75 0.246 0.054-0.963 0.037*
Unmarried 14/03      

Table 1: Demographic details of ovarian cancer patients and control subjects.

The demographic features of ovarian cancer patients and controls subjects have been represented on various variables like Age, Menopause Status, Consanguinity, Diet Intake and Marital Status.

The age of incidence of ovarian cancer seems to be population specific. Our ethnic group includes 100 OC patients of which 18% (≤ 40 years of age) and 82% (>40 years of age). Patients and control subjects were derived from the same ethnic group. A significant association of ovarian cancer patients with age (p<0.000), menopausal status (p<0.000), consanguinity (0.043) and marital status (p=0.022). On the other hand, there was no significant association with diet intake. Histopathologically, staging plays a major role, the ovarian tumors falls under major categories (Scully, 1987; Serov, 1973); epithelial, germ cell and sex cord-stromal cell tumors. According to our study, Epithelial (85%); Germ cell (04%); Sex cord-stromal (03%) and Unknown/ unclassified (08%). When taking family history into consideration, the study reflected over 32% are of familial cases and 68% are sporadic cases.

Mutation frequency (185delag) based on family history

Figure 1 shows the mutation-detection rate was dependent on different Cancer Case History that shows: Breast & Ovarian Cancer 7/9 (77.7%); Only Ovarian Cancer 3/4 (75%); History of Other Cancer 10/19 (52.6%); Sporadic Cases 31/68 (45.50%).


Figure 1: HPLC chromatogram of the nine reference compounds in 50% aqueous methanol, measured at 370nm. Retention times for rutin, sutherlandin A, sutherlandin B, kaempferol-3-O-rutinoside, sutherlandin C, sutherlandin D, quercitrin, quercetin and kaempferol were 11.9, 12.7, 13.8, 15.3, 16.2, 17.0, 18.0, 26.2 and 28.1 minutes, respectively.

Frequency of mutations in cases by age

Age has been considered as one of the potential factors for ovarian cancer as the risk increases with the advancement of age and the survival rate decreases accordingly. The average age at diagnosis of ovarian cancer was 52.5 years and the average age of menarche is 12.2 years, respectively. This graph is obtained in accordance with the age specific incidence of Ovarian cancer in south-Indian population. The age of the patients have been categorized into 4 groups ≤ 30 yrs (4); 31-40 yrs (14), 41-50 yrs (29) and ≥ 50 age group (53). However, the overall incidences in different groups were inconsistent and showed peak in ≥ 50 age group (Figure 2). Table 2 shows the distribution of 185delAG mutation of BRCA1 gene in control subjects and patients with ovarian cancer. WW 95%, WM 4% and MM 1% in controls and 52%, WM 36% and MM 12% in cases. An increased frequency of homozygotic mutant genotypes (MM) were found in patients compared to controls. There was a statistically significant difference in the distribution of allele frequencies in cases and controls (W v/s M: χ2 P<0.0001, OR 18.06, 95% CI 6.31-51.65).

Genotype Controls
Odds ratio 95% CI P value
WW 95  (95) 52  (52)      
WM 04  (4) 36  (36) 16.4 5.54-48.7 <0.000**
MM 01  (1) 12  (12) 21.9 2.77-173.3 <0.0001**
Allelic Frequency
W 114 0.730 196 0.98      
M 42 0.269 04   0.02 18.05 6.31-51.65 <0.0001**

Table 2: Distribution of 185delAG mutation and its allelic frequencies in patients and control subjects.


Figure 2: HPLC chromatogram of the nine reference compounds in 50% aqueous methanol, measured at 370nm. Retention times for rutin, sutherlandin A, sutherlandin B, kaempferol-3-O-rutinoside, sutherlandin C, sutherlandin D, quercitrin, quercetin and kaempferol were 11.9, 12.7, 13.8, 15.3, 16.2, 17.0, 18.0, 26.2 and 28.1 minutes, respectively.


In our present study, an increased BRCA1 185delAG is the founder mutation in many ethnic groups. This study supports the concept that the 185delAG of BRCA1 germ line mutation, referred to as ‘Ashkenazi mutation’, which is not restricted to a particular ethnic sub-group [14]. Ashkenazi and a considerable fraction of non-Ashkenazi 185delAG mutation carriers support the concept of a common ancient founder for this particular mutation in Jewish people of different ethnic origin [15]. The study conducted by Saxena et al. [16] on 204 families which included only 34 families had a positive family history [16]. One of the main features of familial breast/ovarian cancer is its early onset; therefore families with an early onset will be considered for BRCA1 and BRCA2 mutation study. But in India, to include such families in the screening program may not be reasonable because it has been reported in population based registries that the average age of breast cancer patients to be 50-53 which in case of American women is 61 years. This is an important fact because 90% of the breast cancers are of sporadic origin. Therefore, if early onset families are included in mutation screening studies, it may lead to compromised estimation of the mutation frequency. As per this study, the frequency of these two gene mutations in familial breast cancer cases was found to be 24.6% and ovarian contributed to 3.28% respectively. In different population it is 21% and 9% in Britain, 24% and 18% in France, 40% and 16% in Canada, and 39% and 25% in the USA, respectively, and in either genes 35% represented in the families of Sweden and Hungary [17].

This mutation occurs in an area of multiple adenosines residues which is prone to DNA slippage, thus indicating that this mutation has sustained the natural selective evolutionary pressure against it, with the finding of an apparent independent focus of its occurrence [18]. As the mutation 185delAG was predominantly detected among Ashkenazi Jews, it has been termed as the “Ashkenazi Mutation” because this group attained 1% carrier frequency within the population since origin of the ancestral mutation [19]. Among the breast/ovarian cancer patients, absence of 185delAG mutation in BRCA1 may be due to mutations in other regions like in non-coding and other coding regions of the gene and in other genes like BRCA2, PTEN, p53 [20-22]. 185delAG mutation is one of the most common mutations, it is located at the 5’ end of the gene and predicted to cause truncation at the beginning of the zinc-binding region of the RING of the putative polypeptide. It was proposed that mutations within the BRCA1 RING domain predispose to cancer by inactivating BRCA1 ubiquitin protein ligase activity [23].

In our present study, an increased frequency of homozygotic mutant genotype (MM) was found and a statistical significant association was noticed in the distribution of 185delAG in patients compared to control subjects. Further studies are required based on mutational analysis for identification of related mutations and polymorphisms. The biological effects of the protein related to polymorphisms can be understood which will help in predicting the etiology of ovarian cancer in different geographical regions. Proper counselling of patients and presymptomatic mutation carriers will help them make better decisions about medical and surgical preventive options.


From this study, we found that the prevalence of 185delAG of BRCA1 gene have shown some similarities and difference when compared with other populations. This study also emphasizes the importance of demographic details which play major role in mutation screening. Patients who are at a high risk of early-onset disease, with appropriate awareness i.e. genetic counselling, counselling should include a discussion of the basic principles of hereditary cancer susceptibility as well as an evaluation of the woman’s own risk of cancer, and how testing would add to the characterization of those risks, and how medical management would be affected by a positive and a negative test result so that patients and carriers would be in safe zone.


The authors are thankful to Mr. P. Madhava Prasad and all the clinical staff of Yashoda Hospitals, Secunderabad.


Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

  • International Conference on Medical and Health Science August 24-25, 2018 Tokyo, JAPAN Theme: Scrutinize the Modish of Medical and Health Science
    August 24-25, 2018 Tokyo, Japan
  • World Summit on Trauma and Reconstructive Surgery Sep 10-11, 2018 Singapore Theme: Expanding new horizons in Trauma and Surgery
    Sep 10-11, 2018 Singapore City, Singapore
  • 6th American Gynecological Surgery Conference September 28-29, 2018 San Antonio | Texas | USA
    September 28-29, 2018 San Antonio, USA
  • World Congress on Fetal and Maternal Medicine October 15-17, 2018 Osaka, Japan Theme: A New Beginning on Fetal, Maternal & Neonatal Medicine
    October 15-17, 2018 Osaka, Japan
  • International Conference on Reproduction and Fertility October 18-19, 2018 Abu Dhabi, UAE
    October 18-19, 2018 Abu Dhabi, UAE

Article Usage

  • Total views: 741
  • [From(publication date):
    July-2017 - Aug 15, 2018]
  • Breakdown by view type
  • HTML page views : 688
  • PDF downloads : 53

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2018-19
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri & Aquaculture Journals

Dr. Krish

[email protected]

+1-702-714-7001Extn: 9040

Biochemistry Journals

Datta A


[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals


porn sex

[email protected]

1-702-714-7001Extn: 9042

Chemistry Journals

Gabriel Shaw

Gaziantep Escort

[email protected]

1-702-714-7001Extn: 9040

Clinical Journals

Datta A


[email protected]

1-702-714-7001Extn: 9037

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

Food & Nutrition Journals

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

General Science

Andrea Jason

mp3 indir

[email protected]

1-702-714-7001Extn: 9043

Genetics & Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Materials Science Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Nursing & Health Care Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Medical Journals


Nimmi Anna

[email protected]

1-702-714-7001Extn: 9038

Neuroscience & Psychology Journals

Nathan T


[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

Ann Jose

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001Extn: 9042

© 2008- 2018 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
Leave Your Message 24x7