Study of BRCA1 and BRCA2 Gene Mutations and Clinicopathological Criteria of Breast Cancer in Thi-Qar
Keywords:
breast cancer, BRCA1, BRCA2, gene analysis, PCRAbstract
Breast cancer is the commonest type of malignancy in Iraq. For this reason we study risk factors that associated with this disease in Thi Qar province patients. Such as mutations of breast cancer susceptibility genes 1 and 2 (BRCA1 and BRCA2), clinicopathological parameter ( age, family history and tumor site) . Eighty five blood samples were taken from patients who attended Al-Hussain teaching hospital and oncology unit in Al-Habboby hospital during the period (from August /2014 to April /2017) , fifty blood samples were collected from healthy women as a control. Blood samples were using in genetic study. For histopathological analysis fifty tissue samples were collected from fifty patients with breast cancer who were undergoing surgical resection (mastectomy) to prepare paraffin embedded blocks which have been used for histopathological diagnosis. The present study results revealed that a highest incidence of breast cancer occur in the age group between 40-49 years of age (41%),there is a significant difference among patients age groups (P ≤ 0.01). Family history of breast cancer indicates a strong association with risk of developing breast cancer. The present study showed that family history positive in 31 cases (36.47%), and 54 cases (63.52%) had negative family history of breast cancer. Also the results of present study showed that the 34 cases (41.5%) had first birth at age (20-29years), 18 cases (23.37%) had their first birth in age groups (15-19 years) and (30-39 years), and 7 cases (9.09%) had first birth at age (≥40 years). Most of patients (50.5%) breast cancers were located in right breast and (38.8%) of cases breast cancers were located in left side. Histopathologically, carcinoma was divided into 44 cases (88%) were ductal carcinoma {from which 42 cases(84%) were invasive ductal carcinoma, and 2 cases (4%) were comedocarcinoma}, and 6 (12%) cases were invasive lobular carcinoma. Results revealed that 2 cases (4%) were stage I, 13 cases (26%) were stage II, 24 cases (48%) were stage III and 11 cases (22%) were stage IV, also our results showed that 2 cases (4%) were grade I, 23 cases (46%) were grade II, and 25 cases (50%) were grade III. The DNA was extracted from blood samples by using Accupower® genomic DNA extraction kit. The concentration and purity of all DNA samples have been measured by Nanodrop. Samples with a purity ranged from 1.7 to 1.9 have been enrolled in this study for the molecular detection of BRCA1/2 gene mutation in patients and control groups. In 85 cases of breast cancer, detection of BRCA1/2 gene mutation by multiplex PCR done for the serum revealed that; (185 del AG) mutation in BRCA1 gene was detected in 6 patients (7.05%), and (5382 ins C) mutation in the same gene was detected in 2 patients (2.35%). Regarding (6174 del T) mutation in BRCA2 gene was detected in 3 patients (3.52%). In the control patients gene mutations of any types didn’t detected.References
-Bray F., Ren JS.,Masuyer E., Ferlay J. (2012). Global estimates of cancer prevalence for 27 sites in the adult population in 2008. Int. J. Cancer, 132: 1133-1145.
-Iraqi national cancer research center, (2013). Brief historical introduction,establishing the breast & cervical cancer research unit and the Iraqi National Cancer Research Center/Program.
-Milne, RL. And Antoniou, AC. ( 2011) . Genetic modifiers of cancer riskfor BRCA1 and BRCA2 mutation carriers. Annals of oncology : officialjournal of the European Society for Medical Oncology / ESMO, 22 Suppl 1: i11-7.
- Veltman J., Mann R., Kok T., Obdeijn IM., Hoogerbrugge N.,Blickman JG., et al. ( 2008 ) . European Radiol , 18(5): 931-938.
- Fattahi ,MJ., Mojtahedi, Z., Karimaghaee, N., Talei, A., Banani, SJ.,Ghaderi, A. (2009). Arch Iranian Med; 12(6): 584-587.
-Chan, PC., Wong, BY., Ozeelik, H., Cole,DE. (1999). Simple and rapiddetection of BRCA 1 and BRCA 2 mutation by multiplex mutagenicallyseparated PCR Clin Chem, 45 : 1285-1287.
-Alwan N.A. (2010). Breast cancer: demographic characteristics and clinicopathological presentation of patients in Iraq. EM HJ., 16: 1159-1164.
-Fayaza M S., El-Sherifya M S., El-Basmyb A., Zloufa SA., NazmyaN., Samira S., Attiaa G., and Eissaa H. (2014). Clinicopathological features and prognosis of triple negative breast cancer inKuwait: A comparative/perspective analysis. Reports of practical oncologyand radiotherapy ; 19 (173–181).
-Darweesh A. (2009). Risk factors of breast cancer among Palestinian women in North West bank , An-Najah National University, Nablus, Palestine.
- Nyante SJ., Dallal CM., Gierach GL., Park Y., Hollenbeck AR., Brinton LA. (2013). Risk factors for specific histopathological types ofpostmenopausal breast cancer in the NIH-AARP Diet and Health Study.American journal of epidemiology, 178:359-71.
-Shantakumar S., Terry MB., Teitelbaum SL., Britton JA., MillikanRC., Moorman PG., Neugut. AI, Gammon MD. (2007). Reproductivefactors and breast cancer risk among older women. Breast Cancer ResTreat,102:365-374.
-Zeeneldin AA., Ramadan M. , Gaber A., Taha FM. (2013). Clinicopathological features of breast carcinoma in elderly Egyptian patients: Acomparison with the non-elderly using population-based data. Journal of theEgyptian National Cancer Institute, 25, 5–11.
-Ackerman. ( 2016 ) . Ackerman's surgical pathology . Tenth edition . Adem , C ., Reynolds , C ., Soderberg , CL ., Slezak , JM ., Mc Donnel ,SK ., Sebo , TJ ., Schaid , DJ ., Myers , JL ., Sellers, TA ., Hartmann ,LC ., Jenkins , RB . ( 2003 ) . Pathologic characteristics of breast parenchyma in patients with hereditary breast carcinoma, including BRCA1 and BRCA2 mutations carriersCancer, 97:1-11.
-Alwan N.A. (2010). Breast cancer: demographic characteristics and clinicopathological presentation of patients in Iraq. EM HJ., 16: 1159-1164.
-Pourzand A., Fakhree MB., Hashemzadeh S., Halimi M., Daryani A. (2011).Hormone Receptor Status in Breast Cancer and its Relation to Age and Other Prognostic Factors. Breast Cancer: Basic and Clinical Res, 5:87-92.
-Hamel N., Feng BJ., Foretova L., et al. ( 2011 ). “On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations,” European Journal of Human Genetics, vol. 19, no. 3, pp. 300–306.
-AL-Thaweni, A N., Yousif, WH., Hassan, SS. (2010). Detection ofBRCA1and BRCA2 mutation for Breast Cancer in Sample of Iraqi Womenabove 40 Years. Baghdad Science Journal 7(1).
-Hansa, J., Kannan, R., Ghosh, SK. (2012). Screening of 185DelAG,1014DelGT and 3889DelAG BRCA1 Mutations in Breast Cancer Patientsfrom North-East India . Asian Pacific J Cancer Prev, 13 (11), 5871-5874.
-Al-Mowali, AA., Al-Haroon, SS., and Abdualah , SA. (2014). Study ofBRCA1 and BRCA2 Gene Mutations in Relation to ClinicopathologicalCriteria of Breast Cancer in Basrah. RJPBCS 5(5) 1217.
-John , EM., Miron, A ., Gong, G., et al. ( 2007 ) . “Prevalence of pathogenicBRCA1 mutation carriers in 5 US racial/ethnic groups,” Journalof theAmerican Medical Association, vol. 298, no. 24, pp. 2869–2876 .
-Armaou, S., Pertesi, M., Fostira, F., Thodi, G., Athanasopoulos, PS.,Kamakari, S.,Athanasiou, A., Gogas, H., Yannoukakos, D., Fountzilas, G.,Konstantopoulou, I. (2009). Contribution of BRCA1 germ-line mutations tobreast cancer in Greece a hospital-based study of 987 unselected breast cancercases. Br J Cancer, 101:32-37.
-Mehdipour , P., Hosseini-Asl, S., Savabi-E, A., Habibi, L., Alvandi ,E.,Atri, M.( 2006 ) . Low Frequency of 185delAG Founder Mutation of BRCA1Gene in Iranian Breast Cancer Patients. Journal of Cancer Molecules; 2(3):123-127.
-Fattahi ,MJ., Mojtahedi, Z., Karimaghaee, N., Talei, A., Banani, SJ.,Ghaderi, A. (2009). Arch Iranian Med; 12(6): 584-587.