Literature DB >> 22434244

Hereditary breast cancer: practical pursuit for clinical translation.

Henry T Lynch1, Carrie Snyder, Jane Lynch.   

Abstract

The benefits of a skillful medical history and histologic confirmation of relevant pathology are potentially lifesaving. Appropriately directed DNA testing based on these initial steps provides an opportunity for clinical translation into a cancer prevention program targeted to family members. Unfortunately, cancer prevention strategies that are based on genetics are frequently overlooked or underestimated in the overall practical management of patients at high risk for breast cancer as well as integral cancers that constitute a hereditary breast cancer syndrome. DNA testing, particularly for BRCA1 and BRCA2 in hereditary breast-ovarian cancer syndrome and p53 in the Li-Fraumeni syndrome, and many other syndromes is commercially available for inclusion in a cancer control program and merits attention in this major public health problem. It is clear that the time and effort expended for a hereditary cancer syndrome diagnosis may significantly reduce both morbidity and mortality in breast cancer. We have found that genetic counselors can partner with the clinical physicians and make significant contributions to this labor-intensive effort.

Entities:  

Mesh:

Year:  2012        PMID: 22434244     DOI: 10.1245/s10434-012-2256-z

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  9 in total

1.  A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancer.

Authors:  Natalie J Engel; Patricia Gordon; Darcy L Thull; Beth Dudley; Judy Herstine; Rachel C Jankowitz; Kristin K Zorn
Journal:  Fam Cancer       Date:  2012-09       Impact factor: 2.375

2.  Differences in DNA methylation by extent of breast cancer family history in unaffected women.

Authors:  Lissette Delgado-Cruzata; Hui-Chen Wu; Yuyan Liao; Regina M Santella; Mary Beth Terry
Journal:  Epigenetics       Date:  2013-10-29       Impact factor: 4.528

3.  Multicenter cross-sectional screening of the BRCA gene for Chinese high hereditary risk breast cancer populations.

Authors:  Hongyi Wei; Minghao Wang; Jianghua Ou; Weihua Jiang; Fuguo Tian; Yuan Sheng; Hengyu Li; Hong Xu; Ruishan Zhang; Aihua Guan; Changqing Wang; Hongchuan Jiang; Yu Ren; Jianjun He; Jian Liu; Weiwei Huang; Ning Liao; Xiangjun Cai; Jia Ming; Rui Ling; Yan Xu; Chunyan Hu; Jianguo Zhang; Baoliang Guo; Lizhi Ouyang; Ping Shuai; Zhenzhen Liu; Ling Zhong; Ruilin Jing; Zhen Zeng; Meng Zhang; Ting Zhang; Zhaoling Xuan; Xuanni Tan; Junbin Liang; Qinwen Pan; Li Chen; Fan Zhang; Linjun Fan; Yi Zhang; Xinhua Yang; Jingbo Li; Chongjian Chen; Jun Jiang
Journal:  Oncol Lett       Date:  2018-04-18       Impact factor: 2.967

4.  Knowledge about hereditary cancer of women with family histories of breast, colorectal, or both types of cancer.

Authors:  N Campacci; J O de Lima; L Ramadan; E I Palmero
Journal:  J Cancer Educ       Date:  2015-03       Impact factor: 2.037

5.  Breast Cancer Screening Strategies for Women With ATM, CHEK2, and PALB2 Pathogenic Variants: A Comparative Modeling Analysis.

Authors:  Kathryn P Lowry; H Amarens Geuzinge; Natasha K Stout; Oguzhan Alagoz; John Hampton; Karla Kerlikowske; Harry J de Koning; Diana L Miglioretti; Nicolien T van Ravesteyn; Clyde Schechter; Brian L Sprague; Anna N A Tosteson; Amy Trentham-Dietz; Donald Weaver; Martin J Yaffe; Jennifer M Yeh; Fergus J Couch; Chunling Hu; Peter Kraft; Eric C Polley; Jeanne S Mandelblatt; Allison W Kurian; Mark E Robson
Journal:  JAMA Oncol       Date:  2022-04-01       Impact factor: 33.006

6.  Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry.

Authors:  Gabriela C Fernandes; Rodrigo A D Michelli; Henrique C R Galvão; André E Paula; Rui Pereira; Carlos E Andrade; Paula S Felicio; Cristiano P Souza; Deise R P Mendes; Sahlua Volc; Gustavo N Berardinelli; Rebeca S Grasel; Cristina S Sabato; Danilo V Viana; Edmundo C Mauad; Cristovam Scapulatempo-Neto; Banu Arun; Rui M Reis; Edenir I Palmero
Journal:  Oncotarget       Date:  2016-12-06

7.  Genetic and epigenetic characterization of the BRCA1 gene in Brazilian women at-risk for hereditary breast cancer.

Authors:  Paula Silva Felicio; Matias Eliseo Melendez; Lidia Maria Rebolho Batista Arantes; Ligia Maria Kerr; Dirce Maria Carraro; Rebeca Silveira Grasel; Natalia Campacci; Cristovam Scapulatempo-Neto; Gabriela Carvalho Fernandes; Ana Carolina de Carvalho; Edenir Inêz Palmero
Journal:  Oncotarget       Date:  2017-01-10

8.  Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.

Authors:  Natalia Campacci; Juliana O de Lima; André L Carvalho; Rodrigo D Michelli; Rafael Haikel; Edmundo Mauad; Danilo V Viana; Matias E Melendez; Fabiana de L Vazquez; Cleyton Zanardo; Rui M Reis; Benedito M Rossi; Edenir I Palmero
Journal:  Cancer Med       Date:  2017-10-21       Impact factor: 4.452

9.  Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population.

Authors:  Paula Silva Felicio; Lucas Tadeu Bidinotto; Matias Eliseo Melendez; Rebeca Silveira Grasel; Natalia Campacci; Henrique C R Galvão; Cristovam Scapulatempo-Neto; Rozany Mucha Dufloth; Adriane Feijó Evangelista; Edenir Inêz Palmero
Journal:  Oncotarget       Date:  2018-06-08
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.