Literature DB >> 20495751

Amplification of HER-2 gene in breast cancer: immunohistochemical and FISH assessment.

Alina Belengeanu1, Anca Mureşan, Dorina Stoicănescu, Elena Lazăr.   

Abstract

The invasive mammary cancer is the most frequent malignant tumor of women. Different inherited or acquired molecular genetic alterations have been identified in human breast cancers. A fraction of these cancers, as part of their development, undergoes gene amplification. Among the potential prognostic factors are included the biomarkers which measure or are associated with biological processes involved in tumor progression. Evaluation of HER-2 status is important in the management of patients with breast carcinoma, especially for the identification of those who are eligible for immunotherapy. The aim of our study was to evaluate HER-2 amplification status of human breast cancers by FISH and immunohistochemistry. From the total of 50 tumors included in the study, 17 (34%) presented different degrees of positivity; 33 (66%) did not express the oncoprotein HER-2. HER-2 gene and chromosome 17 status were tested in HER-2 2+ cases using FISH technique. FISH analysis may be useful to better evaluate HER-2 status in breast cancer in uncertain cases, where the immunohistochemistry score is 2+. HER-2 testing results have an important role in the clinical management of breast cancer patients. The identification of HER-2 positive tumors is certainly crucial in order to identify patient candidates for anti-HER-2 therapies.

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Year:  2010        PMID: 20495751

Source DB:  PubMed          Journal:  Rom J Morphol Embryol        ISSN: 1220-0522            Impact factor:   1.033


  2 in total

1.  Circulating HER-2 mRNA in the peripheral blood as a potential diagnostic and prognostic biomarker in females with breast cancer.

Authors:  Yanlin Wu; Qiping Meng; Zhixue Yang; Lili Shi; Rongkuan Hu; Peizhuo Zhang; Jinrong Wei; Jie Ren; Bingjing Leng; Dong Xu; Guo-Qin Jiang
Journal:  Oncol Lett       Date:  2018-07-05       Impact factor: 2.967

2.  De novo 8p21.3→ p23.3 Duplication With t(4;8)(q35;p21.3) Translocation Associated With Mental Retardation, Autism Spectrum Disorder, and Congenital Heart Defects: Case Report With Literature Review.

Authors:  Cristina Gug; Dorina Stoicanescu; Ioana Mozos; Laura Nussbaum; Mariana Cevei; Danae Stambouli; Anca Gabriela Pavel; Gabriela Doros
Journal:  Front Pediatr       Date:  2020-07-08       Impact factor: 3.418

  2 in total

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