Gupta Ishita, Sareyeldin Rasha M, Al-Hashimi Israa, Al-Thawadi Hamda A, Al Farsi Halema, Vranic Semir, Al Moustafa Ala-Eddin
College of Medicine, Qatar University, Doha P. O. Box:2713, Qatar.
Biomedical Research Centre, Qatar University, Doha P.O Box: 2713, Qatar.
Cancers (Basel). 2019 Mar 13;11(3):363. doi: 10.3390/cancers11030363.
Breast cancer is the most frequent cause of cancer-related deaths among women worldwide. It is classified into four major molecular subtypes. Triple-negative breast cancers (TNBCs), a subgroup of breast cancer, are defined by the absence of estrogen and progesterone receptors and the lack of HER-2 expression; this subgroup accounts for ~15% of all breast cancers and exhibits the most aggressive metastatic behavior. Currently, very limited targeted therapies exist for the treatment of patients with TNBCs. On the other hand, it is important to highlight that knowledge of the molecular biology of breast cancer has recently changed the decision-making process regarding the course of cancer therapies. Thus, a number of new techniques, such as gene profiling and sequencing, proteomics, and microRNA analysis have been used to explore human breast carcinogenesis and metastasis including TNBC, which consequently could lead to new therapies. Nevertheless, based on evidence thus far, genomics profiles (gene and miRNA) can differ from one geographic location to another as well as in different ethnic groups. This review provides a comprehensive and updated information on the genomics profile alterations associated with TNBC pathogenesis associated with different ethnic backgrounds.
乳腺癌是全球女性癌症相关死亡的最常见原因。它被分为四种主要分子亚型。三阴性乳腺癌(TNBC)是乳腺癌的一个亚组,其定义为缺乏雌激素和孕激素受体且HER-2不表达;该亚组约占所有乳腺癌的15%,并表现出最具侵袭性的转移行为。目前,用于治疗TNBC患者的靶向治疗非常有限。另一方面,必须强调的是,乳腺癌分子生物学知识最近改变了癌症治疗方案的决策过程。因此,一些新技术,如基因谱分析和测序、蛋白质组学以及微小RNA分析,已被用于探索包括TNBC在内的人类乳腺癌的发生和转移,这可能会带来新的治疗方法。然而,根据目前的证据,基因组图谱(基因和微小RNA)在不同地理位置以及不同种族群体之间可能存在差异。本综述提供了与不同种族背景相关的TNBC发病机制相关的基因组图谱改变的全面且最新的信息。