Mahmoud Rinad, Ordóñez-Morán Paloma, Allegrucci Cinzia
Centre for Cancer Sciences, Biodiscovery Institute, University of Nottingham, Nottingham NG7 2RD, UK.
Translational Medical Sciences Unit, School of Medicine, University of Nottingham, Nottingham NG7 2RD, UK.
Cancers (Basel). 2022 Sep 1;14(17):4280. doi: 10.3390/cancers14174280.
The Triple Negative Breast Cancer (TNBC) subtype is known to have a more aggressive clinical course compared to other breast cancer subtypes. Targeted therapies for this type of breast cancer are limited and patients are mostly treated with conventional chemo- and radio-therapies which are not specific and do not target resistant cells. Therefore, one of the major clinical challenges is to find compounds that target the drug-resistant cell populations which are responsible for reforming secondary tumours. The molecular profiling of the different TNBC subtypes holds a promise for better defining these resistant cells specific to each tumour. To this end, a better understanding of TNBC heterogeneity and cancer stemness is required, and extensive genomic analysis can help to understand the disease complexity and distinguish new molecular drivers that can be targeted in the clinics. The use of persister cancer cell-targeting therapies combined with other therapies may provide a big advance to improve TNBC patients' survival.
已知三阴性乳腺癌(TNBC)亚型相较于其他乳腺癌亚型具有更具侵袭性的临床病程。针对这类乳腺癌的靶向治疗有限,患者大多接受传统的化疗和放疗,这些治疗不具有特异性,也不针对耐药细胞。因此,主要的临床挑战之一是找到能够靶向负责形成继发性肿瘤的耐药细胞群体的化合物。不同TNBC亚型的分子谱分析有望更好地定义每种肿瘤特有的这些耐药细胞。为此,需要更好地理解TNBC的异质性和癌症干性,广泛的基因组分析有助于理解疾病的复杂性,并区分可在临床上靶向的新分子驱动因素。使用针对持久性癌细胞的治疗方法与其他疗法相结合可能会在提高TNBC患者生存率方面取得重大进展。